Review Article | Open Access
Functional Roles of Syk in Macrophage-Mediated Inflammatory Responses
Inflammation is a series of complex biological responses to protect the host from pathogen invasion. Chronic inflammation is considered a major cause of diseases, such as various types of inflammatory/autoimmune diseases and cancers. Spleen tyrosine kinase (Syk) was initially found to be highly expressed in hematopoietic cells and has been known to play crucial roles in adaptive immune responses. However, recent studies have reported that Syk is also involved in other biological functions, especially in innate immune responses. Although Syk has been extensively studied in adaptive immune responses, numerous studies have recently presented evidence that Syk has critical functions in macrophage-mediated inflammatory responses and is closely related to innate immune response. This review describes the characteristics of Syk-mediated signaling pathways, summarizes the recent findings supporting the crucial roles of Syk in macrophage-mediated inflammatory responses and diseases, and discusses Syk-targeted drug development for the therapy of inflammatory diseases.
Inflammation is the body’s first immune response to protect our body from harmful stimuli, such as pathogen infection, damaged cells, and irritants [1, 2]. Symptoms include recruitment of white blood cells, pain, heat, redness, swelling, tissue damages, and dysfunctions of the organs. Inflammation is classified as either acute or chronic. Acute inflammation is immediate immune responses characterized by an increase in the movement of plasma and leukocytes from the blood to the injured sites. Acute inflammation becomes chronic inflammation when the immune system cannot remove invading pathogens or when pathogens continuously invade the body. Chronic inflammation is an inflammation of prolonged duration from several weeks to years, in which active inflammation, tissue injury, and healing occur at the same time. Chronic inflammation is a leading cause of inflammatory/autoimmune diseases, such as rheumatoid arthritis (RA), Alzheimer’s diseases, systemic lupus erythematosus (SLE), asthma, psoriasis, atherosclerosis, and cancers [3–6].
Macrophages are white blood cells developed in a myeloid lineage, and differentiated from monocytes in tissues. In inflammation, macrophages have crucial functions, such as antigen presentation, phagocytosis, and immunomodulation via the production of various inflammatory mediators [7, 8]. Macrophages play a critical role in the inflammation that occurs during innate immune responses. Macrophages are activated by the binding with various stimuli, including lipopolysaccharide (LPS), cytokines (e.g., interleukin- (IL-) 1 and tumor necrosis factor- (TNF-) α), and other chemical mediators through their receptors (e.g., toll-like receptors (TLRs) and dectin-1 [9, 10]. The binding of stimuli with the receptors on macrophages initiates the stimulatory signals and activates downstream signaling molecules, such as various types of kinases [11–13]. These signals subsequently activate transcription factors, including nuclear factor-κB (NF-κB), activator protein-1 (AP-1), and cAMP response element-binding protein (CREB), resulting in the induction of the expression of proinflammatory genes (e.g., TNF-α, COX-2, and iNOS) and the secretion of inflammatory mediators (e.g., nitric oxide (NO), reactive oxygen species (ROS), and prostaglandin E2 (PGE2)) [14, 15].
Several intracellular signaling molecules are involved and activated during the inflammatory responses in macrophages. Among these signaling molecules, tyrosine kinase families have been considered as the major effector molecule. Spleen tyrosine kinase (Syk) is a nonreceptor tyrosine kinase with a molecular weight of 72 kDa. Syk binds with TLR4 and is activated by phosphorylation mainly at tyrosine residues, resulting in the transduction of stimulatory signals through the activation of various downstream signaling molecules. Since Syk is one of upstream signaling molecules, it orchestrates many downstream signaling molecules and amplifies inflammatory signals. Therefore, Syk has been considered to play critical roles in inflammatory responses.
This review presents a general introduction to Syk as a signaling molecule, discusses the role of Syk in macrophage-mediated inflammatory responses, and summarizes Syk-related inflammatory diseases and Syk inhibitors that could be candidates for the treatment of these diseases. This aim of this review is to increase understanding of the role of Syk in macrophage-mediated inflammatory responses in order to support the development of new therapeutic drugs for the treatment of macrophage-mediated inflammatory diseases.
2. Structure and Functions of Syk
2.1. Structure of Syk and Its Posttranslational Modifications
Syk is a 72 kDa nonreceptor type of tyrosine kinase consisting of two tandem repeat of Src homology 2 (SH2) domains and one C-terminus kinase domain. These domains are connected with two interdomains: interdomain A between two SH2 domains and interdomain B between C-terminus SH2 domain and a kinase domain (Figure 1(a)) [16–18]. Syk has two forms: the original Syk and an alternatively spliced form called Syk-B that lacks 23 amino acids in interdomain B, including nuclear localization signal peptide (Figure 1(a)) [19, 20]. Although the Syk-B form is found in cells, the exact mechanisms of alternative slicing have not yet been well elucidated. The structure of Syk family kinases among species is highly conserved. Like human Syk, mouse Syk consists of two SH2 domains and a kinase domain at C-terminus . Mouse Syk is only 6 amino acids shorter than human Syk and 92% homologous with human Syk in amino acid sequences. The fruit fly, Drosophila melanogaster, has a Syk-related molecule named SH2 domain ankyrin repeat kinase (SHARK), which consist of two SH2 domains and a kinase domain at C-terminus, and unlike Syk, SHARK has ankyrin-like repeats (ANKs) in interdomain A . Hydra has two Syk-like molecules: HTK98 is similar to human Syk, but HTK is more similar to fruit fly Syk, SHARK [23, 24]. Interestingly, the worm Caenorhabditis elegans does not have a Syk-like molecule . Mammalian cells express another type of Syk family kinase named zeta-chain-associated protein kinase of 70 kDa (ZAP70) (Figure 1(a)). ZAP70 has almost the same structure as that of Syk, consisting of two SH2 domains and a kinase domain, but shows low homology to Syk in amino acid sequences (less than 50%) and its expression is restricted in certain cell types, such as T cells and NK cells . The characteristics of the Syk family of kinases are summarized in Table 1.
Posttranslational modifications are modifications in the protein synthesis process and are critical steps for the regulation of protein activity. Syk also has posttranslational modifications. Syk is ubiquitinated by Cbl-b and undergoes proteasomal degradation, which negatively regulates B-cell receptor signaling . More importantly, phosphorylation is the most abundant posttranslational modification in Syk. It has been reported that ten sites of Syk are autophosphorylated (Figure 1(b)): one site located in the N-terminal between two SH2 domains, five sites located in the interdomain region between the C-terminal SH2 domain and the kinase domain, two sites located in the kinase domain, and two sites at C-terminus . Syk is phosphorylated on tyrosine residue 317 by Lyn, a Src-phosphotyrosine kinase [27, 28]. Syk is phosphorylated on multiple tyrosine sites, including Tyr317, Tyr342, and Tyr346 in interdomain B under the condition of binding with B-cell receptor , and phosphorylated on Tyr630 of human Syk to create binding site for BLNK . Syk is also phosphorylated on serine residues. Phosphorylation of Syk on Ser297 is observed within 5 min after the stimulation of B-cell receptor . Unlike ubiquitination and phosphorylation, other types of posttranslational modifications of Syk, such as methylation and acetylation, have not yet been clearly reported.
2.2. Localization and Tissue Specificity of Syk
Syk localizes mostly in cytoplasm . As previously reported, Syk interacts with a number of proteins mainly located in cytoplasm or plasma membrane, implying that the fraction where Syk is mainly located is cytoplasm. However, Syk is also found in the nucleus . Syk was reported to be translocated from nucleus to plasma membrane to interact with B-cell receptor under the activation of B-cell receptor . Although Syk is found in both nucleus and cytoplasm, the exact molecular mechanisms that trigger the translocation of Syk from nucleus to cytoplasm or in the reverse direction have not yet been well elucidated.
Following an initial report of being highly expressed in hematopoietic cells , Syk was thought to be a hematopoietic cell-specific kinase. Later studies, however, reported that Syk is widely expressed in nonhematopoietic cells, including epithelial cells, fibroblasts, and neuronal and vascular endothelial cells [34, 35]. Interestingly, Syk is highly expressed in peritoneal macrophages and Raw 264.7 cells, a murine macrophage-like cell line. Under the stimulation of cells by various TLR ligands, such as LPS, poly I:C, and Pam3CSK4, Syk is highly activated within several minutes , implying that it plays a pivotal role in macrophage-mediated innate immunity through TLRs.
2.3. Syk-Binding Proteins
Identification of Syk-binding proteins is critical because activation of Syk is induced by a number of physiological ligands. Along with the activation of Syk by autophosphorylation, Syk is also activated by phosphorylation through the binding with upstream kinases and activated Syk binds with downstream substrate proteins to transduce its signaling. Proteome analysis using amine-specific isotope tag and GFP nanotrap identified Syk-binding proteins with high efficiency and affinity, such as CrkL, BLNK, tubulins, Csk, RanBP5, and DJ-1 . Several upstream kinases have been identified to bind with and then activate Syk. Lyn binds and phosphorylates with Syk . RhoH, an atypical G protein, binds with Syk and is followed by Syk activation . Nuclear factor of activated T cells- (NFAT-) activating molecule 1 (NFAM1), which is an ITAM-containing cell surface molecule, also binds with Syk through its phosphorylated ITAM motif . TLR binds with Syk and regulates signaling . Syk also binds with the following of its downstream proteins: (1) adapter proteins, such as linker for activation of T cells (LAT) , SH2 domain-containing leukocyte protein of 76 kDa (SLP-76) , B-cell linker protein (BLNK) , B-cell adaptor for PI3K (BCAP) , HS-1 (also known as SPY75) , Src homology and collagen (SHC) , and T-cell receptor (TCR  and 3BP2 ); (2) enzymes, such as Cb1 , phospholipase C-γ (PLC-γ) , phospholipase D (PLD) , Bruton’s tyrosine kinase (BTK) , proline-rich tyrosine kinase 2 (PYK2) , Vav1 , phosphatidylinositol 3 kinase (PI3K) , mitogen-activated protein kinases (MAPK), extracellular signal-regulated kinase (ERK), and janus kinase (JNK) [56–58]; and (3) cytoskeletal components and cell adhesion molecules, such as tubulin , SH3 domain-containing protein 7 (SH3P7) , and β-integrins [61, 62].
2.4. Roles of Syk in Signal Transduction
Syk plays a critical role in immunoreceptor signaling pathways. Many immunoreceptors, including B-cell receptor, T-cell receptor, and various FcRs, contain immunoreceptor tyrosine-based activation motifs (ITAMs) in their cytoplasmic domains, and the ITAMs are phosphorylated by Src-family kinases. The first step of Syk activation is its binding to phosphorylated ITAMs of the immunoreceptors. Once ITAMs are phosphorylated by Src-family kinases, Syk is recruited to the phosphorylated ITAMs and binds with phosphorylated tyrosine residues in ITAMs through its SH2 domains. This binding leads to conformational change and unfolding of Syk, resulting in consequent activation of Syk through the autophosphorylation itself as well as the phosphorylation by other upstream kinases, such as Lyn . The activated Syk which gains an enzymatic activity transduces its signaling cascades to downstream through activating its downstream substrate proteins by phosphorylating them and sometimes even directly interacting them. Therefore, most critical events for initiating Syk activation are the phosphorylation of ITAMs in immunoreceptors and subsequent binding of Syk to the phosphorylated ITAMs through its SH2 domains. As described in Section 2.3, Syk binds with a variety of upstream signaling molecules and its downstream substrates, and these interactions activate Syk-mediated signaling pathways.
Syk is involved in cell adhesion molecule signaling. In vitro and in vivo studies show that Syk is activated in integrin signaling transduction, resulting in the increase in adhesion of leukocytes to the inflamed endothelial cells [63–65]. Syk also interacts with P-selectin glycoprotein ligand 1 (PSGL1) through ITAM motifs of PSGL1. With the interaction of Syk with PSGL1, Syk is subsequently activated in the PSGL1 signal transduction pathway in leukocytes [66, 67], and inhibition of Syk activity results in the suppression of PSGL1-mediated transcriptional regulation .
Syk shows its roles in innate pathogen recognition. Recently, several studies have reported that Syk is a key molecule in the signaling pathways initiated by pattern recognition receptors (PRRs) in terms of recognizing pathogen-associated molecule patterns (PAMPs) and activating innate immune responses mediated by Syk is activated through the interaction with C-type lectin CLEC7A, which is a mammalian PRR for fungal β-glucans , and this Syk-CLEC7A interaction stimulates its signaling pathways, resulting in the production of ROS [69, 70] and phagocytosis of yeast by dendritic cells . Syk is also activated in the signaling pathways triggered by the recognition of bacteria and viruses. The binding of mycobacterial PAMPs to their receptors, CLEC7A, CLEC6A, or CLEC4E, stimulates Syk activation in their signal transduction , and Syk knock-out mice show attenuated antibacterial host defense . The binding of dengue virus to its receptor, CLEC5A, activates Syk and induces the production of proinflammatory cytokines through the binding of Syk with phosphorylated DAP12, which is an adaptor molecule between CLEC5A and Syk .
Syk is also activated through nonpathogenic stimuli, such as the molecules produced from damaged cells. The ligands produced by necrotic cells bind to their receptors, such as CLEC4E associated with FcγR or CLEC9A, resulting in the recruitment and activation of Syk [74–76]. Interestingly, Syk is involved in the signaling of the FcγR-mediated, antibody-dependent cellular cytotoxicity (ADCC) reaction. The FcγR-mediated ADCC reaction is suppressed in Syk and ZAP70-defective natural killer cells, implying that Syk plays a critical role for a FcγR-mediated ADCC reaction .
3. Functions of Syk in Macrophage-Mediated Inflammatory Responses and Diseases
Although the functions of Syk have been intensively studied in adaptive immune responses, especially in B-cell signaling, its functions in other types of cells, such as macrophages, have also been studied. This section examines the functions of Syk in macrophage-mediated inflammatory responses.
Macrophages function as the first line of defense against invading pathogens. Macrophages use cell surface receptors to detect the pathogens, for example, PRRs such as TLRs, to initiate signaling inside the cells, and then to activate appropriate immune responses through its cytoplasmic domain. One of the most critical molecules in innate immune responses is intracellular nonreceptor tyrosine kinases, such as Syk, which is the only Syk family kinase found in innate cells.
Syk is involved in TLR4 signaling (Figure 2). Syk is recruited to TLR4 in macrophages  and binds with TLR4 through its N-terminal SH2 domain . Syk is activated in macrophages under LPS stimulation. Syk is very quickly activated (within 2 min) by phosphorylation under LPS stimulation condition. Syk activation leads to the subsequent activation of downstream signaling molecules, such as p85, AKT, IKK, PDK1, and NF-κB, resulting in the induction of expression of proinflammatory genes, such as TNF-α, COX-2, and iNOS, and the production of inflammatory mediators, such as NO and PGE2 in macrophages [80–83]. Syk is also activated by minimally oxidized low-density lipoprotein (mmLDL). Once mmLDL binds to TLR4, Syk binds with LTR4 and is activated, and subsequently activates Vav1, PLC-γ, and JNK, resulting in cytoskeleton rearrangement, ROS generation, and cytokine secretion in macrophages . Since Syk activation induces inflammatory responses in macrophages, a number of previous studies have shown that Syk inhibition suppresses inflammatory responses in macrophages. A variety of plant extracts has been reported to suppress inflammatory responses through the inhibition of Syk activity. The ethanol extract of Cinnamomum cassia suppresses the production of NO, PGE2, and TNF-α in LPS-stimulated macrophages . The methanol extract of Evodia lepta suppresses the production of NO and PGE2 in LPS-stimulated macrophages and ameliorates the symptoms of EtOH/HCl-induced gastritis . The ethanol extract of Artemisia asiatica, the methanol extract of Cerbera manghas, and the methanol extract of Hopea odorata also suppress the production of NO, PGE2, and TNF-α in LPS-stimulated macrophages and ameliorate the symptoms of EtOH/HCl-induced gastritis [85–87]. The methanol extract of Archidendron clypearia suppresses the production of NO, PGE2, and TNF-α in LPS-stimulated macrophages and ameliorates the symptoms of dextran sodium sulfate (DSS)-induced colitis . The ethanol extract of Myrsine seguinii also suppresses the production of NO, PGE2, and TNF-α in LPS-stimulated macrophages and ameliorates the symptoms of thioglycollate-induced peritonitis . The methanol extract of Rhodomyrtus tomentosa suppresses the production of NO and PGE2 in LPS-stimulated macrophages and ameliorates the symptoms of EtOH/HCl-induced gastritis and DSS-induced colitis . Single compounds or chemicals also suppress inflammatory responses through the inhibition of Syk activity. Piceatannol, a pharmacological inhibitor of Syk, strongly suppresses inflammatory responses , and caffeic acid, which inhibits Syk activation, suppresses inflammatory responses in macrophages . Quercetin, a major bioflavonoid present in fruits and vegetables, also inhibits Syk activation, resulting in the suppression of inflammatory responses in macrophages . The plant extracts and natural compounds that suppress macrophage-mediated inflammatory responses through the inhibition of Syk are summarized in Table 2. On the contrary to the majority of previous studies that Syk activation induces inflammatory responses in macrophages, Syk was also reported to have a suppressive role in inflammatory responses. The secretion of proinflammatory cytokines, such as TNF, IL-6, and IL-12 was dramatically increased in Syk-deficient bone marrow-derived macrophages compared to wild type macrophages in response to various TLR ligands, including LPS, CpG DNA, and lipopeptide . These results were supported by another result that the secretion of above proinflammatory cytokines was also increased in the bone marrow-derived macrophages lacking DAP12 which is an upstream signal cascade molecule of Syk compared to wild type macrophages in the response of TLR ligands . Although this observation is contradictory to a lot of previous studies, it might be possible in the aspects that the bone marrow-derived macrophages used in this study were generated from Syk-deficient fetal liver chimeras because Syk-deficient mice are embryonic lethal ; therefore, the function of Syk in these macrophages might be different from that of conventional effector macrophages in inflammatory lesions. Moreover, the doses of TLR ligands used in this study to stimulate bone marrow-derived macrophages seem relatively low, whereas the doses in other studies which showed a stimulatory role of Syk in inflammatory responses in RAW264.7 cells and peritoneal macrophages were relatively high and widely used levels; in addition, the secretion of the proinflammatory cytokines did not show clear dose-dependency with TLR ligands, implying that the role of Syk in macrophage-mediated inflammatory response might be also different depending on the doses of TLR stimulatory ligands. Taken together, these findings strongly support the crucial role played by Syk in macrophage-mediated inflammatory responses.
4. Syk-Targeted Drug Development
4.1. Syk Inhibitors
Since Syk plays a crucial role in B-cell activation and in innate immune cell-mediated immune responses, especially macrophage-mediated inflammatory responses which subsequently contribute to the pathogenesis of various diseases, several Syk inhibitors have been actively developed, some of which are currently in clinical trials to treat human diseases. This section examines the Syk inhibitors that have been developed and are under development.
Most Syk inhibitors are synthetic derivatives. Various types of nuclei, such as naphthyridines, pyrimidine-5-carboxamide, imidazole[1,2-c]pyrimidine, 1,2,4-triazolo[4,3-c]pyrimidine, 4-thiazolyl-2-phenylaminopyrimidines, and oxindoles, have been modified to increase their inhibitory potencies against Syk. Naphthyridine is a basic nucleus that shows Syk inhibitory activity. Seventeen derivatives of this compound have been developed to increase the inhibitory potency, and their IC50 values range from 90 μM to several nM . Pyrimidine-5-carboxamide shows Syk-specific inhibitory potency. Eleven derivatives of pyrimidine-5-carboxamide have been synthesized with IC50 values ranging from over 10 μM to 23 nM . Imidazole[1,2-c]pyrimidine has seven derivatives with IC50 values ranging from over 7.1 μM to 6 nM, and 1,2,4-triazolo[4,3-c]pyrimidine has six derivatives with IC50 values ranging from over 7.7 μM to 4 nM . Six derivatives of 4-thiazolyl-2-phenylaminopyrimidines have been developed with IC50 values ranging from 1.8 μM to 4 nM, and five derivatives of oxindoles have been developed with IC50 values ranging from 8.1 μM to 5 nM .
Natural Syk inhibitors, such as curcumin and piceatannol, have also been reported. Curcumin inhibits Syk signaling pathways and could be used in the treatment of B-cell lymphoma . Piceatannol also inhibits Syk activity, but its inhibitory action has not yet been well elucidated . Several Syk inhibitors are currently in clinical trials (Table 3). R406, R788, R112, and R343 are structurally related analogues that are selective ATP-competitive Syk inhibitors; they were developed to treat a variety of inflammatory and allergic diseases [3, 95]. BAY-61-3606, identified by Yamamoto et al., is an imidazopyrimidine analogue that selectively inhibits Syk activity to treat allergic diseases . Pyrimidine-5-carboxamides families, such as YM193306 and other derivatives developed by Hisamichi et al. are also Syk inhibitors to treat allergic diseases .
4.2. Syk in Inflammatory Diseases and Syk-Targeted Therapeutics
Many studies using in vivo animal models and Syk knock-out experiments have demonstrated that Syk is involved in various inflammatory diseases, such as RA, allergic asthma/rhinitis, intestinal ischemia reperfusion injury, SLE, and idiopathic thrombocytopenic purpura (ITP), and that Syk inhibition could be a therapeutic strategy for the treatment of these inflammatory diseases [98–103]. Syk is expressed and activated in the synovium of RA . Activated Syk increases TNF-α-induced cytokine expression through the suppression of JNK signaling in fibroblast-like synoviocytes . Moreover, several studies have revealed that Syk plays a pathological role in animal models of arthritis [105–107]. An orally available drug, R406, and R788, a prodrug of R406, show antiarthritic effects in the collagen-induce arthritis animal model , and immunotherapy treatment of RA targeting activated macrophages where Syk is activated ameliorates the arthritic symptoms in an animal model . Moreover, these two drugs are in clinical trial phase II for the treatment of RA and show significant effects in the patients with active RA . Syk is involved in allergic conditions, such as allergic rhinitis and asthma, through the activation of IgE production. Syk is critical for activating the mediators of degranulation, eicosanoid, and cytokine production . R112 inhibits IgE-mediated histamine release from human basophils , and its intranasal administration significantly decreases the clinical symptoms of allergic rhinitis in clinical trial phase II . R343 developed most recently is in clinical trial phase I with an inhaled formulation for the treatment of allergic asthma . Hematopoietic cells are involved in the expression of ischemia reperfusion injury, implying that targeting Syk could be applied to the treatment of ischemia reperfusion injury . R788 has been reported to suppress the symptoms of ischemia reperfusion injury in an animal model [113, 114]. Syk is also involved in the pathogenesis of SLE. The pathogenesis of SLE correlates to B-cell activation where Syk could play a critical role . The symptoms of SLE are ameliorated by the R788 in lupus-prone MRL/lps and BAX/BAK mice [116, 117]. ITP is mediated by the production of IgG specific for antigens on platelets. Since Syk is involved in FcgR-mediated signaling activation, it may participate in this disease. Indeed, the Syk inhibitors R406 and R788 ameliorated the symptoms of ITP in an animal model  and in human clinical trials. In addition to these inflammatory diseases, Syk may play a critical role in activated macrophage-mediated inflammatory diseases, including Crohn’s disease, psoriasis, and atherosclerosis, since Syk is a critical kinase for macrophage-mediated inflammatory responses. Another orally administrable, selective Syk inhibitor, BAY-61-3606, exhibits an inhibitory effect of degranulation and cytokine synthesis in mast cells and suppresses the symptoms of antigen-induced airway inflammation, including asthma and rhinitis, in in vivo animal models . However, Bay-61-6303 exhibits its target selectivity profile limiting to only 6 kinases and shows significant off-target effects , implying that BAY-61-6306 may not be a good candidate for clinical trials and drug development.
5. Conclusions and Perspective
Although inflammation is the process of protecting our body from invading pathogens, excessive and chronic inflammatory responses are major causes of various types of diseases, including inflammatory/autoimmune diseases and cancers. Increasing evidence has revealed that activated macrophages are major effector cells in inflammatory responses and inflammatory diseases. Several studies have demonstrated that Syk is critically involved in macrophage-mediated inflammatory responses and in inflammatory diseases, including RA, allergic asthma/rhinitis, SLE, intestinal ischemia reperfusion injury, and ITP. This implies that Syk is a crucial player in inflammatory responses and could be a potent target to treat inflammatory diseases. Although many Syk inhibitors have been and are being developed, most suffer shortcomings such as cytotoxicity, low therapeutic efficacies, and off-target effects due to multiple kinase targeting. This necessitates the development of new potential Syk inhibitors with properties that offer both lower cytotoxicity and higher therapeutic efficacy. We expect novel Syk inhibitors, especially novel biological drugs that selectively target Syk, with strong anti-inflammatory effects and minimal toxicity, to be developed for the treatment of macrophage-mediated inflammatory diseases in the near future.
Conflict of Interests
The authors report no conflict of interests. The authors alone are responsible for the content and writing of the paper.
Young-Su Yi and Young-Jin Son equally contributed to this work.
This work was carried out with the support of the “Cooperative Research Program for Agriculture Science & Technology Development (Project no. PJ009241),” Rural Development Administration, Korea.
- L. Ferrero-Miliani, O. H. Nielsen, P. S. Andersen, and S. E. Girardin, “Chronic inflammation: importance of NOD2 and NALP3 in interleukin-1β generation,” Clinical and Experimental Immunology, vol. 147, no. 2, pp. 227–235, 2007.
- H. Kayama, J. Nishimura, and K. Takeda, “Regulation of intestinal homeostasis by innate immune cells,” Immune Network, vol. 13, no. 6, pp. 227–234, 2013.
- M. Kaur, M. Singh, and O. Silakari, “Inhibitors of switch kinase “spleen tyrosine kinase” in inflammation and immune-mediated disorders: a review,” European Journal of Medicinal Chemistry, vol. 67, pp. 434–446, 2013.
- Y. I. Cha and H. S. Kim, “Emerging role of sirtuins on tumorigenesis: possible link between aging and cancer,” BMB Reports, vol. 46, no. 9, pp. 429–438, 2013.
- M. H. Park and K. Igarashi, “Polyamines and their metabolites as diagnostic Markers of human diseases,” Biomolecules & Therapeutics, vol. 21, no. 1, pp. 1–9, 2013.
- M. Ham and A. Moon, “Inflammatory and microenvironmental factors involved in breast cancer progression,” Archives of Pharmacal Research, vol. 36, no. 12, pp. 1419–1431, 2013.
- J. Lee, “Adipose tissue macrophages in the development of obesity-induced inflammation, insulin resistance and type 2 diabetes,” Archives of Pharmacal Research, vol. 36, no. 2, pp. 208–222, 2013.
- J. W. Jeon, B. C. Park, J. G. Jung, Y. S. Jang, E. C. Shin, and Y. W. Park, “The soluble form of the cellular prion protein enhances phagocytic activity and cytokine production by human monocytes via activation of ERK and NF-κB,” Immune Network, vol. 13, no. 4, pp. 148–156, 2013.
- P. R. Taylor, L. Martinez-Pomares, M. Stacey, H.-H. Lin, G. D. Brown, and S. Gordon, “Macrophage receptors and immune recognition,” Annual Review of Immunology, vol. 23, pp. 901–944, 2005.
- J. Han, J.-D. Lee, L. Bibbs, and R. J. Ulevitch, “A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells,” Science, vol. 265, no. 5173, pp. 808–811, 1994.
- T. Yu, Y.-S. Yi, Y. Yang, J. Oh, D. Jeong, and J. Y. Cho, “The pivotal role of TBK1 in inflammatory responses mediated by macrophages,” Mediators of Inflammation, vol. 2012, Article ID 979105, 8 pages, 2012.
- S. E. Byeon, Y.-S. Yi, J. Oh, B. C. Yoo, S. Hong, and J. Y. Cho, “The role of Src kinase in macrophage-mediated inflammatory responses,” Mediators of Inflammation, vol. 2012, Article ID 512926, 18 pages, 2012.
- J.-E. Cho, S. Park, H. Lee, S.-N. Cho, and Y. S. Kim, “Mycobacterium tuberculosis-induced expression of granulocyte-macrophage colony stimulating factor is mediated by PI3-K/MEK1/p38 MAPK signaling pathway,” BMB Reports, vol. 46, no. 4, pp. 213–218, 2013.
- J.-W. Lee, N. H. Kim, J.-Y. Kim et al., “Aromadendrin inhibits lipopolysaccharide-induced nuclear translocation of NF-κB and phosphorylation of JNK in RAW 264.7 macrophage cells,” Biomolecules & Therapeutics, vol. 21, no. 3, pp. 216–221, 2013.
- Y. Duan, F. Chen, A. Zhang et al., “Aspirin inhibits lipopolysaccharide-induced COX-2 expression and PGE2 production in porcine alveolar macrophages by modulating protein kinase C and protein tyrosine phosphatase activity,” BMB Reports, vol. 47, no. 1, pp. 45–50, 2014.
- T. Taniguchi, T. Kobayashi, J. Kondo et al., “Molecular cloning of a porcine gene syk that encodes a 72-kDa protein-tyrosine kinase showing high susceptibility to proteolysis,” The Journal of Biological Chemistry, vol. 266, no. 24, pp. 15790–15796, 1991.
- K. Fütterer, J. Wong, R. A. Grucza, A. C. Chan, and G. Waksman, “Structural basis for Syk tyrosine kinase ubiquity in signal transduction pathways revealed by the crystal structure of its regulatory SH2 domains bound to a dually phosphorylated ITAM peptide,” Journal of Molecular Biology, vol. 281, no. 3, pp. 523–537, 1998.
- A. Mócsai, J. Ruland, and V. L. J. Tybulewicz, “The SYK tyrosine kinase: a crucial player in diverse biological functions,” Nature Reviews Immunology, vol. 10, no. 6, pp. 387–402, 2010.
- M. Turner, E. Schweighoffer, F. Colucci, J. P. di Santo, and V. L. Tybulewicz, “Tyrosine kinase Syk: essential functions for immunoreceptor signalling,” Immunology Today, vol. 21, no. 3, pp. 148–154, 2000.
- L. Wang, L. Duke, P. S. Zhang et al., “Alternative splicing disrupts a nuclear localization signal in spleen tyrosine kinase that is required for invasion suppression in breast cancer,” Cancer Research, vol. 63, no. 15, pp. 4724–4730, 2003.
- A.-C. Andres, G. Zuercher, V. Djonov, M. Flueck, and A. Ziemiecki, “Protein tyrosine kinase expression during the estrous cycle and carcinogenesis of the mammary gland,” International Journal of Cancer, vol. 63, no. 2, pp. 288–296, 1995.
- J. S. Ziegenfuss, R. Biswas, M. A. Avery et al., “Draper-dependent glial phagocytic activity is mediated by Src and Syk family kinase signalling,” Nature, vol. 453, no. 7197, pp. 935–939, 2008.
- R. E. Steele, N. A. Stover, and M. Sakaguchi, “Appearance and disappearance of Syk family protein-tyrosine kinase genes during metazoan evolution,” Gene, vol. 239, no. 1, pp. 91–97, 1999.
- H. Suga, M. Koyanagi, D. Hoshiyama et al., “Extensive gene duplication in the early evolution of animals before the parazoan-eumetazoan split demonstrated by G proteins and protein tyrosine kinases from sponge and hydra,” Journal of Molecular Evolution, vol. 48, no. 6, pp. 646–653, 1999.
- H. W. Sohn, H. Gu, and S. K. Pierce, “Cbl-b negatively regulates B cell antigen receptor signaling in mature B cells through ubiquitination of the tyrosine kinase Syk,” Journal of Experimental Medicine, vol. 197, no. 11, pp. 1511–1524, 2003.
- M. T. Furlong, A. M. Mahrenholz, K.-H. Kim, C. L. Ashendel, M. L. Harrison, and R. L. Geahlen, “Identification of the major site of autophosphorylation of the murine protein-tyrosine kinase Syk,” Biochimica et Biophysica Acta—Molecular Cell Research, vol. 1355, no. 2, pp. 177–190, 1997.
- T. Kurosaki, M. Takata, Y. Yamanashi et al., “Syk activation by the Src-family tyrosine kinase in the B cell receptor signaling,” Journal of Experimental Medicine, vol. 179, no. 5, pp. 1725–1729, 1994.
- J. J. Hong, T. M. Yankee, M. L. Harrison, and R. L. Geahlen, “Regulation of signaling in B cells through the phosphorylation of Syk on linker region tyrosines: a mechanism for negative signaling by the Lyn tyrosine kinase,” The Journal of Biological Chemistry, vol. 277, no. 35, pp. 31703–31714, 2002.
- L. M. Keshvara, C. C. Isaacson, T. M. Yankee, R. Sarac, M. L. Harrison, and R. L. Geahlen, “Syk- and Lyn-dependent phosphorylation of Syk on multiple tyrosines following B cell activation includes a site that negatively regulates signaling,” Journal of Immunology, vol. 161, no. 10, pp. 5276–5283, 1998.
- D. Cox and S. Greenberg, “Phagocytic signaling strategies: Fcγ receptor-mediated phagocytosis as a model system,” Seminars in Immunology, vol. 13, no. 6, pp. 339–345, 2001.
- H. Bohnenberger, T. Oellerich, M. Engelke, H.-H. Hsiao, H. Urlaub, and J. Wienands, “Complex phosphorylation dynamics control the composition of the Syk interactome in B cells,” European Journal of Immunology, vol. 41, no. 6, pp. 1550–1562, 2011.
- Y. Kulathu, G. Grothe, and M. Reth, “Autoinhibition and adapter function of Syk,” Immunological Reviews, vol. 232, no. 1, pp. 286–299, 2009.
- H. Ma, T. M. Yankee, J. Hu, D. J. Asai, M. L. Harrison, and R. L. Geahlen, “Visualization of Syk-antigen receptor interactions using green fluorescent protein: differential roles for Syk and Lyn in the regulation of receptor capping and internalization,” Journal of Immunology, vol. 166, no. 3, pp. 1507–1516, 2001.
- S. Yanagi, T. Kurosaki, and H. Yamamura, “The structure and function of nonreceptor tyrosine kinase p72SYK expressed in hematopoietic cells,” Cellular Signalling, vol. 7, no. 3, pp. 185–193, 1995.
- S. Yanagi, R. Inatome, T. Takano, and H. Yamamura, “Syk expression and novel function in a wide variety of tissues,” Biochemical and Biophysical Research Communications, vol. 288, no. 3, pp. 495–498, 2001.
- Y. G. Lee, B. M. Chain, and J. Y. Cho, “Distinct role of spleen tyrosine kinase in the early phosphorylation of inhibitor of κBα via activation of the phosphoinositide-3-kinase and Akt pathways,” The International Journal of Biochemistry and Cell Biology, vol. 41, no. 4, pp. 811–821, 2009.
- J. A. Galan, L. L. Paris, H.-J. Zhang, J. Adler, R. L. Geahlen, and W. A. Tao, “Proteomic studies of Syk-interacting proteins using a novel amine-specific isotope tag and GFP nanotrap,” Journal of the American Society for Mass Spectrometry, vol. 22, no. 2, pp. 319–328, 2011.
- H. Oda, M. Fujimoto, M. S. Patrick et al., “RhoH plays critical roles in Fc epsilon RI-dependent signal transduction in mast cells,” Journal of Immunology, vol. 182, no. 2, pp. 957–962, 2009.
- M. Ohtsuka, H. Arase, A. Takeuchi et al., “NFAM1, an immunoreceptor tyrosine-based activation motif-bearing molecule that regulates B cell development and signaling,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 21, pp. 8126–8131, 2004.
- A. Chaudhary, T. M. Fresquez, and M. J. Naranjo, “Tyrosine kinase Syk associates with toll-like receptor 4 and regulates signaling in human monocytic cells,” Immunology and Cell Biology, vol. 85, no. 3, pp. 249–256, 2007.
- S. Saitoh, R. Arudchandran, T. S. Manetz et al., “LAT is essential for Fc(epsilon)RI-mediated mast cell activation,” Immunity, vol. 12, no. 5, pp. 525–535, 2000.
- L. R. Hendricks-Taylor, D. G. Motto, J. Zhang, R. P. Siraganian, and G. A. Koretzky, “SLP-76 is a substrate of the high affinity IgE receptor-stimulated protein tyrosine kinases in rat basophilic leukemia cells,” The Journal of Biological Chemistry, vol. 272, no. 2, pp. 1363–1367, 1997.
- C. Fu, C. W. Turck, T. Kurosaki, and A. C. Chan, “BLNK: a central linker protein in B cell activation,” Immunity, vol. 9, no. 1, pp. 93–103, 1998.
- T. Okada, A. Maeda, A. Iwamatsu, K. Gotoh, and T. Kurosaki, “BCAP: the tyrosine kinase substrate that connects B cell receptor to phosphoinositide 3-kinase activation,” Immunity, vol. 13, no. 6, pp. 817–827, 2000.
- Y. Yamanashi, T. Fukuda, H. Nishizumi et al., “Role of tyrosine phosphorylation of HS1 in B cell antigen receptor-mediated apoptosis,” Journal of Experimental Medicine, vol. 185, no. 7, pp. 1387–1392, 1997.
- K. Nagai, M. Takata, H. Yamamura, and T. Kurosaki, “Tyrosine phosphorylation of Shc is mediated through Lyn and Syk in B cell receptor signaling,” The Journal of Biological Chemistry, vol. 270, no. 12, pp. 6824–6829, 1995.
- S. Latour, M. Fournel, and A. Veillette, “Regulation of T-cell antigen receptor signalling by Syk tyrosine protein kinase,” Molecular and Cellular Biology, vol. 17, no. 8, pp. 4434–4441, 1997.
- M. Deckert, S. Tartare-Deckert, J. Hernandez, R. Rottapel, and A. Altman, “Adaptor function for the Syk kinases-interacting protein 3BP2 in IL-2 gene activation,” Immunity, vol. 9, no. 5, pp. 595–605, 1998.
- M. L. Lupher Jr., N. Rao, N. L. Lill et al., “Cbl-mediated negative regulation of the Syk tyrosine kinase: a critical role for Cbl phosphotyrosine-binding domain binding to Syk phosphotyrosine 323,” The Journal of Biological Chemistry, vol. 273, no. 52, pp. 35273–35281, 1998.
- M. Takata, H. Sabe, A. Hata et al., “Tyrosine kinases Lyn and Syk regulate B cell receptor-coupled Ca2+ mobilization through distinct pathways,” The EMBO Journal, vol. 13, no. 6, pp. 1341–1349, 1994.
- T. Hitomi, S. Yanagi, R. Inatome, and H. Yamamura, “Cross-linking of the B cell receptor induces activation of phospholipase D through Syk, Btk and phospholipase C-γ2,” FEBS Letters, vol. 445, no. 2-3, pp. 371–374, 1999.
- Y. Kawakami, J. Kitaura, S. E. Hartman, C. A. Lowell, R. P. Siraganian, and T. Kawakami, “Regulation of protein kinase CβI by two protein-tyrosine kinases, Btk and Syk,” Proceedings of the National Academy of Sciences of the United States of America, vol. 97, no. 13, pp. 7423–7428, 2000.
- H. Okazaki, J. Zhang, M. M. Hamawy, and R. P. Siraganian, “Activation of protein-tyrosine kinase Pyk2 is downstream of Syk in FcεRI signaling,” The Journal of Biological Chemistry, vol. 272, no. 51, pp. 32443–32447, 1997.
- R. Arudchandran, M. J. Brown, M. J. Peirce et al., “The Src homology 2 domain of Vav is required for its compartmentation to the plasma membrane and activation of c-Jun NH2-terminal kinase 1,” The Journal of Experimental Medicine, vol. 191, no. 1, pp. 47–60, 2000.
- L. O. Beitz, D. A. Fruman, T. Kurosaki, L. C. Cantley, and A. M. Scharenberg, “SYK is upstream of phosphoinositide 3-kinase in B cell receptor signaling,” The Journal of Biological Chemistry, vol. 274, no. 46, pp. 32662–32666, 1999.
- P. S. Costello, M. Turner, A. E. Walters et al., “Critical role for the tyrosine kinase Syk in signalling through the high affinity IgE receptor of mast cells,” Oncogene, vol. 13, no. 12, pp. 2595–2605, 1996.
- J. Zhang, E. H. Berenstein, R. L. Evans, and R. P. Siraganian, “Transfection of Syk protein tyrosine kinase reconstitutes high affinity IgE receptor-mediated degranulation in a Syk-negative variant of rat basophilic leukemia RBL-2H3 cells,” Journal of Experimental Medicine, vol. 184, no. 1, pp. 71–79, 1996.
- N. Hirasawa, A. Scharenberg, H. Yamamura, M. A. Beaven, and J.-P. Kinet, “A requirement for Syk in the activation of the microtubule-associated protein kinase/phospholipase A2 pathway by FcεR1 is not shared by a G protein-coupled receptor,” The Journal of Biological Chemistry, vol. 270, no. 18, pp. 10960–10967, 1995.
- J. D. Peters, M. T. Furlong, D. J. Asai, M. L. Harrison, and R. L. Geahlen, “Syk, activated by cross-linking the B-cell antigen receptor, localizes to the cytosol where it interacts with and phosphorylates α-tubulin on tyrosine,” The Journal of Biological Chemistry, vol. 271, no. 9, pp. 4755–4762, 1996.
- O. Larbolette, B. Wollscheid, J. Schweikert, P. J. Nielsen, and J. Wienands, “SH3P7 is a cytoskeleton adapter protein and is coupled to signal transduction from lymphocyte antigen receptors,” Molecular and Cellular Biology, vol. 19, no. 2, pp. 1539–1546, 1999.
- D. G. Woodside, A. Obergfell, A. Talapatra, D. A. Calderwood, S. J. Shattil, and M. H. Ginsberg, “The N-terminal SH2 domains of Syk and ZAP-70 mediate phosphotyrosine-independent binding to integrin β cytoplasmic domains,” The Journal of Biological Chemistry, vol. 277, no. 42, pp. 39401–39408, 2002.
- Z. Jakus, S. Fodor, C. L. Abram, C. A. Lowell, and A. Mócsai, “Immunoreceptor-like signaling by β2 and β3 integrins,” Trends in Cell Biology, vol. 17, no. 10, pp. 493–501, 2007.
- D. Frommhold, I. Mannigel, J. Schymeinsky et al., “Spleen tyrosine kinase Syk is critical for sustained leukocyte adhesion during inflammation in vivo,” BMC Immunology, vol. 8, article 31, 2007.
- C. M. Vines, J. W. Potter, Y. Xu et al., “Inhibition of β2 integrin receptor and Syk kinase signaling in monocytes by the Src family kinase Fgr,” Immunity, vol. 15, no. 4, pp. 507–519, 2001.
- A. Mócsai, C. L. Abram, Z. Jakus, Y. Hu, L. L. Lanier, and C. A. Lowell, “Integrin signaling in neutrophils and macrophages uses adaptors containing immunoreceptor tyrosine-based activation motifs,” Nature Immunology, vol. 7, no. 12, pp. 1326–1333, 2006.
- A. Urzainqui, J. M. Serrador, F. Viedma et al., “ITAM-based interaction of ERM proteins with Syk mediates signaling by the leukocyte adhesion receptor PSGL-1,” Immunity, vol. 17, no. 4, pp. 401–412, 2002.
- A. Zarbock, C. A. Lowell, and K. Ley, “Spleen tyrosine kinase Syk is necessary for E-selectin-induced αLβ2 integrin-mediated rolling on intercellular adhesion molecule-1,” Immunity, vol. 26, no. 6, pp. 773–783, 2007.
- N. C. Rogers, E. C. Slack, A. D. Edwards et al., “Syk-dependent cytokine induction by dectin-1 reveals a novel pattern recognition pathway for C type lectins,” Immunity, vol. 22, no. 4, pp. 507–517, 2005.
- D. M. Underhill, E. Rossnagle, C. A. Lowell, and R. M. Simmons, “Dectin-1 activates Syk tyrosine kinase in a dynamic subset of macrophages for reactive oxygen production,” Blood, vol. 106, no. 7, pp. 2543–2550, 2005.
- O. Gross, H. Poeck, M. Bscheider et al., “Syk kinase signalling couples to the Nlrp3 inflammasome for anti-fungal host defence,” Nature, vol. 459, no. 7245, pp. 433–436, 2009.
- T. B. H. Geijtenbeek and S. I. Gringhuis, “Signalling through C-type lectin receptors: shaping immune responses,” Nature Reviews Immunology, vol. 9, no. 7, pp. 465–479, 2009.
- J. A. van Ziffle and C. A. Lowell, “Neutrophil-specific deletion of Syk kinase results in reduced host defense to bacterial infection,” Blood, vol. 114, no. 23, pp. 4871–4882, 2009.
- S.-T. Chen, Y.-L. Lin, M.-T. Huang et al., “CLEC5A is critical for dengue-virus-induced lethal disease,” Nature, vol. 453, no. 7195, pp. 672–676, 2008.
- S. Yamasaki, E. Ishikawa, M. Sakuma, H. Hara, K. Ogata, and T. Saito, “Mincle is an ITAM-coupled activating receptor that senses damaged cells,” Nature Immunology, vol. 9, no. 10, pp. 1179–1188, 2008.
- D. Sancho, O. P. Joffre, A. M. Keller et al., “Identification of a dendritic cell receptor that couples sensing of necrosis to immunity,” Nature, vol. 458, no. 7240, pp. 899–903, 2009.
- C. Huysamen, J. A. Willment, K. M. Dennehy, and G. D. Brown, “CLEC9A is a novel activation C-type lectin-like receptor expressed on BDCA3+ dendritic cells and a subset of monocytes,” The Journal of Biological Chemistry, vol. 283, no. 24, pp. 16693–16701, 2008.
- F. Colucci, E. Schweighoffer, E. Tomasello et al., “Natural cytotoxicity uncoupled from the Syk and ZAP-70 intracellular kinases,” Nature Immunology, vol. 3, no. 3, pp. 288–294, 2002.
- Y. S. Bae, J. H. Lee, S. H. Choi et al., “Macrophages generate reactive oxygen species in response to minimally oxidized low-density lipoprotein: toll-like receptor 4- and spleen tyrosine kinase-dependent activation of NADPH oxidase 2,” Circulation Research, vol. 104, no. 2, pp. 210–218, 2009.
- S.-H. Choi, R. Harkewicz, J. H. Lee et al., “Lipoprotein accumulation in macrophages via toll-like receptor-4-dependent fluid phase uptake,” Circulation Research, vol. 104, no. 12, pp. 1355–1363, 2009.
- J. Y. Yoon, H. Y. Jeong, S. H. Kim et al., “Methanol extract of Evodia lepta displays Syk/Src-targeted anti-inflammatory activity,” Journal of Ethnopharmacology, vol. 148, no. 3, pp. 999–1007, 2013.
- D. Jeong, W. S. Yang, Y. Yang et al., “In vitro and in vivo anti-inflammatory effect of Rhodomyrtus tomentosa methanol extract,” Journal of Ethnopharmacology, vol. 146, no. 1, pp. 205–213, 2013.
- W. S. Yang, J. Lee, T. W. Kim et al., “Src/NF-κB-targeted inhibition of LPS-induced macrophage activation and dextran sodium sulphate-induced colitis by Archidendron clypearia methanol extract,” Journal of Ethnopharmacology, vol. 142, no. 1, pp. 287–293, 2012.
- T. Yu, S. Lee, W. S. Yang et al., “The ability of an ethanol extract of Cinnamomum cassia to inhibit Src and spleen tyrosine kinase activity contributes to its anti-inflammatory action,” Journal of Ethnopharmacology, vol. 139, no. 2, pp. 566–573, 2012.
- Y. I. Miller, S.-H. Choi, P. Wiesner, and Y. S. Bae, “The SYK side of TLR4: signalling mechanisms in response to LPS and minimally oxidized LDL,” The British Journal of Pharmacology, vol. 167, no. 5, pp. 990–999, 2012.
- D. Jeong, Y. S. Yi, G. H. Sung et al., “Anti-inflammatory activities and mechanisms of Artemisia asiatica ethanol extract,” Journal of Ethnopharmacology, vol. 152, no. 3, pp. 87–496, 2014.
- H. Y. Jeong, G. H. Sung, J. H. Kim et al., “Syk and Src are major pharmacological targets of a Cerbera manghas methanol extract with kaempferol-based anti-inflammatory activity,” Journal of Ethnopharmacology, vol. 151, no. 2, pp. 960–969, 2014.
- Y. Yang, T. Yu, Y. G. Lee et al., “Methanol extract of Hopea odorata suppresses inflammatory responses via the direct inhibition of multiple kinases,” Journal of Ethnopharmacology, vol. 145, no. 2, pp. 598–607, 2013.
- W. S. Yang, D. Jeong, Y. S. Yi et al., “Myrsine seguinii ethanolic extract and its active component quercetin inhibit macrophage activation and peritonitis induced by LPS by targeting to Syk/Src/IRAK-1,” Journal of Ethnopharmacology, vol. 151, no. 3, pp. 1165–1174, 2014.
- W. S. Yang, D. Jeong, Y. S. Yi et al., “IRAK1/4-targeted anti-inflammatory action of caffeic acid,” Mediators of Inflammation, vol. 2013, Article ID 518183, 12 pages, 2013.
- M. Endale, S.-C. Park, S. Kim et al., “Quercetin disrupts tyrosine-phosphorylated phosphatidylinositol 3-kinase and myeloid differentiation factor-88 association, and inhibits MAPK/AP-1 and IKK/NF-κB-induced inflammatory mediators production in RAW 264.7 cells,” Immunobiology, vol. 218, no. 12, pp. 1452–1467, 2013.
- J. A. Hamerman, N. K. Tchao, C. A. Lowell, and L. L. Lanier, “Enhanced Toll-like receptor responses in the absence of signaling adaptor DAP12,” Nature Immunology, vol. 6, no. 6, pp. 579–586, 2005.
- M. Turner, P. J. Mee, P. S. Costello et al., “Perinatal lethality and blocked B-cell development in mice lacking the tyrosine kinase Syk,” Nature, vol. 378, no. 6554, pp. 298–302, 1995.
- M. Gururajan, T. Dasu, S. Shahidain et al., “Spleen tyrosine kinase (Syk), a novel target of curcumin, is required for B lymphoma growth,” Journal of Immunology, vol. 178, no. 1, pp. 111–121, 2007.
- K. Ashikawa, S. Majumdar, S. Banerjee, A. C. Bharti, S. Shishodia, and B. B. Aggarwal, “Piceatannol inhibits TNF-induced NF-κB activation and NF-κB-mediated gene expression through suppression of IκBα kinase and p65 phosphorylation,” Journal of Immunology, vol. 169, no. 11, pp. 6490–6497, 2002.
- P. Ruzza, B. Biondi, and A. Calderan, “Therapeutic prospect of Syk inhibitors,” Expert Opinion on Therapeutic Patents, vol. 19, no. 10, pp. 1361–1376, 2009.
- N. Yamamoto, K. Takeshita, M. Shichijo et al., “The orally available spleen tyrosine kinase inhibitor 2-[7-(3,4-dimethoxyphenyl)-imidazo[1,2-c]pyrimidin-5-ylamino]-nicotinamide dihydrochloride (BAY 61-3606) blocks antigen-induced airway inflammation in rodents,” Journal of Pharmacology and Experimental Therapeutics, vol. 306, no. 3, pp. 1174–1181, 2003.
- H. Hisamichi, R. Naito, A. Toyoshima et al., “Synthetic studies on novel Syk inhibitors. Part 1: synthesis and structure-activity relationships of pyrimidine-5-carboxamide derivatives,” Bioorganic & Medicinal Chemistry, vol. 13, no. 16, pp. 4936–4951, 2005.
- B. R. Wong, E. B. Grossbard, D. G. Payan, and E. S. Masuda, “Targeting Syk as a treatment for allergic and autoimmune disorders,” Expert Opinion on Investigational Drugs, vol. 13, no. 7, pp. 743–762, 2004.
- M. Bajpai, P. Chopra, S. G. Dastidar, and A. Ray, “Spleen tyrosine kinase: a novel target for therapeutic intervention of rheumatoid arthritis,” Expert Opinion on Investigational Drugs, vol. 17, no. 5, pp. 641–659, 2008.
- K. Blease, “Targeting kinases in asthma,” Expert Opinion on Investigational Drugs, vol. 14, no. 10, pp. 1213–1220, 2005.
- E. S. Masuda and J. Schmitz, “Syk inhibitors as treatment for allergic rhinitis,” Pulmonary Pharmacology & Therapeutics, vol. 21, no. 3, pp. 461–467, 2008.
- A. Podolanczuk, A. H. Lazarus, A. R. Crow, E. Grossbard, and J. B. Bussel, “Of mice and men: an open-label pilot study for treatment of immune thrombocytopenic purpura by an inhibitor of Syk,” Blood, vol. 113, no. 14, pp. 3154–3160, 2009.
- F. R. Bahjat, P. R. Pine, A. Reitsma et al., “An orally bioavailable spleen tyrosine kinase inhibitor delays disease progression and prolongs survival in murine lupus,” Arthritis and Rheumatism, vol. 58, no. 5, pp. 1433–1444, 2008.
- C. H. Chui, R. S. M. Wong, G. Y. M. Cheng et al., “Antiproliferative ability of a combination regimen of crocodile egg extract, wild radix ginseng and natural Ganoderma lucidum on acute myelogenous leukemia,” Oncology Reports, vol. 16, no. 6, pp. 1313–1316, 2006.
- P. R. Pine, B. Chang, N. Schoettler et al., “Inflammation and bone erosion are suppressed in models of rheumatoid arthritis following treatment with a novel Syk inhibitor,” Clinical Immunology, vol. 124, no. 3, pp. 244–257, 2007.
- G. Coffey, F. DeGuzman, M. Inagaki et al., “Specific inhibition of spleen tyrosine kinase suppresses leukocyte immune function and inflammation in animal models of rheumatoid arthritis,” Journal of Pharmacology and Experimental Therapeutics, vol. 340, no. 2, pp. 350–359, 2012.
- N. Ozaki, S. Suzuki, M. Ishida et al., “Syk-dependent signaling pathways in neutrophils and macrophages are indispensable in the pathogenesis of anti-collagen antibody-induced arthritis,” International Immunology, vol. 24, no. 9, pp. 539–550, 2012.
- Y.-S. Yi, W. Ayala-López, S. A. Kularatne, and P. S. Low, “Folate-targeted hapten immunotherapy of adjuvant-induced arthritis: comparison of hapten potencies,” Molecular Pharmaceutics, vol. 6, no. 4, pp. 1228–1236, 2009.
- M. E. Weinblatt, A. Kavanaugh, R. Burgos-Vargas et al., “Treatment of rheumatoid arthritis with a Syk kinase inhibitor: a twelve-week, randomized, placebo-controlled trial,” Arthritis and Rheumatism, vol. 58, no. 11, pp. 3309–3318, 2008.
- M. Kovarova and J. Rivera, “A molecular understanding of mast cell activation and the promise of anti-allergic therapeutics,” Current Medicinal Chemistry, vol. 11, no. 15, pp. 2083–2091, 2004.
- A. B. Rossi, E. Herlaar, S. Braselmann et al., “Identification of the Syk kinase inhibitor R112 by a human mast cell screen,” Journal of Allergy and Clinical Immunology, vol. 118, no. 3, pp. 749–755, 2006.
- E. O. Meltzer, R. B. Berkowitz, and E. B. Grossbard, “An intranasal Syk-kinase inhibitor (R112) improves the symptoms of seasonal allergic rhinitis in a park environment,” Journal of Allergy and Clinical Immunology, vol. 115, no. 4, pp. 791–796, 2005.
- O. N. Pamuk, P. H. Lapchak, P. Rani, P. Pine, J. J. Dalle Lucca, and G. C. Tsokos, “Spleen tyrosine kinase inhibition prevents tissue damage after ischemia-reperfusion,” The American Journal of Physiology—Gastrointestinal and Liver Physiology, vol. 299, no. 2, pp. G391–G399, 2010.
- P. H. Lapchak, L. Kannan, P. Rani et al., “Inhibition of Syk activity by R788 in platelets prevents remote lung tissue damage after mesenteric ischemia-reperfusion injury,” The American Journal of Physiology—Gastrointestinal and Liver Physiology, vol. 302, no. 12, pp. G1416–G1422, 2012.
- A. Rahman and D. A. Isenberg, “Systemic lupus erythematosus,” The New England Journal of Medicine, vol. 358, no. 9, pp. 929–939, 2008.
- J. Smith, J. P. McDaid, G. Bhangal et al., “A spleen tyrosine kinase inhibitor reduces the severity of established glomerulonephritis,” Journal of the American Society of Nephrology, vol. 21, no. 2, pp. 231–236, 2010.
- G.-M. Deng, L. Liu, F. R. Bahjat, P. R. Pine, and G. C. Tsokos, “Suppression of skin and kidney disease by inhibition of spleen tyrosine kinase in lupus-prone mice,” Arthritis and Rheumatism, vol. 62, no. 7, pp. 2086–2092, 2010.
- Y.-C. Lin, D.-Y. Huang, C.-L. Chu, and W.-W. Lin, “Anti-inflammatory actions of Syk inhibitors in macrophages involve non-specific inhibition of toll-like receptors-mediated JNK signaling pathway,” Molecular Immunology, vol. 47, no. 7-8, pp. 1569–1578, 2010.
- B. B. Au-Yeung, S. Deindl, L.-Y. Hsu et al., “The structure, regulation, and function of ZAP-70,” Immunological Reviews, vol. 228, no. 1, pp. 41–57, 2009.
- H. Wang, T. A. Kadlecek, B. B. Au-Yeung et al., “ZAP-70: an essential kinase in T-cell signaling,” Cold Spring Harbor Perspectives in Biology, vol. 2, no. 5, Article ID a002279, 2010.
- S. Kumar-Roiné, M. Matsui, K. Reybier et al., “Ability of certain plant extracts traditionally used to treat ciguatera fish poisoning to inhibit nitric oxide production in RAW 264.7 macrophages,” Journal of Ethnopharmacology, vol. 123, no. 3, pp. 369–377, 2009.
- A. M. Reddy, J. Y. Lee, J. H. Seo et al., “Artemisolide from Artemisia asiatica: nuclear factor-kappaB (NF-kappaB) inhibitor suppressing prostaglandin E2 and nitric oxide production in macrophages,” Archives of Pharmacal Research, vol. 29, no. 7, pp. 591–597, 2006.
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