While mechanotransductive signal is proven essential for tissue regeneration, it is critical to determine specific cellular responses to such mechanical signals and the underlying mechanism. Dynamic fluid flow induced by mechanical loading has been shown to have the potential to regulate bone adaptation and mitigate bone loss. Mechanotransduction pathways are of great interests in elucidating how mechanical signals produce such observed effects, including reduced bone loss, increased bone formation, and osteogenic cell differentiation. The objective of this review is to develop a molecular understanding of the mechanotransduction processes in tissue regeneration, which may provide new insights into bone physiology. We discussed the potential for mechanical loading to induce dynamic bone fluid flow, regulation of bone adaptation, and optimization of stimulation parameters in various loading regimens. The potential for mechanical loading to regulate microcirculation is also discussed. Particularly, attention is allotted to the potential cellular and molecular pathways in response to loading, including osteocytes associated with Wnt signaling, elevation of marrow stem cells, and suppression of adipotic cells, as well as the roles of LRP5 and microRNA. These data and discussions highlight the complex yet highly coordinated process of mechanotransduction in bone tissue regeneration.

1. Introduction

High physical activity level has been associated with high bone mass and low fracture risk and is therefore recommended to reduce fractures [13]. The ability of musculoskeletal tissue to respond to changes in its functional milieu is one of the most intriguing aspects of such living tissue and certainly contributes to its success as a structure. Bone and muscle rapidly accommodate changes in their functional environment to ensure that sufficient skeletal mass is appropriately placed to withstand the regions of functional activity, an attribute described as Wolff’s Law [4, 5]. This adaptive capability of musculoskeletal tissues suggests that biophysical stimuli may be able to provide a site-specific, exogenous treatment to control both bone mass and morphology. The premise of mechanical influence on bone morphology has become a basic tenet of bone physiology [68]. Absence of functional loading results in loss of bone mass [912], while exercise or increased activity results in increased bone mass [1315]. Similarly, increasing exercise of musculoskeletal tissue can significantly increase blood flow, oxygen, and the exchange of fluid in muscle. During muscle contraction, several mechanisms regulate blood flow to ensure a close coupling between muscle oxygen delivery and metabolic demand [1621]. Based on the muscle pump theory, vascular arteries and veins within skeletal muscles are compressed upon muscle contraction, therefore increasing the arteriovenous pressure gradient and promoting capillary filtration [2224]. To define the formal relationship between mechanical milieu and the adaptive response, the relationship between muscle pump and interstitial fluid flow will prove instrumental in devising a mechanical intervention for musculoskeletal disorders such as osteoporosis, muscle fatigue, and atrophy, designing biomechanical means to accelerate fracture healing, and promoting bony ingrowth.

To adapt to the changing demands of mechanics, bone mass and bone morphology can be regulated via bone remodeling at specific sites. This crucial process of structural remodeling of the bone involves bone resorption and the subsequent bone formation. However, difficulties to determine specific mechanical components will hamper our understanding of bone remodeling related diseases, as well as limiting our judgments on bone fractures and healing capacity. Therefore, continuous studies of the bone remodeling process, for example, to determine the mechanical model of this remodeling process, can ultimately benefit the intervention on prevention and treatment of musculoskeletal disorders.

1.1. Bone Adaptation to Mechanical Loading

In the past few decades, researchers have suggested that the strain and stress are the main regulation parameters of bone cell response to mechanical signals. For instance, some researchers have proposed “invariant” parameter whose strength does not depend on a reference system, which is similar to “strain energy density” [25, 26] that is capable of modulating bone cell response to mechanical signals. This theory is consistent with the idea of bone self-regulation [27, 28]. There are many theories regarding bone self-regulation, including the degree of strain regulation on bone modeling process, time-dependent bone modeling, and remodeling processes [27]. A regulatory model with a variety of influential factors, including the magnitude of strain/stress, number of loading cycles, number of loading occurrences, tensor of strain, and the strain energy density, can result in bone self-regulation. It is still difficult to distinguish the independent effects of these factors and to determine the specific factors that regulate bone remodeling. To explore these mechanical hypotheses, it must be determined whether bone cells are directly or indirectly regulated by these mechanical parameters. By far, there is little evidence in the relationship between the maximal strain, stress, and bone morphology [9]. Specific mechanical parameters to initiate or discontinue mechanical response of bone cells remain to be further determined.

1.2. The Role of Dynamic and Temporal Mechanical Signals

A recent discovery mainly uses the temporal portion of the stimulus signal, such as the number of strain cycles, loading frequency, and strain gradient, to explain the mechanism of bone response to mechanical stimuli at the cellular level. Under stimuli with the same strain magnitude, higher strain cycle will cause a more significant adaptive response [29, 30]. Similarly, signals at 15 to 60 Hz, in comparison to signals at about 1 Hz, can stimulate more bone growth [31, 32] (Figure 1). Maintenance of the existing bone mass requires different frequencies (1 to 60 Hz) of stimuli with continuous sinusoidal signal (10 minutes/day) to achieve different loading magnitude “threshold value.” Experiments have shown that stimulation at 1 Hz requires 700 με of longitudinal strain to maintain the existing cortical bone mass, while stimulation at 30 Hz only requires 400 με. If 60 Hz of the stimulation signal is used, only 270 με of strain signal is sufficient to maintain the amount of cortical bone. A strong link has been found between this frequency-sensitive cortical bone remodeling process and the magnitude of bone fluid flow, in which the flow is directly regulated by the frequency () [33]. Turner et al. have found that increased loading rate with a constant loading strain on the adult rat tibia can significantly improve bone formation [34]. Meanwhile, the amount of new bone formation is directly proportional to the strain loading rate. If we associate the external mechanical loading parameters with bone remodeling, then we will most likely be able to predict the periosteal new bone formation based on the strain gradient [9, 35, 36]. Many in vivo and in vitro experimental evidences have pointed out that bone adapts to dynamic mechanical loads rather than a static load [34, 37, 38]. All these show that dynamic and temporal mechanical signals, along with the potential load-induced fluid dynamics, are necessary for promoting the bone adaptation.

1.3. Mechanotransduction and Interstitial Bone Fluid Flow

Tensile strain is closely related to interstitial bone fluid flow caused by bone matrix deformation. Mechanical loading can cause variations of bone matrix deformation and interstitial fluid pathways within bone, thereby generating hydraulic pressure gradient within the capillary bed, leading to interstitial bone fluid flow [39]. Fluid flow-induced shear stress within bone has been considered as the source of how bone cells sense mechanical stimulation [4044]. Bone interstitial fluid is filling a variety of voids and channels within the bone matrix, including lacunae-canaliculi, bone tubules, Haversian canal and Volkmann canal, and osteon [45]. Mechanical loading-induced interstitial bone fluid flow may play a role in mechanical sensing, bone cells response, signal transmission, transfer of nutrients, and so forth. This interstitial fluid flow within cortical bone is thought to be a critical regulator for bone mass and morphology [4648]. We believe that this is a key mechanism of how bone, at certain loading frequency, strain, strain cycle, and strain gradient, leads to load-induced bone modeling, remodeling, and maintenance.

1.4. The Use of Noninvasive Dynamic Flow Stimulation to Prevent Bone Loss

Experiments on dogs during development have shown that increased venous pressure can promote new bone formation in the periosteum [49]. The data indicated that increased venous pressure will increase blood supply from the capillaries to the bone tissue, which may lead to new bone formation in the periosteum. In a rat tail suspension experiment, suturing tibial vein increased tibial marrow cavity pressure (ImP) (27.8 mmHg versus 16.4 mmHg, ) in the experimental group compared to the control, which suggested that the pore fluid flow pressure reinforced by the suture is inversely proportional to the bone cross section. In the experimental group of vein suture, bone mineral content and trabecular bone density were significantly higher within 19 days [50]. These results indicated that bone fluid flow may not solely rely on the mechanical loads to cause bone adaptive response. Moreover, intravenous fluid pressure is directly related to hydraulic ImP, which implies that the adaptive response can be altered by intravenous bone muscle pump hydraulic effect that prevents bone loss noninvasively.

1.5. Marrow Pressure and Bone Strain Generated by Mechanical Loading

Recent studies have revealed that induced marrow fluid pressure and bone strain by mechanical stimulation were dependent on dynamic loading parameters and optimized at certain loading frequencies [33]. A previous study has evaluated oscillatory electrical muscle stimulation- (MS-) induced ImP and bone strain as function of stimulation frequency. MS generated femoral ImP and bone strain were measured with frequencies of 1–100 Hz in rats. A maximum ImP of  mmHg at 20 Hz and a maximum matrix strain of με at 10 Hz were generated by oscillatory MS. These results suggest that muscle force alone, if applied at a low rate, such as resistant weight lifting with high intensity, would not be able to generate sufficient strain and fluid pressure in bone. MS with a relatively high rate and a small magnitude, however, can trigger significant fluid pressure in the skeleton. To identify induced ImP dynamics and bone strain factors in vivo using a noninvasive method, a more recent study used dynamic hydraulic stimulation (DHS) and evaluated its immediate effects on local and distant ImP and bone strain in response to a range of loading frequencies of 1 Hz to 10 Hz [5154]. DHS-induced ImP in the stimulated tibia was in a nonlinear fashion over the range of loading frequencies, where they peaked at 2 Hz with a maximum ImP of  mmHg. Maximal bone strain was less than 8 με, measured at all loading frequencies. No detectable induction of ImP or bone strain was observed in the distant site away from the stimulation. Oscillatory DHS may regulate local fluid dynamics with minimal mechanical matrix strain, which is highly frequency dependent.

1.6. Mechanical Loading-Induced Bone Loss Attenuation and Fracture Healing

An in vivo study used a rat functional disuse model to evaluate the mitigation potential of MS in disused trabecular bone and investigated the importance of the optimized stimulation frequency (1, 20, 50, and 100 Hz) in the loading regimen [52]. Analyzed by microCT and histomorphometry, MS for 10 min/day with a total of 4 weeks showed improvements in metaphyseal trabecular bone quantity and structure at midfrequency (20 Hz and 50 Hz), in which 50 Hz of stimulation demonstrated the greatest preventive effect on the skeleton against functional disuse (up to +147% in bone volume fraction, +38% in trabecular number, and −36% in trabecular separation compared to HLS control). These data imply that MS, applied at a high frequency with a low magnitude for a short duration, is able to mitigate bone loss induced by the functional disuse (Figure 2). In addition, another study used DHS that elevates in vivo oscillatory BFF via ImP, to evaluate the effects of DHS on mitigation of trabecular bone loss and structural alteration in a rat disuse model [5356]. DHS of 2 Hz for 20 min/day, 5 days/week, and a total of 4-week experiment improved the bone quantity and microarchitecture (+83% in bone volume fraction, +25% in trabecular number, and −26% in trabecular separation compared to HLS control). The data demonstrate DHS’s potentials to mitigate bone loss induced by functional disuse (Figure 3).

Taking into account that MS can increase blood flow and ImP in the muscle and marrow cavity [33, 57] and that blood flow has a close relationship with fracture healing, it is likely that applying MS may result in an enhancement of fracture healing. Using a rabbit model with a 3 mm tibial transverse osteotomy, Park and Silva have shown that fracture treated with MS showed 31% higher mineral content and 27% larger callus area than control osteotomies at eight weeks. In addition, the maximum torque, torsional stiffness, angular displacement at maximum torque, and energy required for failure of specimens in the study group were 62%, 29%, 34.6%, and 124% higher, respectively, compared to the control at eight weeks [58]. The results suggested that the use of MS can enhance callus mineralization and biomechanical strength in the callus region. This may, at least partially, be the result of MS enhanced blood circulation. Using a bone chamber, Winet and his group observed that muscle contractions directly increased bone blood flow rates by 130% but uncoupled from mechanical loading, while heart rates and blood pressure did not significantly increase due to the MS treatment [59]. Thus, enhanced fluid flow by MS may directly involve increasing fluid flow in callus and trigger anabolic response under such acute conditions, for example, fracture healing.

2. Potential Cellular and Molecular Pathways of Mechanotransduction

Bone remodeling involves all related cell types, that is, osteoblast, osteoclast, osteocyte, T-cells, B-cells, megakaryocyte, and lining cells. Thus, all these cells are potentially mechanosensitive and even interrelated. These cells respond to mechanical loading with expression of specific molecular pathways. This section will discuss several potential pathways involved in mechanical stimulation induced adaptation.

2.1. Basic Multicellular Units (BMU)

To explore the interrelation among overall bone cells, a cluster of bone forming and bone resorption cells among dynamic and temporal adaptation structures are known as “basic multicellular units” (BMUs) [60, 61]. Bone adaptation occurs constantly and each cycle may take over several weeks. Such processes are performed with combination of resorption and formation. Each phase can involve targeted molecular and gene activations. An active BMU consists of a leading front of bone-resorbing osteoclasts. Reversal cells, of unclear phenotype, follow the osteoclasts, covering the newly exposed bone surface, and prepare them for deposition of replacement bone, following a deposition of an unmineralized bone matrix known as osteoid. Related molecular and genetic factors are represented in this temporal sequence (Figure 4).

In response to mechanical loading, the first stage of remodeling reflects the detection of initiating triggering signals such as fluid flow and/or any other physical stimulation, for example, pressure, electrical, and acoustic waves. Prior to activation, the resting bone surface is covered with bone-lining cells, including preosteoblasts intercalated with osteomacs. B-cells are present in the bone marrow and secrete osteoprotegerin (OPG) that suppresses osteoclastogenesis. During the activation phase, the endocrine bone remodeling signal parathyroid hormone (PTH) binds to the PTH receptor on preosteoblasts. Damage to the mineralized bone matrix results in localized osteocyte apoptosis, reducing the local transforming growth factor β (TGF-β) concentration and its inhibition of osteoclastogenesis. In the resorption phase, in response to PTH signaling, MCP-1 is released from osteoblasts and recruits preosteoclasts to the bone surface. Additionally, osteoblastic expression of OPG is decreased, and production of CSF-1 and RANKL is increased to promote proliferation of osteoclast precursors and differentiation of mature osteoclasts. Mature osteoclasts anchor to RGD-binding sites, creating a localized microenvironment (sealed zone) that facilitates degradation of the mineralized bone matrix. In the reversal phase, reversal cells engulf and remove demineralized undigested collagen from the bone surface. Transition signals are generated that halt bone resorption and stimulate the bone formation process. During the formation phase, formation signals and molecules arise from the degraded bone matrix, mature osteoclasts, and potentially reversal cells. PTH and mechanical activation of osteocytes reduce sclerostin expression, allowing for Wnt-directed bone formation to occur. Finally, in the termination phase, sclerostin expression likely returns, and bone formation ceases. The newly deposited osteoid is mineralized; the bone surfaces return to a resting state with bone-lining cells intercalated with osteomacs, and the remodeling cycle ends. Mechanical stimulation is likely involved in each of these phases and eventually regulates related molecular and genetic factors. This unique spatial and temporal arrangement of cells within the BMU is critical to bone remodeling, ensuring coordination of the distinct and sequential phases of this process: activation, resorption, reversal, formation, and termination.

2.2. Osteocyte and Its Response to Mechanical Signals Coupled with Wnt Signaling

Osteocytes, cells embedded within the mineralized matrix of bone, are becoming the target of intensive investigation [6164]. Osteoblasts are defined as cells that make bone matrix and are thought to translate mechanical loading into biochemical signals that affect bone modeling and remodeling. The interrelationship between osteoblasts and osteocytes would be expected to have the same lineage, yet these cells also have distinct differences, particularly in their responses to mechanical loading and utilization of the various biochemical pathways to accomplish their respective functions. Among many factors, Wnt/β-catenin signaling pathway may be recognized as an important regulator of bone mass and bone cell functions [61, 64]. While osteocytes are embedded within the mineral matrix, Wnt/β-catenin signaling pathway may serve as a transmitter to transfer mechanical signals sensed by osteocytes to the surface of bone. Further, new data suggest that the Wnt/β-catenin pathway in osteocytes may be triggered by crosstalk with the prostaglandin pathway in response to loading which then leads to a decrease in expression of negative regulators of the pathway such as sclerostin (Sost) and Dickkopf-related protein 1 (Dkk-1) [64, 65]. Figure 5 indicates potential pathway in response to mechanical loading.

It has been shown that the Wnt pathway is closely involved in bone cell differentiation, proliferation, and apoptosis [64, 66]. Regulation of the Wnt/β-catenin signaling pathway is vested largely in proteins that either act as competitive binders of Wnts, notably the secreted frizzled-related proteins (sFRP) family, or act at the level of low-density lipoprotein receptor-related protein 5 (LRP5), including the osteocyte specific protein, sclerostin (the Sost gene product), and the Dkk proteins, particularly Dkk-1 and Dkk-2 [64, 6669]. Sclerostin has been shown to be made by mature osteocytes and inhibits Wnt/β-catenin signaling by binding to LRP5 and preventing the binding of Wnt. Dkk-1 is highly expressed in osteocytes [6769]. Clinical trial studies using antibodies to sclerostin have also been shown to result in increased bone mass, suggesting that targeting of these negative regulators of Wnt/β-catenin signaling pathway might be anabolic treatments for diseases such as osteoporosis [67]. Finally, mechanical loading has been shown to reduce sclerostin levels in bone [67], suggesting that one of the targets of the pathways, activated by the early events after mechanical loading, is the genes encoding these negative modulators of the Wnt/β-catenin signaling pathway.

2.3. Mechanical Signal Triggered Bone Marrow Cells Alteration

The data from disuse osteopenia and clinical osteoporosis have shown significant reduction of bone density and structural integrity, culminating in an elevated risk of skeletal fracture. Concurrently, a marked reduction in the available bone-marrow-derived population of mesenchymal stem cells (MSCs) [70] jeopardizes the regenerative potential that is critical to the recovery from bone loss, musculoskeletal injury, and diseases. A potential way to combat the deterioration involves harnessing the sensitivity of bone to mechanical signals, which is crucial in defining, maintaining, and recovering bone mass. As discussed above, bone cells, that is, osteoblast, osteoclast, and osteocyte, may sense external mechanical loading directly and perform balance of formation and resorption in the remodeling process; specific mechanotransductive signals may also bias MSC differentiation towards osteoblastogenesis and away from adipogenesis. Mechanical targeting of the bone marrow stem-cell pool might, therefore, represent a novel, drug-free means of slowing the age-related decline of the musculoskeletal system.

Exercise is important in stemming both osteoporosis and obesity, with the fact that MSCs are progenitors of both osteoblasts and adipocytes (fat cells), as well as the anabolic response of the skeletal system to mechanical loadings. It was then hypothesized that mechanical signals anabolic to bone would invariably cause a parallel decrease in fat production. In an in vivo setting, seven-week-old C57BL/6J mice on a normal chow diet were randomized to undergo low magnitude high frequency loading (90 Hz at 0.2 g for 15 minutes per day) or placebo treatment [71]. At 15 weeks, with no differences in food consumption between groups, in vivo CT scans showed that the abdominal fat volume of mice subjected to loading was 27% lower than that of the controls () [72, 73]. Wet weights of visceral and subcutaneous fat deposits in loading mice were correspondingly lower. Confirmed by fluorescent labeling and flow cytometry studies [72, 73], these data indicated that the influence of mechanical signals is not only on the resident bone cell (osteoblast/osteocyte) population but also on their progenitors, biasing MSC differentiation towards bone (osteoblastogenesis) and away from fat (adipogenesis). In a follow-up test of this hypothesis, mice fed with a high fat diet were subjected to low magnitude loading or placebo treatment [72, 73]. Suppression of adiposity by the mechanical signals was accompanied by a “mechanistic response” at the molecular level, which shows that loading significantly influenced MSC commitment to either osteogenic runt-related transcription factor 2 (Runx2), a transcription factor central to osteoblastogenesis, or adipogenic (peroxisome proliferator-activated receptor [PPAR]γ, a transcription factor central to adipogenesis). Runx2 expression was greater and PPARγ expression was decreased in the mice that underwent LMMs compared with controls. The PPARγ transcription factor, when absent or present as a single copy, facilitates osteogenesis at least partly through enhanced canonical Wnt signaling [74, 75], a pathway critically important to MSC entry into the osteogenic lineage and expansion of the osteoprogenitor pool. Notably, low magnitude mechanical loading treatment also resulted in a 46% increase in the size of the MSC pool () [72, 73]. These experiments, although not obviating a role for the osteoblast/osteocyte syncytium, provide evidence that bone marrow stem cells are capable of sensing exogenous mechanical signals and responding with an alteration in the cell fate that ultimately influences both the bone and fat phenotypes. Importantly, the inverse correlation of bone and fat phenotypes has increasing support in the clinical literature. Although controversial, and despite the presumption that conditions such as obesity will inherently protect the skeleton owing to increased loading events, data in humans evaluating bone-fat interactions indicate that an ever-increasing adipose burden comes at the cost of bone structure and increased risk of fracture [76].

2.4. The Role of LRP5 in Bone Responding to Mechanical Loading

LRP5 has been shown to have important functions in the mammalian skeleton. Experimental evidences have pointed LRP5 as a critical factor in translating mechanical signals into the proper skeletal response. For example, loss-of-function mutations in LRP5 have been reported to cause the autosomal recessive human disease osteoporosis-pseudoglioma syndrome (OPPG), which leads to significant reduction of BMDs, and are more susceptible to skeletal fracture and deformity [7779]. Moreover, the mechanical importance of LRP5 has been demonstrated in LRP5−/− mice, which were found with an almost complete ablation in ulnar loading-induced bone formation compared to wild-type controls [79, 80]. Multiple single nucleotide polymorphisms (SNPs), located in exons 18 and 10, have been reported, which can significantly affect the interconnection between physical activity and bone mass [79, 81]. A high bone mass (HBM) phenotype in humans was reported to be caused by certain missense mutations near the N-terminus of LRP5 [82, 83]. An LRP5 overexpression mutation is, on the other hand, associated with high bone mass and induced osteoblast proliferation [82]. Increased sensitivity to load due to a lower threshold for initiating bone formation was also reported with this mouse [83]. A recent study done by Zhong et al. showed that in vitro tension on MC3T3-E1 cells increased LRP5 gene expression at 1, 3, and 5 hours of loading [84].

2.5. MicroRNA and Its Role in Mechanotransduction in Tissue

The newly discovered microRNAs (miRNAs) are short noncoding RNAs, which can be complementary to messenger RNA (mRNA) sequences to silent gene expression by either degradation or inhibitory translation of target transcripts [85, 86]. Regulation of Runx2, bone morphogenic protein (BMP), and Wnt signaling pathways is by far the most well-studied miRNA related osteoblast function. Positive and negative regulations of miRNAs on Runx2 expression have been shown to affect skeletal morphogenesis and osteoblastogenesis [87]. Inhibition of osteoblastogenesis can result from miRNA-135 and miRNA-26a regulated BMP-2/Smad signaling pathway [88]. Activation of Wnt signaling through miRNA-29a-targeted Wnt inhibitors is upregulated during osteoblast differentiation [89]. In addition, studies have been done to investigate the miRNA function on self-renewal and lineage determination for tissue regeneration via human stromal stem cells [90, 91]. Moreover, extensive studies have also been done to assess the effects of miRNAs on osteogenic functions in committed cell lines including osteoprogenitors, osteoblasts, and osteocytic cell lines. In general, actions of miRNA may affect bone cell differentiation in either positive or negative ways [85, 91].

Recent research has gained interests in studying the transcription and microRNA regulation to better understand gene expression regulation in a mechanical loading model. Transcription factors can bind to motifs in the promoter of genes and directly affect their expression; therefore, mechanotransduction in bone may result in transcription factors alteration for regulation. Using a predictive bioinformatics algorithm, a recent study investigated the time-dependent regulatory mechanisms that governed mechanical loading-induced gene expression in bone. Axial loading was performed on the right forelimb in rodents. A linear model of gene expression was created and 44 transcription factor binding motifs and 29 microRNA binding sites were identified to predict the regulated gene expression across the time course. It may be important in controlling the loading-induced bone formation process via the time-dependent regulatory mechanisms.

2.6. Mechanotransductive Implication in Bone Tissue Engineering

Development of artificial scaffold for musculoskeletal applications could take advantage of the mechanotransduction phenomena to achieve its integrity and function, which can lead to tissue healing. Mechanical signals delivered to bone cells may be interfered by the scaffold deformation and should be taken into account. Fortunately, mechanotransduction could be used to control the proliferation and differentiation of bone cells [55, 56, 9294]. Fluid flow has been proposed as an important mechanical aspect to be considered when developing bone scaffolds [5356, 94]. Studies using bioreactors have helped us understand the phenomena of mechanotransduction used in scaffold design [92]. For example, rotating bioreactors, flow perfusion bioreactors, and other mechanical stimuli such as strain have been designed to increase mass transfer by inducing dynamic flow conditions in culture, to create osteoinductive factors on mesenchymal stem cells by the generated fluid shear stress [95], and to induce the osteogenic differentiation of mesenchymal stem cells [96], respectively. Among all, mimicking the natural bone strain to favor osteogenesis is one of the most rational aims for scaffold development. Matching of the strain histograms of a scaffold and the actual bone can be performed using microCT measurements and finite element method [55, 97, 98].

3. Summary

Functional tissue regeneration has been shown to be significantly influenced by mechanical loading and mechanotransduction under both in vitro and in vivo conditions. There are close interrelationships among bone, muscle, cellular, molecular pathways, and biomaterial remodeling by such physiological stimulation. The effects of mechanobiology may be harnessed in such a way that dynamic fluid flow stimulation can act as a mechanobiological mediator in scaffold to regulate cellular and tissue regeneration and proliferation. Such signals must be performed and conducted in a dynamic manner and potentially served as a noninvasive approach. The increase of physiological stimulation may ultimately enhance interstitial fluid flow and mechanotransduction in tissue and engineered constructs. Furthermore, dynamic stimulation, if applied at an optimal frequency, has shown the potential to attenuate osteopenia in disuse while promoting formation in osteogenesis, which may potentially serve as a biomechanical intervention for treating osteoporosis and muscle atrophy.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.


This work is kindly supported by the National Institute of Health (R01 AR52379 and R01AR61821), the US Army Medical Research and Materiel Command, the National Space Biomedical Research Institute through NASA Contract NCC 9-58. The authors would like to thank all the members in the Orthopaedic Bioengineering Research Lab, particularly Drs. Hoyan Lam, Jiqi Cheng, Wei Lin, Sardar Uddin, and Suzanne Ferreri, for their contribution to the works.