- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Annual Issues
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Reviewers Acknowledgment
- Submit a Manuscript
- Subscription Information
- Table of Contents
Journal of Biomedicine and Biotechnology
Volume 2012 (2012), Article ID 493618, 15 pages
Various Jobs of Proteolytic Enzymes in Skeletal Muscle during Unloading: Facts and Speculations
SSC RF Institute for Biomedical Problems, RAS, Moscow, Russia
Received 12 May 2011; Revised 11 October 2011; Accepted 3 November 2011
Academic Editor: Lars Larsson
Copyright © 2012 E. V. Kachaeva and B. S. Shenkman. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Skeletal muscles, namely, postural muscles, as soleus, suffer from atrophy under disuse. Muscle atrophy development caused by unloading differs from that induced by denervation or other stimuli. Disuse atrophy is supposed to be the result of shift of protein synthesis/proteolysis balance towards protein degradation increase. Maintaining of the balance involves many systems of synthesis and proteolysis, whose activation leads to muscle adaptation to disuse rather than muscle degeneration. Here, we review recent data on activity of signaling systems involved in muscle atrophy development under unloading and muscle adaptation to the lack of support.
Functional unloading caused by prolonged weightlessness or bed rest (after trauma, etc.) leads to sufficient physiological alterations of skeletal muscles, mainly postural, as soleus. Studies on animals  and volunteers  showed that unloading leads to changes at the molecular level, which manifest in muscle mass loss and deterioration of its function.
In this paper, we paid attention mainly to the atrophy caused by hindlimb suspension, since this is the most correct experimental disuse mode, while muscle denervation, for instance, leads not only to disuse, but also to impaired trophic regulation of the muscle, which complicates atrophy data interpretation.
To study molecular processes during disuse, special models are used for animals (hindlimb unloading)  and volunteers (bed rest, dry immersion). Each of the models leads to development of a complex of structural and functional changes, as decrease of cross-sectional area and contractile activity of muscle itself and its single fibers [4####^~^~^~^~^~^####x2013;7]. There are also changes in myosin phenotype observed [8, 9] as well as enzyme activity . Such hypogravitational syndrome  is supposed to be caused by changes in concentration and activity of factors circulating in blood (glucocorticoids and anabolic steroids) . At the same time, cortisol was shown to affect muscle under disuse indirectly ; while in muscle cytosol, quite high concentration of glucocorticoid receptors was observed . Consequently, there are other mechanisms involved in muscle atrophy stimulation and development during unloading.
Muscle atrophy development under hypokinesia/hypogravity involves different signaling systems directed towards proteolysis activation and protein balance maintaining. Thus, an increase in content of components of the TGF-####^~^~^~^~^~^####x3b2;/Smads (transforming growth factor-####^~^~^~^~^~^####x3b2;) signaling pathway  and decrease of activity of phosphatidyl inositol-3-kinase (PI3####^~^~^~^~^~^####x2009;K/Akt) cascade were shown. These changes reflect activation of both proteolytic and synthetic signaling pathways in skeletal muscle . Therefore, we aimed at the analysis of the known pathways of proteolysis in postural muscles during functional unloading.
2. Main Systems of Proteolysis in Skeletal Muscles
Three catabolic pathways are known to be involved in the atrophy process during hypokinesia/hypogravity: Ca2+-dependent, lysosomal, and ATP-ubiquitin-dependent proteolytic pathways. However, these systems participate differently in muscle atrophy development caused by denervation and disuse. Thus, under disuse, activity of lysosomal proteases does not increase significantly .
Animals hindlimb suspension (HS) and human head-down bed-rest lead to an increase in mRNA of 14####^~^~^~^~^~^####x2009;kDa ubiquitin-binding enzyme, and 20S proteasome subunits [17, 18] and to an increment of ubiquitinated proteins , which proves significant contribution of ubiquitin proteasome system (UPS) in muscle atrophy under unloading.
Besides, Ca2+-dependent proteases (calpains) also play an important role in skeletal muscle atrophy under disuse [17, 20, 21], being a system of primary protein degradation, since they do not degrade proteins to amino acids or small peptides .
Complex effect of activation of different proteolytic systems results in loss of muscle structural proteins and, thus, in decrease of muscle functional properties. A number of results obtained showed that atrophic changes during a space flight or under head-down bed-rest are accompanied by decrease of total muscle protein  and myofibril proteins degradation .
We suppose that first stage of muscle protein degradation can be Ca2+-dependent proteases, since Ca2+ overloading is the first event observed in unloaded muscles, and it is calcium ions which stimulate primary myofibrils degradation. Stimuli inducing Ca2+ accumulation are not studied well. Thus, we start our review of proteolytic systems from calcium-dependent system.
Further, we will discuss proteolytic systems in details.
3. Calcium-Dependent Pathways of Proteolysis
Looking for a trigger of proteolysis researchers paid attention to Ca2+-dependent proteases. Calcium redistribution between cytoplasm and sarcoplasmic reticulum (SR) during muscle atrophy caused by different diseases was first demonstrated about 30 years ago [25, 26]. Later, it was shown that 14 days of rat HS significantly increased induced by caffeine Ca2+ efflux from soleus SR . However, myoplasm overloading with calcium was demonstrated only in 2001 by Ingalls et al.  who registered Ca2+ quantity increase at the 3rd day of rats functional unloading. Dihydropyridine-sensitive channels (DHPCs) and ryanodine receptors (RYRs) are main Ca2+ channels. DHPCs are the L-type Ca2+ channels, m.w. 165####^~^~^~^~^~^####x2009;kDa, specifically blocked by dihydropyridine . They are localized predominantly in T-tubes of muscle fibers and are activated by depolarization of fiber membrane. At that, Ca2+ enters myoplasm without consumption of ATP hydrolysis energy.
We demonstrated that DHPCs specific inhibitor, nifedipin, caused significant decrease of Ca2+ in soleus fibers during unloading . Since DHPCs are the voltage-dependent structures, they should be activated by changes of electrochemical potential at the myofiber membrane under disuse. Some authors showed membrane potential decrease in disused rat soleus [31, 32]. Six percent of decrease of membrane potential was observed at the 3rd day of animal hind limb suspension (HS) . However, potential alteration was not significant, and there were no direct evidences of membrane potential influence to Ca2+ accumulation, so the question of possible trigger of Ca2+ accumulation remains unclear.
RYR is another source of Ca2+, localized in terminal cisternae membrane near DHPCs. These channels efficacy significantly exceeds that of DHPCs. RYR main function is fast Ca2+ influx to cytosol, where calcium ions interact with troponin C stimulating mechanism of fiber contraction. RYR and DHPC are known to be connected with each other structurally and functionally in fiber T-system. RYRs are activated when interact with Ca2+-activated DHPC .
Ca2+ accumulation in myoplasm stimulates Ca2+-dependent proteolytic processes. Experiments with activators of Ca2+ transport demonstrated the increase in protein degradation , while dantrolene (specific blocker of Ca2+ exit from SR) decreased proteolysis rate .
However, Ca2+-dependent proteolysis localization is not clear, since there are a number of data supporting  and contradicting  its lysosomal localization. Though, calcium can affect indirectly lysosomal proteases like cathepsin B , and nonlysosomal ones localized in cytosol of myofibers .
In myoplasm, Ca2+ activates cystein proteases, calpains, which are divided into two groups according to their sensitivity to Ca2+: ####^~^~^~^~^~^####x3bc;- and m-calpains (calpain 1 and calpain 2); they are activated by micromolar and millimolar calcium concentrations, correspondingly. Skeletal muscles contain also calpain 3 (p94), which has common structure with calpains 1 and 2. Ca2+ dependence of p94 was proved only in 2006####^~^~^~^~^~^####x2009;. At the early stages of functional unloading, calpains are activated and redistributed from cytoplasm fraction to the membrane in slow and fast muscles .
The fact that activity of soluble and membrane fractions significantly increased after 12 hours of animal hindlimb suspension and remains high till 9th day of disuse proves that calpains take part in muscle atrophy development under hypokinesia/hypogravity . Moreover, we found twofold increase in soluble calpain fraction activity and fivefold increment of membrane fraction activity after 3 days of animal disuse  and were first to show directly that increase in [Ca2+] stimulates ####^~^~^~^~^~^####x3bc;-calpain activity, which in its turn activates m-calpains [20, 36]. Local application of Ca2+ chelator 1####^~^~^~^~^~^####x2009;,2-bis(2-aminophenoxi)ethan-N,N,N####^~^~^~^~^~^####x2032;,N####^~^~^~^~^~^####x2032;-tetraacetate (BAPTA-AM) to soleus during unloading allowed us to demonstrate directly dependence of calpain activity on [Ca2+] in vivo . Importantly, techniques for determination of calpain activity used in the works  and  registered the enzymes activity at high millimolar concentration of calcium in the incubation medium, where higher activity of all calpain molecules was observed. Increase in calpains activity under disuse can be caused by their expression intensification or by other Ca2+-independent regulators, as calpastatin. Thus, hindlimb suspension leads to pronounced decrement of calpastatin expression in soleus, while calpain 1 expression increases slightly . Activity of calpains decreased in unloaded muscle under local application of calcium chelator  can be evidence of Ca2+-dependence of regulation of calpastatin expression.
Calpains contribute about 10####^~^~^~^~^~^####x25; to disuse muscle atrophy. Their key role was demonstrated in HS experiments with mice overexpressing calpastatin, in which no reduction of muscle fiber size was observed . These results are in agreement with recent data on calpastatin expression decrement under HS . Interestingly, hypokinesia/hypogravity caused decrease of NO content leading to calpains inhibition . At that, content of neuronal NO-synthase in soleus fibers under functional unloading decreased [41, 42].
Calpains cannot degrade proteins to small peptides or amino acids and cause only withdrawal of proteins from myofibrils, making them accessible to ubiquitination. Recently, titin was found to bind calpain-3 (p94) through a p94-specific region, suggesting that titin can regulate calpain-3 activity . Calpain-3 was shown to activate expression of components of ubiquitin-proteasome system (UPS) [44####^~^~^~^~^~^####x2013;46]. P94 blocked binding of ankyrin repeats with titin molecule . Ankyrin repeats normally are translocated to the nucleus, where they activate NFkB binding with DNA, hence stimulating ubiquitin ligase expression .
Thus, calpains and UPS work jointly (Figure 1) . At that UPS, most probably, realizes final protein degradation. Close interrelation between Ca2+-dependent proteases and UPS complicates studies of their individual contribution into atrophy development under disuse.
Intracellular localization of calpains in association with titin molecule makes possible the interrelation between UPS and calpains. Calcium accumulation under disuse activates calpains, which partly degrade titin molecule or change its conformation [41, 48]. Titin not only is involved in fiber contractility, but also realizes its signaling function through phosphorylation of ubiquitin ligases (MuRF-1 and MuRF-2) localized near titin kinase domain (in M-line), which can affect the titin molecule itself [49, 50]. 14-day HS is known to significantly decrease relative content of titin in rat soleus (Table 1) [51####^~^~^~^~^~^####x2013;53]. The same decrease of titin content was observed in human soleus after 7 days of dry immersion experiment , interestingly, that titin molecule remains intact at the 3rd day of animal HS [7, 51]. These results prove that, at the early stage of disuse, titin remains intact in spite of myoplasm overloading with calcium [7, 28] and increase in calpain activity. Consequently, phosphorylation of titin bound UPS components and their low activity is maintained. Meanwhile, calpastatin overexpression in mice under disuse was shown to prevent slow-to-fast shift in myosin heavy chains (MHCs) . Probably, degradation of one of the calpain targets under disuse impairs regulation of slow MHC expression, which determines MHC phenotype transformation. Moreover, calpain 2 under HS translocates into the nucleus, where it initiates apoptosis . Thus, calpains in skeletal muscles besides their direct proteolytic activity possess also signaling properties, which are realized partly through the E3-ubiquitin ligases .
4. Ubiquitin Proteasome System
Components of ubiquitin proteasome system (UPS) [19, 55, 56] were shown to be actively synthesized under disuse [15, 17, 19, 57] and under muscle atrophy of other nature [55, 58]. Intensification of proteolytic activity is caused by increase in quantity of mRNA encoding main UPS members (polyubiquitin, ubiquitin binding enzymes, ubiquitin ligases, 20####^~^~^~^~^~^####x2009;S proteasome subunits) and following synthesis of corresponding proteins . The scheme of UPS-dependent degradation of proteins is shown at the Figure 2. Ubiquitination process needs activation of three UPS enzymes: ubiquitin-activating enzyme (E1), ubiquitin-binding enzyme (E2), and ubiquitin ligases (E3). At first ubiquitin binds to E1 (ATP-dependent process) and then translocates to E2. E3 ligases covalently bind protein substrate and then interact with E2, which carries activated ubiquitin. Ubiquitin in its turn translocates from E2 to the target protein. The process repeats till target protein binds a chain of 4-5 ubiquitin molecules. Then, the ubiquitinated protein degrades into peptides inside proteasome . E3 ligases play an important role in recognition of proteins to be degraded. E2 enzyme and E3 ligase are tissue specific, individual E2 interacts with particular E3 ligase. Usually two main markers of UPS activity are studied, atrogin-1 or muscle atrophy F-box (MAFbx) and MuRF1 (muscle RING finger protein 1) . MAFbx participates in formation of functional ligase complex. MuRF-1 binds conservative domain of titin molecule localized between titin kinase domain and titin C-terminal (in M-line) [48, 61]. This interaction is supposed to regulate metabolism of myofibrils, their trophic state, and maintains entirety of M-line region .
MAFbx is supposed to ubiquitinate and degrade MyoD  and eukaryotic factor of translation initiation 3 (eIF3) , thus playing role in muscle protein synthesis inhibition rather than in proteolysis activation in wasting muscle. MuRF-1 ubiquitinates and degrades troponin I  and myosin heavy chains .
4.1. E3 Ubiquitin Ligases under Functional Unloading
Expression rate of E3 ubiquitin ligases genes increased after denervation, immobilization, hindlimb suspension, and after 11 days of animal space flight, which demonstrated MAFbx- and MuRF-1-dependent proteolysis under disuse [15, 58, 67]. Generally, MAFbx and MuRF-1 are universal proteases participating in skeletal muscle atrophy of different kinds .
Results of studies on volunteers using biopsy of vastus lateralis revealed difference between muscle atrophy development in animal and in human, because, in human biopsy significant decrement of protein synthesis and lack of proteolysis increase were observed . At the same time, studies on volunteers during antiorthostatic head-down bed-rest showed increased MuRF-1 quantity in soleus (slow muscle), rather than in vastus lateralis (containing predominantly fast fibers) . Later, expression intensification of MAFbx and ubiquitin ligase cbl-b was found in vastus lateralis after 20 days of disuse . After 48 hours of unilateral lower limb suspension of volunteers, complete genomic analysis revealed increase in expression rate of mRNA of E3 ubiquitin ligases , also accumulation of 3-metilhistidine, product of degradation of myofibril proteins (actin and some myosin) was observed . Ten days of immobilization caused threefold increase in MuRF-1 mRNA content in quadriceps femoris, which, however, was diminished to the control level to the 21st day of unloading . We also observed changes in expression rate of ubiquitin ligases under HS of animals. Thus, we found that expression rate of MuRF-1 and MAFbx mRNA in rat soleus increased 3####^~^~^~^~^~^####x2009;.3 and 2####^~^~^~^~^~^####x2009;.1 times, correspondingly, at the 3rd day of disuse. To the 7th day of HS, this parameter decreased but was 1####^~^~^~^~^~^####x2009;.27 and 1####^~^~^~^~^~^####x2009;.52 times higher than in control (Figure 3) . The 37####^~^~^~^~^~^####x25; increase in total level of protein ubiquitination at the 4th day of functional unloading  confirms our data.
4.2. MuRF-2 and Signaling Role of E3 Ubiquitin Ligases
Recently, information appeared about functions of another E3 ubiquitin ligase, MuRF-2, which is splice variant of MuRF-1. MuRF-2 is usually found in embryonic muscle, while, in adult animals, its quantity decreased. In spite of its predominant localization in cytoplasm, partly MuRF-2 is bound to nbr1 and p62 proteins, which localize at titin molecule near M-line (Figure 4) [49, 76]. Normally, one of the main functions of this protein is stabilization of microtubules population and several proteins of sarcomeric cytoskeleton (desmin, vimentin) during myofibrillogenesis . Besides, along with MuRF-1, MuRF-2 participates in ubiquitination of myofibril proteins . It should be noticed that MuRF-2 is regulated, at least partly, by titin-dependent mechanism . Changes in spatial arrangement of titin kinase domain after denervation can cause loss of its main function. Consequently, dephosphorylated MuRF-2 dissociates from titin and translocates into the nucleus, where it forces out serum response factor protein (SRF), which is responded for c-fos-mediated stimulation of protein synthesis, cytoskeletal molecules expression, and expression of several growth factors. Our preliminary data showed MuRF-2 translocation to the nucleus and its increased expression under disuse. Thus, 7 days of HS caused increase in MuRF-2 concentration as in myoplasm (from ####^~^~^~^~^~^####x2009;r.u. to ####^~^~^~^~^~^####x2009;r.u., according to western blot densitometry data), so in nucleus (from to r.u.) (unpublished data). Increment of MuRF-2 protein quantity increased further being almost twice as higher at the 14th day of disuse in myoplasm and nucleus. Thus, disuse induces synthesis and translocation of MuRF-2 into the nucleus. According to the data of Lange et al. , it seems that titin conformational changes under unloading should cause degradation of signaling complex, associated with titin kinase domain, and allow MuRF-2 migration to the nucleus. Such change in protein conformation was observed after 2 days of unloading , while data of other authors did not reveal any changes in titin content at the 3rd day of disuse [7, 53]. MuRF-2 concentration in nucleus fraction of rat soleus did not change, as compared to control, at the 3rd day of HS. However, data exist, which demonstrate titin stability at the 3rd day of HS; only after 7 days of HS, titin was degraded noticeably (Table 1). These data confirm that at the early stage of unloading myoplasm overloading with calcium [7, 28] and calpains activation cannot stimulate titin proteolysis and, thus, ubiquitin ligases dephosphorylation. Therefore, two triggers of MuRF-1 and MuRF-2 dephosphorylation can exist: Ca2+-dependent calpain activation, which initiates myofibril proteins disorganization, and titin conformational changes caused by titin sensitivity to mechanical strain. Further studies are necessary to answer the question.
Normally, MuRF-1 and MuRF-2 expression is more pronounced in fast fibers (II type), while, in mice MuRF-1 and MuRF-2 knockouts, and especially in double knockouts (MuRF-1 and MuRF-2), number of fast soleus fibers is significantly decreased. At that, lack of MuRF-1 noticeably prevented atrophy of II type fibers of tibialis anterior . In double knockouts expression of myozenin-1 (calsarcin-1), an endogenous inhibitor of calcineurin/NFAT signaling pathway was blocked. Obviously, nucleus localization of MuRF-1 and MuRF-2 stimulates calsarcin expression leading to stabilization of fast phenotype of muscle fiber. Mice MuRF-1 knockouts did not show significant atrophy of soleus after 10 days of HS, while fatigue characteristics were more pronounced, posttetanic potentiation was not as increased as in mice of wild type . The authors suppose possible MuRF-1 influence on intensified processes of phosphorylation of regulatory myosin light chains [81, 82].
Signaling roles of E3 ligases and some of their targets are known now. Thus, MAFbx ubiquitinates MyoD and eIF3####^~^~^~^~^~^####x2009;[63, 64]. Taking part in eIF3 ubiquitination MAFbx plays important role in regulation of reciprocal interaction between anabolic and catabolic signaling pathways. Troponin I  and myosin heavy chains  are the targets of MuRF-1, playing an important role in deterioration of muscle contractility.
Interestingly, ubiquitination of histone deacetylase of II type is supposed to be one of the mechanisms of fast-to-slow transformation of myosin phenotype, which is supported by decrease of slow myosin expression under application of proteasome inhibitor MG132####^~^~^~^~^~^####x2009;. At that, exact E3 ubiquitin ligase participating in this phenomenon remains unknown.
Data discussed above showed that direct ubiquitination and indirect participation of E3 ubiquitin ligases in signaling processes makes them important components of central signaling mechanisms in muscle fiber. Unfortunately, today, there is not enough information to understand completely role of E3 ligases in processes of transformation or stabilization of myosin phenotype and concomitant events.
4.3. Regulation of Ubiquitin Ligases Expression
In spite of some progress in understanding of activation and possible functions of ubiquitin proteasome system, trigger mechanism stimulating its activity, particularly activity of E3 ubiquitin ligases, remains to be determined.
Transcription regulation factor NFkB, which is a mediator of cytokine TNF####^~^~^~^~^~^####x3b1; (tumor necrosis factor ####^~^~^~^~^~^####x3b1;) during cachexia and inflammation, plays important role in skeletal muscle atrophy. TNF####^~^~^~^~^~^####x3b1;, in its turn, induces muscle fibers apoptosis and specific transcription mechanism, which blocks IGF-1-induced anabolic process . Inactivated NFkB forms complex with IkB in myoplasm. TNF####^~^~^~^~^~^####x3b1; stimulates IkB kinase, which phosphorylates IkB leading to ubiquitination and degradation of proteins of this family. NFkB then moves to the nucleus and binds to sense sequence of DNA, thus regulating transcription of NFkB-dependent genes. TNF####^~^~^~^~^~^####x3b1;-induced NFkB activation is known to suppress regulatory muscle factor MyoD at posttranscriptional level . In 2004, Cai and colleagues demonstrated at least partial relation of muscle atrophy caused by cachexia, with activation of MuRF-1, but not with MAFbx . This discovery stimulated study of action mechanism of NFkB system in muscles under disuse.
It was found that atrophy caused by functional unloading in rodents can be partly explained by TNF####^~^~^~^~^~^####x3b1;-independent activation of NFkB. Seven days of HS in soleus stimulated DNA-binding activity of NFkB and led to an increase of reporter proteins p-50, c-Rel, and nuclear IkB protein Bcl-3####^~^~^~^~^~^####x2009;[86, 87]. Akt activation and TNF####^~^~^~^~^~^####x3b1; expression did not increase as it happened during cachexia. These facts proved mechanism of atypical activation of NFkB during atrophy caused by functional unloading. This mechanism was called trans-regulation . Importantly, NFkB pathway was not activated under disuse in fast muscles . Possible targets of trans-activation of NFkB under hypokinesia were found recently . Disuse was shown to induce NFkB-dependent increase in expression rate of ubiquitin ligases MAFbx and Nedd4. Analysis of 5####^~^~^~^~^~^####x2032;-flanking sites of genes of these ligases allowed finding numerous potential binding sites of NFkB. Moreover, 4EBP1, FoxO3a, and cathepsin L (lysosomal enzyme, which degrades membrane proteins) are also possible targets of NFkB; their expression was increased under disuse atrophy . At the same time, in mice overexpressing IKK####^~^~^~^~^~^####x3b2;, specific component of muscle signaling pathway, 15-fold increase in NFkB activity was shown to stimulate MuRF-1 activity. In the experiments with C2####^~^~^~^~^~^####x2009;C12 culture of myotubes, 4.6-fold rise of MuRF-1 promoter activity was found, which was blocked by IkB####^~^~^~^~^~^####x3b1;-SR transfection. Thus, as opposed to disuse-stimulated atrophy, during TNF-####^~^~^~^~^~^####x3b1;-dependent atrophy, induction of MuRF-1 transcription was observed . These data reveal predominant NFkB-mediated activation of MAFbx under disuse, while MuRF-1 is stimulated by NFkB during other kinds of atrophy. Since MuRF-1 is known to be activated under muscle wasting, there must be other mechanisms which activate MuRF-1 expression. Thus, transcription regulators FoxO1 and FoxO3 were shown to activate MuRF-1 expression [89, 90].
6. FoxO and Myostatin
Fox factors of transcription regulation have got their name according to their structure (forkhead box) , and, in mammals, they are called FoxO (other), because of different structure of their DNA-binding domains; among them FoxO1, FoxO3####^~^~^~^~^~^####x2009;a, FoxO4, and FoxO6####^~^~^~^~^~^####x2009;.
FoxO factors participate in a number of physiological and pathological processes, aging and cancer, for instance . Proteins of this family being phosphorylated by Akt can bind chaperone 14-3-3 in cytoplasm, which leads to loss of their capacity for expression regulation . Model of atrophy on myotube culture revealed decrease of activity of IGF-1/insulin/phosphatidilinositol-3-kinase (PI3####^~^~^~^~^~^####x2009;K/Akt) signaling pathway, which caused initiation of FoxO transcription factors and MAFbx induction (Figure 5) . Importantly, FoxO3 directly interacts with MAFbx promoter stimulating expression of the proteases genes, which leads to atrophy of myotubes in culture and animal muscle fibers . Since PI3####^~^~^~^~^~^####x2009;K/Akt is known to suppress MuRF-1 expression, so FoxO participates also in regulation of MuRF-1 activity . Recently, FoxO1 was shown to negatively affect expression of myosin heavy chain of type I , which confirms important role of FoxO factors in skeletal muscle atrophy.
Balance between protein synthesis and proteolysis involves not only Akt signaling pathway, but also FoxO-dependent cascade, which includes activation of 4EBP1 (protein binding eukaryotic factors 4####^~^~^~^~^~^####x2009;E) and inhibition of mTOR. At that, FoxO is regulated by different posttranslational modifications, as phosphorylation, acetylation, mono- and polyubiquitination . Some of these modifications are independent on Akt; hence, they also can be involved into muscle atrophy development under stress.
Akt-FoxO signaling pathway is known to interact with IKK-NFkB system during muscle atrophy development. Thus, inflammatory cytokine TNF####^~^~^~^~^~^####x3b1; activating NFkB pathway blocks sensitivity to insulin and inhibits IGF-1 pathway [95####^~^~^~^~^~^####x2013;97]. Moreover, interaction between these two signaling systems was confirmed by the results of the study on IKK####^~^~^~^~^~^####x3b2; knockout mice, whose were insensitive to muscle atrophy induced by denervation, while demonstrated excessive Akt phosphorylation .
Search for triggering mechanism initiating dephosphorylation of Akt and FoxO and stimulating ubiquitin ligases expression under disuse allowed to find process of degradation of IRS-I (insulin receptor-I), which is intermediate in IGF-1/PI3/Akt signaling cascade. IRS-I content and its phosphorylation level in and Ser789 sites decreased significantly after 14 days of HS . Later, it was found that IRS-I is degraded by ubiquitin ligase cbl-b, which expression is increased noticeably under disuse . Cbl-b expression is regulated during membrane process of lipid peroxidation.
As was shown previously, FoxO factors mediate ubiquitin ligases activation also through myostatin . The latter blocks IGF-1/PI3####^~^~^~^~^~^####x2009;K/Akt pathway, which activates FoxO1, thus stimulating MAFbx expression . Data on regulation of myostatin expression by FoxO1 showed that myostatin signaling pathway is related to Akt-FoxO cascade . Mature myostatin protein forms active dimers, which bind activin receptors on the cell surface stimulating phosphorylation of Smad2 and Smad3 and their interaction with Smad4. Such complex is a transcription regulation factor, which can penetrate the cell and induce expression of any gene flanked with corresponding sequence. In other words, myostatin blocks myoblasts growth in the cell, inhibiting thus the expression of myogenic factors as MyoD and p21####^~^~^~^~^~^####x2009;. Myostatin negatively regulates activation and self-renewal of cells and, probably, participates in process of the satellite cells silencing . Thus, myostatin activity maintenance under disuse, possibly, promotes maintenance of low level of myofibers renewal and prevents potential increase in satellite cells proliferation and fusion.
At the same time, Smad proteins can recognize CAGAC DNA sequence but possess low affinity to it, so to interact with DNA Smad proteins need some DNA binding co-factors, which can help to recognize and regulate target genes . Such mediators are proteins of the FoxO family . Besides, Smads inhibitor, TGIF, was shown to be activated earlier than muscle mass loss becomes noticeable.
7. Autophagy: Lysosomal Proteins Degradation
Lysosomes are the cell organelles responsible for removal of other organelles and aggregated proteins. Autophagy is an integral property of muscle cells, which is confirmed by huge number of autophagosomes in humans with myopathies caused by different diseases or during pharmacological inhibition of lysosomal function by chloroquine, for instance . However, lysosomal enzymes are differently activated during atrophy induced by denervation  and unloading . According to biochemical and electron microscope data, lysosomal degradation of proteins is responsible mainly for denervation-induced atrophy [78, 107####^~^~^~^~^~^####x2013;109]. These results are in accordance with the data that chloroquine practically cannot block proteolysis during hypokinesia/hypogravity but inhibits it during soleus denervation . Moreover, significant activation of Ca2+-dependent carbothiolic proteases and decrease of total cathepsin B and D activity were observed under disuse stimulated by hindlimb unloading, while denervation-induced disuse caused the highest activity of the cathepsins . At the same time, recently, catepsin L quantity was shown to be increased during HS [58, 111]. Role of catepsin L is unknown. Thus, increment of certain catepsins concentration proves some lysosomal system activation during denervation-induced atrophy but does not have significant contribution of lysosomes to HS-induced atrophy . Catepsins are known to be inactivated at neutral pH in cytoplasm. Proteolysis with catepsins is carried out inside the lysosomes; thus, they cannot degrade myofibril proteins despite of their activation. Therefore, lysosomal system contribution into catabolism of myofibril proteins during atrophy is not sufficient .
mTOR and PI3####^~^~^~^~^~^####x2009;K/Akt signaling systems are also involved in microtubules autophagy . Recently, the results were obtained demonstrating coordination between lysosomal system and UPS during atrophy [114, 115]. Therefore, some genes related with autophagy, as well as MAFbx gene, are controlled by FoxO3 regulatory factor, and thus expression of FoxO1 and FoxO3 can be necessary for lysosomal proteolysis induction mediated by activation of ubiquitin ligases MAFbx and MuRF-1 in cell culture and in vivo [91, 93]. At that, it is still unknown whether such interaction of these proteolytic systems takes place in skeletal muscles of animals under disuse.
Caspases are known to cleave actomyosin to 14####^~^~^~^~^~^####x2009;kDa actin fragments, as was shown in culture of skeletal muscle cells on the model of serum deprivation . Caspase-3 contribution to protein degradation by UPS in culture was 125####^~^~^~^~^~^####x25;. The observed by Du et al. actomyosin cleavage was blocked by specific caspase-3 inhibitor. Cleaved actin fragments were also found in rat muscles after diabetes and chronic uremia . Caspases were shown to be activated during rat hindlimb unloading [117, 118]. Interestingly, at the 5th day of HS, only caspase-3 content increased, while, at the 10th day of disuse, caspases-6 and 9 were activated. These data confirm that caspase-3 activates as through mitochondria-independent, so through mitochondria-dependent pathway during unloading caused by HS. However, the entire mechanism of mitochondria-independent caspase regulation needs further investigation. Physiological role of caspase content increment can be the myonuclei number regulation through apoptosis, which leads to synthesis activity decrease. Though, it was found that caspase-3 increase caused decrease in myonuclei number  and stimulated DNA fragmentation at the 14th day of HS . Mechanisms of this phenomenon are also remained unclear.
9. Muscle Atrophy Is the Balance between Signaling Systems Involved in Regulation of Protein Synthesis and Proteolysis
Alterations of structure and function of skeletal muscle under functional unloading, so called, muscle plasticity, are caused not only by increment of muscle proteins degradation. It is better to say that disuse atrophy is the result of shift of the balance between protein synthesis and proteolysis towards increase in proteolysis and decrease of synthesis intensity. Main signaling system regulating protein synthesis in muscles is the Akt/mTOR pathway, which is activated when IGF-1 (insulin-like growth factor-1) binds with its receptor on myofiber membrane. This signaling cascade is responsible for stimulation of protein synthesis in skeletal muscle fibers realizing its effect particularly through stimulation of proliferation and fusion of satellite cells (Figure 5) . mTOR (mammalian target of rapamycin) is a part of two multiprotein complexes, one of which is mTORC1 (sensitive to rapamycin). mTORC1 activates S6####^~^~^~^~^~^####x2009;K and 4EBP, through which Akt-FoxO signal is realized. mTOR effect on translation process and protein synthesis is realized through TORC1-dependent phosphorylation of ribosomal S6 kinases (S6####^~^~^~^~^~^####x2009;K1 and S6####^~^~^~^~^~^####x2009;K2) and 4EBP, a repressor of a cap-binding protein eIF4####^~^~^~^~^~^####x2009;E. S6####^~^~^~^~^~^####x2009;K1 is an important component of Akt cascade, which is confirmed by experiments on mice S6####^~^~^~^~^~^####x2009;K1 knockouts. Those mice had very small fibers, and could not respond to activated Akt and IGF-1####^~^~^~^~^~^####x2009;. Thus, protein synthesis intensification through PI3####^~^~^~^~^~^####x2009;K/Akt/mTOR mechanism is realized by means of activation of S6####^~^~^~^~^~^####x2009;K1, eukaryotic factor of translation initiation 4####^~^~^~^~^~^####x2009;E (eIF4####^~^~^~^~^~^####x2009;E), and inhibition of translation regulator 4EBP1. At the same time, IGF-1/PI3####^~^~^~^~^~^####x2009;K/Akt pathway prevents atrophy development by inhibition (dephosphorylation by Akt) of transcription regulation factors FoxO1####^~^~^~^~^~^####x2009;-3, stimulating their transition from nucleus to cytoplasm . Activity of IGF-1 plays an important role during functional unloading, since ability of muscle cells to bind insulin increased noticeably under disuse. At that, total quantity of insulin receptors did not change . At the same time, activity of PI3####^~^~^~^~^~^####x2009;K/Akt signaling cascade, which plays role of central regulator between insulin and IGF-1 receptor, and activated synthetic pathways in muscle, were shown to be diminished significantly [123, 124]. Moreover, it was clearly demonstrated that c-Jun NH2-terminal kinase (JNK) significantly increased after 10 days of rat HS, as in predominantly fast [125, 126], so in predominantly slow muscles , on the models of animal HS [125, 127], cast immobilization , and denervation . Independently of the model used increment in JNK level evidences that IRS-1 protein is phosphorylated, Akt activity is suppressed, and insulin resistance develops in the wasting muscle. Therefore, activation of PI3####^~^~^~^~^~^####x2009;K/Akt signaling pathway is important for disused muscle reloading. Nevertheless, it is not the only way of protein synthesis intensification. Eukaryotic initiation factor 4####^~^~^~^~^~^####x2009;E (eIF4####^~^~^~^~^~^####x2009;E), one of the components of eIF4####^~^~^~^~^~^####x2009;F complex interacts with eIF3 complex, which regulates assembling of 43####^~^~^~^~^~^####x2009;S preinitiation complex (PIC) . eIF3 directly captures 40####^~^~^~^~^~^####x2009;S ribosomal subunit stimulating its interaction with Met-tRNA-eIF2-GTP complex and with eIF1. Due to interaction of eIF3 and eIF4####^~^~^~^~^~^####x2009;E-mRNA, mRNA binds 43####^~^~^~^~^~^####x2009;S ribosomal complex forming 48####^~^~^~^~^~^####x2009;S complex, which initiates synthesis of muscle proteins. Studies revealed 13 different subunits of eIF3 complex with molecular mass varying from 170 to 25####^~^~^~^~^~^####x2009;kDa. Five of these subunits form the main nucleus of the complex, and others have regulatory function. Role of one of these subunits, eIF3-f, is not known well, though in yeasts and coronaviruses, decrease of eIF3-f quantity leads to significant reduction of total protein content in dividing cells and to decrement of cytokines IL-6 and IL-8####^~^~^~^~^~^####x2009;. IL-6, in its turn, is an essential factor of development of skeletal muscle hypertrophy mediated by proliferating satellite cells . In humans, eIF3-f decrease is related to tumor development, while its overexpression suppresses cell growth and leads to apoptosis stimulation .
Small quantity of eIF3-f is found in myoblasts of skeletal muscles. Its concentration increases significantly during terminal differentiation and remains at the same level in adult muscle. Interestingly, eIF3-f binds MAFbx in skeletal muscle, which explains, probably, protein synthesis decrease during muscle atrophy of different nature . MAFbx is known to stimulate polyubiquitination of eIF3-f with its following degradation by 26####^~^~^~^~^~^####x2009;S proteasome. Therefore, decrease of MAFbx will lead to maintaining of eIF3-f level.
eIF3-f directly interacts with mTOR and S6####^~^~^~^~^~^####x2009;K1 stimulating assembling of preinitiation complex of translation of specific mRNA encoding proteins, which participate in muscle hypertrophy. According to Csibi####^~^~^~^~^~^####x2019;s data , inactive hypophosphorylated form of S6####^~^~^~^~^~^####x2009;K1 is physically bound to eIF3-f in the site of MAFbx and ubiquitin binding. Hence, MAFbx-initiated eIF3-f degradation must lead to S6####^~^~^~^~^~^####x2009;K1 inhibition during atrophy. Though it is still unknown whether MAFbx interacts with free-eIF3-f molecule or with the molecule bound to S6####^~^~^~^~^~^####x2009;K1. Thus, it is difficult to suppose in which direction shifts the balance between eIF3-f binding with the two ligands under disuse and which factors can affect this balance.
MAFbx has been considered as active proteolytic system member under functional unloading, while recent data confirm predominant role of MAFbx in suppression of protein synthesis at the stage of mRNA translation in case of its interaction with eIF3-f, or at the level of FoxO and MyoD activity inhibition [64, 129]. Thus, MAFbx should be considered as muscle atrophy marker rather than an index of proteolysis.
10. Ways to Suppress Expression of Ubiquitin Ligases under Functional Unloading
Chronic passive stretch of the muscle is supposed to be one of the most effective experimental approaches to prevent muscle atrophy . First experiments with stretch combined with HS revealed marked protein synthesis intensification, while proteolysis, at least, during first 7 days, remained unchanged . Meanwhile, our study of stretch combined with HS for 7 days showed twofold (and after 14 days of disuse with stretch threefold) increase in MuRF-1 and MAFbx expression in soleus . At the same time, these effects were accompanied by significant rise of IGF-1 expression in soleus, which allows maintaining of proteolysis-synthesis balance in the stretched unloaded muscle with high UPS expression level. IGF-1 expression activation itself can promote decrease in the expression rate of ubiquitin ligases through the induction of Akt phosphorylation, as was described in .
Moreover, it was shown also that the stretch-induced dynamic redistribution of p94 is dependent on its protease activity and essential to protect muscle from degeneration, particularly under physical stress . Though, we do not know whether the same phenomenon takes place during the unloaded muscle stretch.
Another possible way of protein synthesis maintaining in unloaded muscle can be injection of amino acids. Recently, it was shown that per oral administration of leucine amino acid during rat soleus immobilization significantly decreased expression rate of E3 ubiquitin ligases . Mechanism of this phenomenon remains unclear.
Dependence of FoxO3 migration to the nucleus and inhibition of expression of E3 ubiquitin ligases on protective systems of myofibers was found in the experiments with plasmid transfection encoding heat shock protein 70 (HSP70). Four days of immobilization after such transfection revealed decrement of E3 ubiquitin ligases expression mediated by FoxO3 dephosphorylation . We observed decrease of MuRF-1 and MAFbx expression in rat soleus under HS combined with application of NO donor, L-arginine. Evidently, experimental intensification of NO production inhibited ubiquitin ligases expression .
11. Conclusion: Hypogravitational Atrophy of Skeletal Muscle Is a Sustainable Adaptation of Signaling Systems
Signaling systems in the cell and in fibers of skeletal muscle, in particular, are joined into extremely complex net. Change of one of its components will certainly lead to alteration of many others. At that, activity of all chains involved in the net is directed differently; therefore, any imbalance of the system should initiate processes of homeostasis maintaining. Functional unloading leads to atrophy of skeletal muscles, which manifests in increased proteolysis leading to decrease of fiber size, muscle mass loss, function deterioration, loss of Ca2+ sensitivity, and so forth. However, under disuse, balance between protein synthesis and proteolysis shifts so that muscle adapts to the altered circumstances. This conclusion is supported by accumulated knowledge about activity of signaling systems, which take part in proteolysis and synthesis of muscle proteins, as NFkB, for instance. Thus, under disuse, NFkB is activated independently of TNF####^~^~^~^~^~^####x3b1; (decreasing IGF-1-dependent pathway), which may be important, because, in this case, a number of factors blocking PI3####^~^~^~^~^~^####x2009;K/Akt pathway and protein synthesis are activated. Thus, unchanged Akt level allows keeping phosphorylation level of FoxO3 and restraining the latter in myoplasm.
At the same time, NFkB does not stimulate MuRF-1 activity during hypokinesia/hypogravity , which can limit in some way total level of ubiquitin ligases activity. Consequently, predominant role of MAFbx in suppression of synthetic processes in muscle and NFkB transactivation under disuse prove adaptation of the muscle to functional unloading, rather than its negative reaction to lack of basement.
Thus, it is clear now that skeletal muscles do not degrade under disuse, they adapt to altered circumstances in a way different from that of atrophy development caused by other stimuli. Mechanism of development of skeletal muscle adaptation is extremely complicated and needs further studies to reveal key regulators, which can be affected further in order to prevent development or decrease of muscle atrophy intensity.
This work was supported by RFBR Grant 11####^~^~^~^~^~^####x2009;-04-01769####^~^~^~^~^~^####x2009;a.
- D. B. Thomason and F. W. Booth, “Atrophy of the soleus muscle by hindlimb unweighting,” Journal of Applied Physiology, vol. 68, no. 1, pp. 1–12, 1990.
- V. J. Caiozzo, “Plasticity of skeletal muscle phenotype: mechanical consequences,” Muscle and Nerve, vol. 26, no. 6, pp. 740–768, 2002.
- E. R. Morey-Holton and R. K. Globus, “Hindlimb unloading rodent model: technical aspects,” Journal of Applied Physiology, vol. 92, no. 4, pp. 1367–1377, 2002.
- K. Yamashita-Goto, R. Okuyama, M. Honda et al., “Maximal and submaximal forces of slow fibers in human soleus after bed rest,” Journal of Applied Physiology, vol. 91, no. 1, pp. 417–424, 2001.
- L. Stevens, Y. Mounier, X. Holy, and M. Falempin, “Contractile properties of rat soleus muscle after 15 days of hindlimb suspension,” Journal of Applied Physiology, vol. 68, no. 1, pp. 334–340, 1990.
- A. I. Grigoriev and B. S. Shenkman, “Skeletal muscle during unloading,” Vestn. Russ. Acad. Sci. In Russian, vol. 78, no. 4, pp. 337–345, 2008.
- E. V. Ponomareva, V. V. Kravtsova, E. V. Kachaeva et al., “Contractile properties of the isolated rat musculus soleus and single skinned soleus fibers at the early stage of gravitational unloading: facts and hypotheses,” Biofizika, vol. 53, no. 6, pp. 1087–1094, 2008 (Russian).
- G. H. Templeton, M. Padalino, and J. Manton, “Influence of suspension hypokinesia on rat soleus muscle,” Journal of Applied Physiology Respiratory Environmental and Exercise Physiology, vol. 56, no. 2, pp. 278–286, 1984.
- F. Haddad, G. R. Adams, P. W. Bodell, and K. M. Baldwin, “Isometric resistance exercise fails to counteract skeletal muscle atrophy processes during the initial stages of unloading,” Journal of Applied Physiology, vol. 100, no. 2, pp. 433–441, 2006.
- A. I. Grigoriev, I. B. Kozlovskaia, and B. S. Shenkman, “The role of support afferents in organisation of the tonic muscle system,” Rossiiskii Fiziologicheskii Zhurnal Imeni I.M. Sechenova, vol. 90, no. 5, pp. 508–521, 2004.
- H. Vandenburgh, J. Chromiak, J. Shansky, M. del Tatto, and J. Lemaire, “Space travel directly induces skeletal muscle atrophy,” The FASEB Journal, vol. 13, no. 9, pp. 1031–1038, 1999.
- J. M. Steffen and X. J. Musacchia, “Spaceflight effects on adult rat muscle protein, nucleic acids, and amino acids,” American Journal of Physiology, vol. 247, no. 16, pp. R728–R732, 1984.
- S. R. Jaspers and M. E. Tischler, “Metabolism of amino acids by the atrophied soleus of tail-casted, suspended rats,” Muscle & Nerve, vol. 9, pp. 554–561, 1986.
- P. Zhang, M. Yang, H. Liu, L. Li, and X. Chen, Book of Abstracts of the 16th IAA Humans in Space Symposium, pp.53, 2007.
- S. C. Bodine, T. N. Stitt, M. Gonzalez et al., “Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo,” Nature Cell Biology, vol. 3, no. 11, pp. 1014–1019, 2001.
- D. F. Goldspink, A. J. Morton, P. Loughna, and G. Goldspink, “The effect of hypokinesia and hypodynamia on protein turnover and the growth of four skeletal muscles of the rat,” Pflugers Archiv European Journal of Physiology, vol. 407, no. 3, pp. 333–340, 1986.
- D. Taillandier, E. Aurousseau, D. Meynial-Denis et al., “Coordinate activation of lysosomal, Ca2+-activated and ATP-ubiquitin-dependent proteinases in the unweighted rat soleus muscle,” Biochemical Journal, vol. 316, no. 1, pp. 65–72, 1996.
- M. L. Urso, A. G. Scrimgeour, Y. W. Chen, P. D. Thompson, and P. M. Clarkson, “Analysis of human skeletal muscle after 48 h immobilization reveals alterations in mRNA and protein for extracellular matrix components,” Journal of Applied Physiology, vol. 101, no. 4, pp. 1136–1148, 2006.
- M. Ikemoto, T. Nikawa, S. Takeda et al., “Space shuttle flight (STS-90) enhances degradation of rat myosin heavy chain in association with activation of ubiquitin-proteasome pathway,” The FASEB Journal, vol. 15, no. 7, pp. 1279–1281, 2001.
- D. L. Enns, T. Raastad, I. Ugelstad, and A. N. Belcastro, “Calpain/calpastatin activities and substrate depletion patterns during hindlimb unweighting and reweighting in skeletal muscle,” European Journal of Applied Physiology, vol. 100, no. 4, pp. 445–455, 2007.
- J. G. Tidball and M. J. Spencer, “Expression of a calpastatin transgene slows muscle wasting and obviates changes in myosin isoform expression during murine muscle disuse,” Journal of Physiology, vol. 545, no. 3, pp. 819–828, 2002.
- D. E. Goll, V. F. Thompson, H. Li, W. Wei, and J. Cong, “The calpain system,” Physiological Reviews, vol. 83, no. 3, pp. 731–801, 2003.
- J. M. Steffen and X. J. Musacchia, “Disuse atrophy, plasma corticosterone, and muscle glucocorticoid receptor levels,” Aviation Space and Environmental Medicine, vol. 58, no. 10, pp. 996–1000, 1987.
- D. B. Thomason, R. E. Herrick, D. Surdyka, and K. M. Baldwin, “Time course of soleus muscle myosin expression during hindlimb suspension and recovery,” Journal of Applied Physiology, vol. 63, no. 1, pp. 130–137, 1987.
- A. Martonosi, A. R. de Boland, R. Boland, J. M. Vanderkooi, and R. A. Halpin, “The mechanism of Ca transport and the permeability of sarcoplasmic reticulum membranes,” Recent Advances in Studies on Cardiac Structure and Metabolism, vol. 4, pp. 473–494, 1974.
- S. Verjovski-Almeida and G. Inesi, “Rapid kinetics of calcium ion transport and ATPase activity in the sarcoplasmic reticulum of dystrophic muscle,” Biochimica et Biophysica Acta, vol. 558, no. 1, pp. 119–125, 1979.
- L. Stevens and Y. Mounier, “Ca2+ movements in sarcoplasmic reticulum of rat soleus fibers after hindlimb suspension,” Journal of Applied Physiology, vol. 72, no. 5, pp. 1735–1740, 1992.
- C. P. Ingalls, G. L. Warren, and R. B. Armstrong, “Intracellular Ca2+ transients in mouse soleus muscle after hindlimb unloading and reloading,” Journal of Applied Physiology, vol. 87, no. 1, pp. 386–390, 1999.
- B. Macintosh, A. McComas, and P. Gardiner, Skeletal Muscle: Form and Function, Human Kinetics, Champaign, Ill, USA, 2005.
- A. M. Mukhina, A. V. Zhelezniakova, I. N. Kitina, B. S. Shenkman, and T. L. Nemirovskaia, “NFATc1 and slow-to-fast shift of myosin heavy chain isoforms under functional unloading of the rat m. soleus,” Biofizika, vol. 51, no. 5, pp. 918–923, 2006.
- S. Pierno, J. F. Desaphy, A. Liantonio et al., “Change of chloride ion channel conductance is an early event of slow-to-fast fibre type transition during unloading-induced muscle disuse,” Brain, vol. 125, no. 7, pp. 1510–1521, 2002.
- I. I. Krivoĭ, V. V. Kravtsova, E. G. Altaeva et al., “Decrease in the electrogenic contribution of Na,K-ATPase and resting membrane potential as a possible mechanism of calcium ion accumulation in filaments of the rat musculus soleus subjected to the short-term gravity unloading,” Biofizika, vol. 53, no. 6, pp. 1051–1057, 2008 (Russian).
- R. J. Zeman, T. Kameyama, and K. Matsumoto, “Regulation of protein degradation in muscle by calcium. Evidence for enhanced nonlysosomal proteolysis associated with elevated cytosolic calcium,” The Journal of Biological Chemistry, vol. 260, no. 25, pp. 13619–13624, 1985.
- J. E. Desmedt and K. Hainaut, “Regulation of ionized calcium in the cytosol of muscle cells during rest: action of dantrolene on the sarcoplasmic reticulum,” The Journal of Physiology, vol. 257, pp. 87–107, 1976.
- H. P. Rodemann, L. Waxman, and A. L. Goldberg, “The stimulation of protein degradation in muscle by Ca2+ is mediated by prostaglandin E2 and does not require the calcium-activated protease,” The Journal of Biological Chemistry, vol. 257, no. 15, pp. 8716–8723, 1982.
- B. E. García Díaz, S. Gauthier, and P. L. Davies, “Ca2+ dependency of calpain 3 (p94) activation,” Biochemistry, vol. 45, no. 11, pp. 3714–3722, 2006.
- D. L. Enns and A. N. Belcastro, “Early activation and redistribution of calpain activity in skeletal muscle during hindlimb unweighting and reweighting,” Canadian Journal of Physiology and Pharmacology, vol. 84, no. 6, pp. 601–609, 2006.
- B. S. Shenkman and T. L. Nemirovskaya, “Calcium-dependent signaling mechanisms and soleus fiber remodeling under gravitational unloading,” Journal of Muscle Research and Cell Motility, vol. 29, no. 6–8, pp. 221–230, 2008.
- X.-W. Ma, Q. Li, P.-T. Xu, L. Zhang, H. Li, and Z.-B. Yu, “Tetanic contractions impair sarcomeric Z-disk of atrophic soleus muscle via calpain pathway,” Molecular and Cellular Biochemistry, vol. 354, no. 1-2, pp. 171–180, 2011.
- Y. Lomonosova, G. R. Kalamkarov, A. E. Bugrova, et al., “Protective effect of L-arginin on soleus proteins under functional unloading,” Biochemistry, vol. 76, no. 5, pp. 571–580, 2011.
- J. G. Tidball, E. Lavergne, K. S. Lau, M. J. Spencer, J. T. Stull, and M. Wehling, “Mechanical loading regulates NOS expression and activity in developing and adult skeletal muscle,” American Journal of Physiology, vol. 275, no. 1, pp. C260–C266, 1998.
- A. Moukhina, B. Shenkman, D. Blottner et al., “Effects of support stimulation on human soleus fiber characteristics during exposure to “dry” immersion,” Journal of Gravitational Physiology, vol. 11, no. 2, pp. P137–P138, 2004.
- H. Sorimachi, K. Kinbara, S. Kimura et al., “Muscle-specific calpain, p94, responsible for limb girdle muscular dystrophy type 2A, associates with connectin through IS2, a p94-specific sequence,” The Journal of Biological Chemistry, vol. 270, no. 52, pp. 31158–31162, 1995.
- R. M. Murphy, E. Verburg, and G. D. Lamb, “Ca2+ activation of diffusible and bound pools of μ-calpain in rat skeletal muscle,” The Journal of Physiology, vol. 576, no. 2, pp. 595–612, 2006.
- I. J. Smith and S. L. Dodd, “Calpain activation causes a proteasome-dependent increase in protein degradation and inhibits the Akt signalling pathway in rat diaphragm muscle,” Experimental Physiology, vol. 92, no. 3, pp. 561–573, 2007.
- L. Laure, N. Danièle, L. Suel et al., “A new pathway encompassing calpain 3 and its newly identified substrate cardiac ankyrin repeat protein is involved in the regulation of the nuclear factor-B pathway in skeletal muscle,” The FEBS Journal, vol. 277, no. 20, pp. 4322–4337, 2010.
- M. K. Miller, M. L. Bang, C. C. Witt et al., “The muscle ankyrin repeat proteins: CARP, ankrd2/Arpp and DARP as a family of titin filament-based stress response molecules,” Journal of Molecular Biology, vol. 333, no. 5, pp. 951–964, 2003.
- K. S. Litvinova, I. M. Vikhlyantsev, I. B. Kozlovskaya, Z. A. Podlubnaya, and B. S. Shenkman, “Effects of artificial support stimulation on fiber and molecular characteristics of soleus muscle in men exposed to 7-day dry immersion,” Journal of Gravitational Physiology, vol. 11, no. 2, pp. P131–P132, 2004.
- S. Lange, F. Xiang, A. Yakovenko et al., “Cell biology: the kinase domain of titin controls muscle gene expression and protein turnover,” Science, vol. 308, no. 5728, pp. 1599–1603, 2005.
- T. Centner, J. Yano, E. Kimura et al., “Identification of muscle specific ring finger proteins as potential regulators of the titin kinase domain,” Journal of Molecular Biology, vol. 306, no. 4, pp. 717–726, 2001.
- S. C. Kandarian and E. J. Stevenson, “Molecular events in skeletal muscle during disuse atrophy,” Exercise and Sport Sciences Reviews, vol. 30, no. 3, pp. 111–116, 2002.
- B. S. Shenkman, T. L. Nemirovskaya, I. N. Belozerova et al., “Effects of Ca2+-binding agent on unloaded rat soleus: muscle morphology and sarcomeric titin content,” European Space Agency, no. 501, pp. 107–108, 2002.
- B. S. Shenkman, K. S. Litvinova, T. L. Nemirovskaya, Z. A. Podlubnaya, I. M. Vikhlyantsev, and I. B. Kozlovskaya, “Afferent and peripheral control of muscle fiber properties during gravitational unloading,” Journal of Gravitational Physiology, vol. 11, no. 2, pp. P111–P114, 2004.
- K. Goto, R. Okuyama, M. Honda et al., “Profiles of connectin (titin) in atrophied soleus muscle induced by unloading of rats,” Journal of Applied Physiology, vol. 94, no. 3, pp. 897–902, 2003.
- H. Chang, L. Zhang, P.-T. Xu et al., “Nuclear translocation of calpain-2 regulates propensity toward apoptosis in cardiomyocytes of tail-suspended rats,” Journal of Cellular Biochemistry, vol. 112, no. 2, pp. 571–580, 2011.
- P. O. Hasselgren and J. E. Fischer, “Counter-regulatory hormones and mechanisms in amino acid metabolism with special reference to the catabolic response in skeletal muscle,” Current Opinion in Clinical Nutrition and Metabolic Care, vol. 2, no. 1, pp. 9–14, 1999.
- R. T. Jagoe and A. L. Goldberg, “What do we really know about the ubiquitin-proteasome pathway in muscle atrophy?” Current Opinion in Clinical Nutrition and Metabolic Care, vol. 4, no. 3, pp. 183–190, 2001.
- S. H. Lecker, R. T. Jagoe, A. Gilbert et al., “Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression,” The FASEB Journal, vol. 18, no. 1, pp. 39–51, 2004.
- M. D. Gomes, S. H. Lecker, R. T. Jagoe, A. Navon, and A. L. Goldberg, “Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 25, pp. 14440–14445, 2001.
- R. Medina, S. S. Wing, A. Haas, and A. L. Goldberg, “Activation of the ubiquitin-ATP-dependent proteolytic system in skeletal muscle during fasting and denervation atrophy,” Biomedica Biochimica Acta, vol. 50, no. 4–6, pp. 347–356, 1991.
- A. S. McElhinny, C. N. Perry, C. C. Witt, S. Labeit, and C. C. Gregorio, “Muscle-specific RING finger-2 (MURF-2) is important for microtubule, intermediate filament and sarcomeric M-line maintenance in striated muscle development,” Journal of Cell Science, vol. 117, no. 15, pp. 3175–3188, 2004.
- C. C. Gregorio, C. N. Perry, and A. S. Mcelhinny, “Functional properties of the titin/connectin-associated proteins, the muscle-specific RING finger proteins (MURFs), in striated muscle,” Journal of Muscle Research and Cell Motility, vol. 26, no. 6–8, pp. 389–400, 2005.
- S. W. Jones, R. J. Hill, P. A. Krasney, B. O'Conner, N. Peirce, and P. L. Greenhaff, “Disuse atrophy and exercise rehabilitation in humans profoundly affects the expression of genes associated with the regulation of skeletal muscle mass,” The FASEB Journal, vol. 18, no. 9, pp. 1025–1027, 2004.
- L. A. Tintignac, J. Lagirand, S. Batonnet, V. Sirri, M. P. Leibovitch, and S. A. Leibovitch, “Degradation of MyoD mediated by the SCF (MAFbx) ubiquitin ligase,” The Journal of Biological Chemistry, vol. 280, no. 4, pp. 2847–2856, 2005.
- J. Lagirand-Cantaloube, N. Offner, A. Csibi et al., “The initiation factor eIF3-f is a major target for Atrogin1/MAFbx function in skeletal muscle atrophy,” The EMBO Journal, vol. 27, no. 8, pp. 1266–1276, 2008.
- V. Kedar, H. McDonough, R. Arya, H. H. Li, H. A. Rockman, and C. Patterson, “Muscle-specific RING finger 1 is a bona fide ubiquitin ligase that degrades cardiac troponin I,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 52, pp. 18135–18140, 2004.
- B. A. Clarke, D. Drujan, M. S. Willis et al., “The E3 Ligase MuRF1 degrades myosin heavy chain protein in dexamethasone-treated skeletal muscle,” Cell Metabolism, vol. 6, no. 5, pp. 376–385, 2007.
- D. L. Allen, E. R. Bandstra, B. C. Harrison et al., “Effects of spaceflight on murine skeletal muscle gene expression,” Journal of Applied Physiology, vol. 106, no. 2, pp. 582–592, 2009.
- S. M. Phillips, E. I. Glover, and M. J. Rennie, “Alterations of protein turnover underlying disuse atrophy in human skeletal muscle,” Journal of Applied Physiology, vol. 107, no. 3, pp. 645–654, 2009.
- M. Salanova, G. Schiffl, B. Püttmann, B. G. Schoser, and D. Blottner, “Molecular biomarkers monitoring human skeletal muscle fibres and microvasculature following long-term bed rest with and without countermeasures,” Journal of Anatomy, vol. 212, no. 3, pp. 306–318, 2008.
- T. Ogawa, H. Furochi, M. Mameoka et al., “Ubiquitin ligase gene expression in healthy volunteers with 20-day bedrest,” Muscle and Nerve, vol. 34, no. 4, pp. 463–469, 2006.
- K. A. Reich, Y. W. Chen, P. D. Thompson, E. P. Hoffman, and P. M. Clarkson, “Forty-eight hours of unloading and 24 h of reloading lead to changes in global gene expression patterns related to ubiquitination and oxidative stress in humans,” Journal of Applied Physiology, vol. 109, no. 5, pp. 1404–1415, 2010.
- P. A. Tesch, F. von Walden, T. Gustafsson, R. M. Linnehan, and T. A. Trappe, “Skeletal muscle proteolysis in response to short-term unloading in humans,” Journal of Applied Physiology, vol. 105, no. 3, pp. 902–906, 2008.
- M. D. de Boer, A. Selby, P. Atherton et al., “The temporal responses of protein synthesis, gene expression and cell signalling in human quadriceps muscle and patellar tendon to disuse,” The Journal of Physiology, vol. 585, no. 1, pp. 241–251, 2007.
- E. V. Kachaeva, O. V. Turtikova, T. A. Leĭnsoo, and B. S. Shenkman, “Insulin-like growth factor 1 and the key markers of proteolysis during the acute period of readaptation of the muscle atrophied as a result of unloading,” Biofizika, vol. 55, no. 6, pp. 1108–1116, 2010.
- M. Vermaelen, J.-F. Marini, A. Chopard, Y. Benyamin, J. Mercier, and C. Astier, “Ubiquitin targeting of rat muscle proteins during short periods of unloading,” Acta Physiologica Scandinavica, vol. 185, no. 1, pp. 33–40, 2005.
- L. Tskhovrebova and J. Trinick, “Muscle disease: a giant feels the strain,” Nature Medicine, vol. 11, no. 5, pp. 478–479, 2005.
- S. Schiaffino and HanzlíkováVěra, “Studies on the effect of denervation in developing muscle. II. The lysosomal system,” Journal of Ultrasructure Research, vol. 39, no. 1-2, pp. 1–14, 1972.
- S. H. Witt, H. Granzier, C. C. Witt, and S. Labeit, “MURF-1 and MURF-2 target a specific subset of myofibrillar proteins redundantly: towards understanding MURF-dependent muscle ubiquitination,” Journal of Molecular Biology, vol. 350, no. 4, pp. 713–722, 2005.
- A. S. Moriscot, I. L. Baptista, J. Bogomolovas et al., “MuRF1 is a muscle fiber-type II associated factor and together with MuRF2 regulates type-II fiber trophicity and maintenance,” Journal of Structural Biology, vol. 170, no. 2, pp. 344–353, 2010.
- S. Labeit, C. H. Kohl, C. C. Witt, D. Labeit, J. Jung, and H. Granzier, “Modulation of muscle atrophy, fatigue and MLC phosphorylation by MuRF1 as indicated by hindlimb suspension studies on MuRF1-KO mice,” Journal of Biomedicine and Biotechnology, vol. 2010, Article ID 693741, 9 pages, 2010.
- C. Bozzo, L. Stevens, L. Toniolo, Y. Mounier, and C. Reggiani, “Increased phosphorylation of myosin light chain associated with slow-to-fast transition in rat soleus,” American Journal of Physiology, vol. 285, no. 3, pp. C575–C583, 2003.
- M. J. Potthoff, H. Wu, M. A. Arnold et al., “Histone deacetylase degradation and MEF2 activation promote the formation of slow-twitch myofibers,” The Journal of Clinical Investigation, vol. 117, no. 9, pp. 2459–2467, 2007.
- U. Späte and P. C. Schulze, “Proinflammatory cytokines and skeletal muscle,” Current Opinion in Clinical Nutrition and Metabolic Care, vol. 7, no. 3, pp. 265–269, 2004.
- I. W. McKinnell and M. A. Rudnicki, “Molecular mechanisms of muscle atrophy,” Cell, vol. 119, no. 7, pp. 907–910, 2004.
- D. Cai, J. D. Frantz, N. E. Tawa et al., “IKKβ/NF-κB activation causes severe muscle wasting in mice,” Cell, vol. 119, no. 2, pp. 285–298, 2004.
- R. Bridge Hunter, E. J. Stevenson, C. Alan Koncarevi, H. Mitchell-Felton, D. A. Essig, and S. C. Kandarian, “Activation of an alternative NF-κB pathway in skeletal muscle during disuse atrophy,” The FASEB Journal, vol. 16, no. 6, pp. 529–538, 2002.
- A. R. Judge, A. Koncarevic, R. B. Hunter, H. C. Liou, R. W. Jackman, and S. C. Kandarian, “Role for IκBα, but not c-Rel, in skeletal muscle atrophy,” American Journal of Physiology, vol. 292, no. 1, pp. C372–C382, 2007.
- S. M. Senf, S. L. Dodd, J. M. McClung, and A. R. Judge, “Hsp70 overexpression inhibits NF-κB and Foxo3a transcriptional activities and prevents skeletal muscle atrophy,” The FASEB Journal, vol. 22, no. 11, pp. 3836–3845, 2008.
- T. N. Stitt, D. Drujan, B. A. Clarke et al., “The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors,” Molecular Cell, vol. 14, no. 3, pp. 395–403, 2004.
- K. H. Kaestner, W. Knöchel, and D. E. Martínez, “Unified nomenclature for the winged helix/forkhead transcription factors,” Genes and Development, vol. 14, no. 2, pp. 142–146, 2000.
- H. Huang and D. J. Tindall, “Regulation of FOXO protein stability via ubiquitination and proteasome degradation,” Biochimica et Biophysica Acta, vol. 1813, no. 11, pp. 1961–1964, 2011.
- M. Sandri, C. Sandri, A. Gilbert et al., “Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy,” Cell, vol. 117, no. 3, pp. 399–412, 2004.
- Y. Kamei, S. Miura, M. Suzuki et al., “Skeletal muscle FOXO1 (FKHR) transgenic mice have less skeletal muscle mass, down-regulated type I (slow twitch/red muscle) fiber genes, and impaired glycemic control,” The Journal of Biological Chemistry, vol. 279, no. 39, pp. 41114–41123, 2004.
- C. De Alvaro, T. Teruel, R. Hernandez, and M. Lorenzo, “Tumor necrosis factor alpha produces insulin resistance in skeletal muscle by activation of inhibitor kappaB kinase in a p38 MAPK-dependent manner,” The Journal of Biological Chemistry, vol. 279, no. 17, pp. 17070–17078, 2004.
- C. Dogra, H. Changotra, N. Wedhas, X. Qin, J. E. Wergedal, and A. Kumar, “TNF-related weak inducer of apoptosis (TWEAK) is a potent skeletal muscle-wasting cytokine,” The FASEB Journal, vol. 21, no. 8, pp. 1857–1869, 2007.
- J. Hirosumi, G. Tuncman, L. Chang et al., “A central, role for JNK in obesity and insulin resistance,” Nature, vol. 420, no. 6913, pp. 333–336, 2002.
- F. Mourkioti, P. Kratsios, T. Luedde et al., “Targeted ablation of IKK2 improves skeletal muscle strength, maintains mass, and promotes regeneration,” The Journal of Clinical Investigation, vol. 116, no. 11, pp. 2945–2954, 2006.
- B. Han, M. J. Zhu, C. Ma, and M. Du, “Rat hindlimb unloading down-regulates insulin like growth factor-1 signaling and AMP-activated protein kinase, and leads to severe atrophy of the soleus muscle,” Applied Physiology, Nutrition and Metabolism, vol. 32, no. 6, pp. 1115–1123, 2007.
- R. Nakao, K. Hirasaka, J. Goto et al., “Ubiquitin ligase Cbl-b is a negative regulator for insulin-like growth factor 1 signaling during muscle atrophy caused by unloading,” Molecular and Cellular Biology, vol. 29, no. 17, pp. 4798–4811, 2009.
- C. McFarlane, A. Hennebry, M. Thomas et al., “Myostatin signals through Pax7 to regulate satellite cell self-renewal,” Experimental Cell Research, vol. 314, no. 2, pp. 317–329, 2008.
- D. L. Allen and T. G. Unterman, “Regulation of myostatin expression and myoblast differentiation by FoxO and SMAD transcription factors,” American Journal of Physiology, vol. 292, no. 1, pp. C188–C199, 2007.
- S. McCroskery, M. Thomas, L. Maxwell, M. Sharma, and R. Kambadur, “Myostatin negatively regulates satellite cell activation and self-renewal,” Journal of Cell Biology, vol. 162, no. 6, pp. 1135–1147, 2003.
- J. Massagué, J. Seoane, and D. Wotton, “Smad transcription factors,” Genes and Development, vol. 19, no. 23, pp. 2783–2810, 2005.
- R. R. Gomis, C. Alarcón, W. He et al., “A FoxO-Smad synexpression group in human keratinocytes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 34, pp. 12747–12752, 2006.
- T. Shintani and D. J. Klionsky, “Autophagy in health and disease: a double-edged sword,” Science, vol. 306, no. 5698, pp. 990–995, 2004.
- M. F. N. O'Leary and D. A. Hood, “Denervation-induced oxidative stress and autophagy signaling in muscle,” Autophagy, vol. 5, no. 2, pp. 230–231, 2009.
- M. E. Tischler, S. Rosenberg, S. Satarug et al., “Different mechanisms of increased proteolysis in atrophy induced by denervation or unweighting of rat soleus muscle,” Metabolism, vol. 39, no. 7, pp. 756–763, 1990.
- K. Furuno, M. N. Goodman, and A. L. Goldberg, “Role of different proteolytic systems in the degradation of muscle proteins during denervation atrophy,” The Journal of Biological Chemistry, vol. 265, no. 15, pp. 8550–8557, 1990.
- C. Deval, S. Mordier, C. Obled et al., “Identification of cathepsin L as a differentially expressed message associated with skeletal muscle wasting,” Biochemical Journal, vol. 360, no. 1, pp. 143–150, 2001.
- M. Sandri, “Signaling in muscle atrophy and hypertrophy,” Physiology, vol. 23, no. 3, pp. 160–170, 2008.
- D. E. Goll, G. Neti, S. W. Mares, and V. F. Thompson, “Myofibrillar protein turnover: the proteasome and the calpains,” Journal of Animal Science, vol. 86, no. 14, pp. E19–E35, 2008.
- A. Tassa, M. P. Roux, D. Attaix, and D. M. Bechet, “Class III phosphoinositide 3-kinase-Beclin1 complex mediates the amino acid-dependent regulation of autophagy in C2C2 myotubes,” Biochemical Journal, vol. 376, no. 3, pp. 577–586, 2003.
- C. Mammucari, G. Milan, V. Romanello et al., “FoxO3 controls autophagy in skeletal muscle in vivo,” Cell Metabolism, vol. 6, no. 6, pp. 458–471, 2007.
- J. Zhao, J. J. Brault, A. Schild et al., “FoxO3 coordinately activates protein degradation by the autophagic/lysosomal and proteasomal pathways in atrophying muscle cells,” Cell Metabolism, vol. 6, no. 6, pp. 472–483, 2007.
- J. Du, X. Wang, C. Miereles et al., “Activation of caspase-3 is an initial step triggering accelerated muscle proteolysis in catabolic conditions,” The Journal of Clinical Investigation, vol. 113, no. 1, pp. 115–123, 2004.
- P. Berthon, S. Duguez, F. B. Favier et al., “Regulation of ubiquitin-proteasome system, caspase enzyme activities, and extracellular proteinases in rat soleus muscle in response to unloading,” Pflugers Archiv European Journal of Physiology, vol. 454, no. 4, pp. 625–633, 2007.
- E. Vazeille, A. Codran, A. Claustre et al., “The ubiquitin-proteasome and the mitochondria-associated apoptotic pathways are sequentially downregulated during recovery after immobilization-induced muscle atrophy,” American Journal of Physiology, vol. 295, no. 5, pp. E1181–E1190, 2008.
- P. M. Siu, E. E. Pistilli, and S. E. Alway, “Apoptotic responses to hindlimb suspension in gastrocnemius muscles from young adult and aged rats,” American Journal of Physiology, vol. 289, no. 4, pp. R1015–R1026, 2005.
- C. Leeuwenburgh, C. M. Gurley, B. A. Strotman, and E. E. Dupont-Versteegden, “Age-related differences in apoptosis with disuse atrophy in soleus muscle,” American Journal of Physiology, vol. 288, no. 5, pp. R1288–R1296, 2005.
- M. Ohanna, A. K. Sobering, T. Lapointe et al., “Atrophy of S6K1-/- skeletal muscle cells reveals distinct mTOR effectors for cell cycle and size control,” Nature Cell Biology, vol. 7, no. 3, pp. 286–294, 2005.
- E. J. Henriksen, M. E. Tischler, and D. G. Johnson, “Increased response to insulin of glucose metabolism in the 6-day unloaded rat soleus muscle,” The Journal of Biological Chemistry, vol. 261, no. 23, pp. 10707–10712, 1986.
- S. C. Bodine, E. Latres, S. Baumhueter et al., “Identification of ubiquitin ligases required for skeletal Muscle Atrophy,” Science, vol. 294, no. 5547, pp. 1704–1708, 2001.
- W. H. Shen, D. W. Boyle, P. Wisniowski, A. Bade, and E. A. Liechty, “Insulin and IGF-I stimulate the formation of the eukaryotic initiation factor 4F complex and protein synthesis in C2C12 myotubes independent of availability of external amino acids,” Journal of Endocrinology, vol. 185, no. 2, pp. 275–289, 2005.
- T. L. Hilder, J. C. L. Tou, R. E. Grindeland, C. E. Wade, and L. M. Graves, “Phosphorylation of insulin receptor substrate-1 serine 307 correlates with JNK activity in atrophic skeletal muscle,” FEBS Letters, vol. 553, no. 1-2, pp. 63–67, 2003.
- S. Machida and F. W. Booth, “Changes in signalling molecule levels in 10-day hindlimb immobilized rat muscles,” Acta Physiologica Scandinavica, vol. 183, no. 2, pp. 171–179, 2005.
- K. Csukly, T. Marqueste, and P. Gardiner, “Sensitivity of rat soleus muscle to a mechanical stimulus is decreased following hindlimb unweighting,” European Journal of Applied Physiology, vol. 95, no. 2-3, pp. 243–249, 2005.
- P. K. Paul, S. K. Gupta, S. Bhatnagar et al., “Targeted ablation of TRAF6 inhibits skeletal muscle wasting in mice,” Journal of Cell Biology, vol. 191, no. 7, pp. 1395–1411, 2010.
- A. Csibi, L. A. Tintignac, M. P. Leibovitch, and S. A. Leibovitch, “eIF3-f function in skeletal muscles: to stand at the crossroads of atrophy and hypertrophy,” Cell Cycle, vol. 7, no. 12, pp. 1698–1701, 2008.
- C. Zhou, F. Arslan, S. Wee et al., “PCI proteins eIF3e and eIF3m define distinct translation initiation factor 3 complexes,” BMC Biology, vol. 3, article 14, 2005.
- A. L. Serrano, B. Baeza-Raja, E. Perdiguero, M. Jardí, and P. Muñoz-Cánoves, “Interleukin-6 is an essential regulator of satellite cell-mediated skeletal muscle hypertrophy,” Cell Metabolism, vol. 7, no. 1, pp. 33–44, 2008.
- P. Loughna, G. Goldspink, and D. F. Goldspink, “Effect of inactivity and passive stretch on protein turnover in phasic and postural rat muscles,” Journal of Applied Physiology, vol. 61, no. 1, pp. 173–179, 1986.
- K. Ojima, Y. Kawabata, H. Nakao et al., “Dynamic distribution of muscle-specific calpain in mice has a key role in physical-stress adaptation and is impaired in muscular dystrophy,” The Journal of Clinical Investigation, vol. 120, no. 8, pp. 2672–2683, 2010.
- I. L. Baptista, M. L. Leal, G. G. Artioli et al., “Leucine attenuates skeletal muscle wasting via inhibition of ubiquitin ligases,” Muscle and Nerve, vol. 41, no. 6, pp. 800–808, 2010.