The synthetic peptide SVVYGLR promotes cell motility of myogenic cells and facilitates differentiation in skeletal muscle regeneration.
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M. Kogo | Hirofumi Yamamoto | Yuhki Yokoyama | N. Kawaguchi | S. Mori | Xin Wu | Susumu Tanaka | Yohei Fujishita | Takasuke Usuki
[1] H. Yatani,et al. Synthetic osteopontin-derived peptide SVVYGLR can induce neovascularization in artificial bone marrow scaffold biomaterials. , 2007, Dental materials journal.
[2] R. Farrar,et al. Controlled delivery of SDF-1α and IGF-1: CXCR4(+) cell recruitment and functional skeletal muscle recovery. , 2015, Biomaterials science.
[3] M. Hemler,et al. Role of Transmembrane 4 Superfamily (Tm4sf) Proteins Cd9 and Cd81 in Muscle Cell Fusion and Myotube Maintenance , 1999, The Journal of cell biology.
[4] U. Müller,et al. Beta1 integrins regulate myoblast fusion and sarcomere assembly. , 2003, Developmental cell.
[5] C. Rathbone,et al. Volumetric muscle loss leads to permanent disability following extremity trauma. , 2015, Journal of rehabilitation research and development.
[6] G. Vanderstraeten,et al. Treatment of Skeletal Muscle Injury: A Review , 2012, ISRN orthopedics.
[7] M. Kogo,et al. Osteopontin-derived synthetic peptide SVVYGLR has potent utility in the functional regeneration of oral and maxillofacial skeletal muscles , 2019, Peptides.
[8] B. Carlson,et al. MyoD and myogenin protein expression in skeletal muscles of senile rats , 2003, Cell and Tissue Research.
[9] Y. Tsao,et al. PEDF-derived peptide promotes skeletal muscle regeneration through its mitogenic effect on muscle progenitor cells. , 2015, American journal of physiology. Cell physiology.
[10] M. Sampaolesi,et al. Cell therapy strategies and improvements for muscular dystrophy , 2010, Cell Death and Differentiation.
[11] K. Uaesoontrachoon,et al. Osteopontin and skeletal muscle myoblasts: association with muscle regeneration and regulation of myoblast function in vitro. , 2008, The international journal of biochemistry & cell biology.
[12] A. Uchinaka,et al. Evaluation of dermal wound healing activity of synthetic peptide SVVYGLR. , 2017, Biochemical and biophysical research communications.
[13] A. Uchinaka,et al. Improvement of cardiac function after implanting the osteopontin-derived peptide SVVYGLR in a hamster model of dilated cardiomyopathy. , 2015, Interactive cardiovascular and thoracic surgery.
[14] Jeff W Lichtman,et al. Functional muscle regeneration with combined delivery of angiogenesis and myogenesis factors , 2009, Proceedings of the National Academy of Sciences.
[15] C. Pagel,et al. Osteopontin, inflammation and myogenesis: influencing regeneration, fibrosis and size of skeletal muscle , 2013, Journal of Cell Communication and Signaling.
[16] N. Adachi,et al. Acceleration of muscle regeneration by local injection of muscle-specific microRNAs in rat skeletal muscle injury model , 2009, Journal of cellular and molecular medicine.
[17] K. Myburgh,et al. In vitro myoblast motility models: investigating migration dynamics for the study of skeletal muscle repair , 2013, Journal of Muscle Research and Cell Motility.
[18] A. Uchinaka,et al. Overexpression of collagen type III in injured myocardium prevents cardiac systolic dysfunction by changing the balance of collagen distribution , 2018, The Journal of thoracic and cardiovascular surgery.
[19] M. Sandri,et al. Mechanisms regulating skeletal muscle growth and atrophy , 2013, The FEBS journal.
[20] P. Lønning,et al. Long-term cultures of bone marrow-derived human mesenchymal stem cells frequently undergo spontaneous malignant transformation. , 2009, Cancer research.
[21] D. Sassoon,et al. Stem cells in the hood: the skeletal muscle niche. , 2012, Trends in molecular medicine.
[22] A. Uchinaka,et al. Transplantation of myoblast sheets that secrete the novel peptide SVVYGLR improves cardiac function in failing hearts. , 2013, Cardiovascular research.
[23] M. Matsuo,et al. Angiogenic activity of osteopontin-derived peptide SVVYGLR. , 2003, Biochemical and biophysical research communications.
[24] M. Rudnicki,et al. Determination versus differentiation and the MyoD family of transcription factors. , 1995, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[25] C. Sen,et al. miRNA control of tissue repair and regeneration. , 2015, The American journal of pathology.
[26] Adeline Koh,et al. Osteopontin Expression Is Required for Myofibroblast Differentiation , 2008, Circulation research.
[27] W. Benedict,et al. Pigment epithelium-derived factor: a potent inhibitor of angiogenesis. , 1999, Science.
[28] A. Uchinaka,et al. SVVYGLR motif of the thrombin-cleaved N-terminal osteopontin fragment enhances the synthesis of collagen type III in myocardial fibrosis , 2015, Molecular and Cellular Biochemistry.
[29] J. Chen,et al. Differential effects of the integrins alpha9beta1, alphavbeta3, and alphavbeta6 on cell proliferative responses to tenascin. Roles of the beta subunit extracellular and cytoplasmic domains. , 1996, The Journal of biological chemistry.
[30] A. Schilling,et al. Current Methods for Skeletal Muscle Tissue Repair and Regeneration , 2018, BioMed research international.