The effects of macrophage-stimulating protein on the migration, proliferation, and collagen synthesis of skin fibroblasts in vitro and in vivo

Tissue Engineering - Part A

Volumn 21, Issue 5-6, 2015, Pages 982-991

  Zhao, Jiajia ^a   Hu, Li ^a   Gong, Niya ^a   Tang, Qingming ^a   Du, Luyang ^a   Chen, Lili ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CELL CULTURE; COLLAGEN; ENZYME INHIBITION; FIBROBLASTS; MACROPHAGES; POLYMERASE CHAIN REACTION; PROTEINS; STEM CELLS; SYNTHESIS (CHEMICAL); TISSUE;

ADIPOSE DERIVED STEM CELLS; BACTERIAL CELLULOSE MEMBRANES; CONDITIONED MEDIUM; DERMAL FIBROBLASTS; INFLAMMATORY MEDIATORS; MATRIX METALLOPROTEINASE-1; OPTIMAL CONCENTRATION; REAL TIME POLYMERASE CHAIN REACTIONS;

BIOSYNTHESIS;

BACTERIAL POLYSACCHARIDE; CELLULOSE; COLLAGEN; COLLAGEN TYPE 1; COLLAGEN TYPE 3; INTERSTITIAL COLLAGENASE; MACROPHAGE ACTIVATING FACTOR; MACROPHAGE STIMULATION 1 RECEPTOR; MESSENGER RNA; UNCLASSIFIED DRUG; VIMENTIN; MACROPHAGE STIMULATING PROTEIN; MMP1 PROTEIN, HUMAN; ONCOPROTEIN; PROTEIN TYROSINE KINASE; RON PROTEIN; SCATTER FACTOR;

ANIMAL MODEL; ARTICLE; CELL COUNTING; CELL LEVEL; CELL MIGRATION; CELL PROLIFERATION; COLLAGEN SYNTHESIS; CONTROLLED STUDY; CYTOTOXICITY; HUMAN; HUMAN CELL; IMMUNOHISTOCHEMISTRY; IN VITRO STUDY; IN VIVO STUDY; KERATINOCYTE; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN CONTENT; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN SECRETION; REAL TIME POLYMERASE CHAIN REACTION; SKIN FIBROBLAST; SKIN INJURY; UPREGULATION; WOUND CLOSURE; WOUND HEALING; ADOLESCENT; ADULT; ANIMAL; BAGG ALBINO MOUSE; BIOSYNTHESIS; CELL MOTION; CELL SHAPE; CYTOLOGY; DRUG EFFECTS; FIBROBLAST; GENETICS; METABOLISM; SKIN; YOUNG ADULT;

BACTERIA (MICROORGANISMS);

ADOLESCENT; ADULT; ANIMALS; CELL MOVEMENT; CELL PROLIFERATION; CELL SHAPE; COLLAGEN; FIBROBLASTS; HEPATOCYTE GROWTH FACTOR; HUMANS; IMMUNOHISTOCHEMISTRY; KERATINOCYTES; MALE; MATRIX METALLOPROTEINASE 1; MICE, INBRED BALB C; PROTO-ONCOGENE PROTEINS; REAL-TIME POLYMERASE CHAIN REACTION; RECEPTOR PROTEIN-TYROSINE KINASES; SKIN; VIMENTIN; WOUND HEALING; YOUNG ADULT;

EID: 84924417083     PISSN: 19373341     EISSN: 1937335X     Source Type: Journal    
DOI: 10.1089/ten.tea.2013.0726     Document Type: Article

References (43)

1. The natural healing process of skin wounds. Prescrire Int 22, 95, 2013.
2. Reinke, J.M., and Sorg, H. Wound repair and regeneration. Eur Surg Res 49, 35, 2012.
3. Stella, M.C., Vercelli, A., Repici, M., Follenzi, A., and Comoglio, P.M. Macrophage stimulating protein is a novel neurotrophic factor. Mol Biol Cell 12, 1341, 2001.
4. McElwee, K.J., Huth, A., Kissling, S., and Hoffmann, R. Macrophage-stimulating protein promotes hair growth ex vivo and induces anagen from telogen stage hair follicles in vivo. J Invest Dermatol 123, 34, 2004.
5. Tong, X.M., Wang, J.C., Shen, Y., Xie, J.J., Zhang, J.Y., and Jin, J. Inhibition of inflammatory mediators and related signaling pathways by macrophage-stimulating protein in rheumatoid arthritis synovial fibroblasts. Inflamm Res 60, 823, 2011.
6. Wang, M.H., Dlugosz, A.A., Sun, Y., Suda, T., Skeel, A., and Leonard, E.J. Macrophage-stimulating protein induces proliferation and migration of murine keratinocytes. Exp Cell Res 10, 226, 1996.
7. Medico, E., Mongiovi, A.M., Huff, J., Jelinek, M.A., Follenzi, A., Gaudino, G., et al. The tyrosine kinase receptors Ron and Sea control "'scattering" and morphogenesis of liver progenitor cells in vitro. Mol Biol Cell 7, 495, 1996.
8. Danilkovitch, A., Donley, S., Skeel, A., and Leonard, E.J. Two independent signaling pathways mediate the antiapoptotic action of macrophage-stimulating protein on epithelial cells. Mol Cell Biol 20, 2218, 2000.
9. Danilkovitch-Miagkova, A., and Leonard, E.J. Antiapoptotic action of macrophage stimulating protein (MSP). Apoptosis 6, 183, 2001.
10. Kurihara, N., Iwama, A., Tatsumi, J., Ikeda, K., and Suda, T. Macrophage-stimulating protein activates STK receptor tyrosine kinase on osteoclasts and facilitates, bone resorption by osteoclast-like cells. Blood 87, 3704, 1996.
11. Kretschmann, K.L., Eyob, H., Buys, S.S., and Welm A.L. The macrophage stimulating protein/Ron pathway as a potential therapeutic target to impede multiple mechanisms involved in breast cancer progression. Curr Drug Targets 11, 1157, 2010.
12. Gaudino, G., Avantaggiato, V., Follenzi, A., Acampora, D., Simeone, A., and Comoglio, P.M. The protooncogene RON is involved in development of epithelial, boneandneuro-endocrine tissues. Oncogene 11, 2627, 1995.
13. Wang, M.H., Zhou, Y.Q., and Chen, Y.Q. Macrophagestimulating protein and RON receptor tyrosine kinase: potential regulators of macrophage inflammatory activities. Scand J Immunol 56, 545, 2002.
14. Nanney, L.B., Skeel, A., Luan, J., Polis, S., Richmond, A., Wang, M.H., and Leonard E.J. Proteolytic cleavage and activation of pro-macrophage-stimulating protein and upregulation of its receptor in tissue injury. J Invest Dermatol 111, 573, 1998.
15. Cowin, A.J., Kallincos, N., Hatzirodos, N., Robertson, J.G., Pickering, K.J., Couper, J., and Belford, D.A. Hepatocyte growth factor and macrophage-stimulating protein are upregulated during excisional wound repair in rats. Cell Tissue Res 306, 239, 2001.
16. Huang, S.P., Hsu, C.C., Chang, S.C., Wang, C.H., Deng, S.C., Dai, N.T., et al. Adipose-derived stem cells seeded on acellular dermal matrix grafts enhance wound healing in a murine model of a full-thickness defect. Ann Plast Surg 69, 656, 2012.
17. Cherubino, M., Rubin, J.P., Miljkovic, N., Kelmendi-Doko, A., and Marra K.G. Adipose-derived stem cells for wound healing applications. Ann Plast Surg 66, 210, 2011.
18. Jeong, J.H. Adipose stem cells and skin repair. Curr Stem Cell Res Ther 5, 137, 2010.
19. Liu, S., Zhang, H., Zhang, X., Lu, W., Huang, X., Xie, H., et al. Synergistic angiogenesis promoting effects of extracellular matrix scaffolds and adipose-derived stem cells during wound repair. Tissue Eng Part A 17, 725, 2011.
20. Maxson, S., Lopez, E.A., Yoo, D., Danilkovitch-Miagkova, A., and Leroux, M.A. Concise review: role of mesenchymal stem cells in wound repair. Stem Cells Transl Med 1, 142, 2012.
21. Hu, L., Zhao, J., Liu, J., Gong, N., and Chen, L. Effects of adipose stem cell-conditioned medium on the migration of vascular endothelial cells, fibroblasts and keratinocytes. Exp Ther Med 5, 701, 2013.
22. Hu, L., Hu, J., Zhao, J., Liu, J., Ouyang, W., Yang, C., et al. Side-by-side comparison of the biological characteristics of human umbilical cord and adipose tissuederived mesenchymal stem cells. Biomed Res Int 2013, 438243, 2013.
23. Daimon, E., Shibukawa, Y., and Wada, Y. Calponin 3 regulates stress fiber formation in dermal fibroblasts during wound healing. Arch Dermatol Res 305, 571, 2013.
24. Hakkinen, L., Koivisto, L., and Larjava, H. An improved method for culture of epidermal keratinocytes from newborn mouse skin. Methods Cell Sci 23, 189, 2001.
25. Wang, Y., Xu, M., Dong, H., Liu, Y., Zhao, P., Niu, W., et al. Effects of PerClot-on the healing of full-thickness skin wounds in rats. Acta Histochem 114, 311, 2012.
26. Adamskaya, N., Dungel, P., Mittermayr, R., Hartinger, J., Feichtinger, G., Wassermann, K., et al. Light therapy by blue LED improves wound healing in an excision model in rats. Injury 42, 917, 2011.
27. Gauglitz, G.G., and Jeschke, M.G. Combined gene and stem cell therapy for cutaneouswound healing. Mol Pharm 8, 1471, 2011.
28. Lee, S.H., Jin, S.Y., Song, J.S., Seo, K.K., and Cho, K.H. Paracrine effects of adipose-derived stem cells on keratinocytes and dermal fibroblasts. Ann Dermatol 24, 136, 2012.
29. Kim, W.S., Park, B.S., Sung, J.H., Yang, J.M., Park, S.B., Kwak, S.J., and Park, J.S. Wound healing effect of adipose-derived stem cells: a critical role of secretory factors on human dermal fibroblasts. J Dermatol Sci 48, 15, 2007.
30. Lee, S.H., Lee, J.H., and Cho, K.H. Effects of human adipose-derived stem cells on cutaneous wound healing in nude mice. Ann Dermatol 23, 150, 2011.
31. Feres, K.J., Ischenko, I., and Hayman, M.J. The RON receptor tyrosine kinase promotes MSP-independent cell spreading and survival in breast epithelial cells. Oncogene 28, 279, 2009.
32. Gelbmann, C.M., Leeb, S.N., Vogl, D., Maendel, M., Herfarth, H., Schölmerich, J., et al. Inducible CD40 expression mediates NFkB activation and cytokine secretion in human colonic fibroblasts. Gut 52, 1448, 2003.
33. Santoro, M.M., Gaudino, G., and Marchisio, P.C. The MSP receptor regulates alpha6beta4 and alpha3beta1 integrins via 14-3-3 proteins in keratinocyte migration. Dev Cell 5, 257, 2003.
34. Van den Borne, S.W., Diez, J., Blankesteijn, W.M., Verjans, J., Hofstra, L., and Narula, J. Myocardial remodeling after infarction: the role of myofibroblasts. Nat Rev Cardiol 7, 30, 2010.
35. Grinnell, F., and Petroll, W.M. Cell motility and mechanics in three-dimensional collagen matrices. Annu Rev Cell Dev Biol 26, 335, 2010.
36. Martin, P. Wound healing-aiming for perfect skin regeneration. Science 276, 75, 1997.
37. Singer, A.J., and Clark, R.A. Cutaneous wound healing. N Engl J Med 341, 738, 1999.
38. Takayama, Y., and Aoki, R. Roles of lactoferrin on skin wound healing. Biochem Cell Biol 90, 497, 2012.
39. Martins V.L., Caley M., and O'Toole, E.A. Matrix metalloproteinases and epidermal wound repair. Cell Tissue Res 351, 255, 2013.
40. Chen, P., and Parks, W.C. Role of matrix metalloproteinases in epithelial migration. J Cell Biochem 108, 1233, 2009.
41. Overall, C.M., and López-Otń, C. Strategies for MMP inhibition in cancer: innovations for the post-trial era. Nat Rev Cancer 2, 657, 2002.
42. Mauviel, A., and Uitto, J. The extracellular-matrix in wound-healing-role of the cytokine network. Wounds 5, 137, 1993.
43. Juncker-Jensen, A., and Lund, L.R. Phenotypic overlap between MMP-13 and the plasminogen activation system during wound healing in mice. PLoS One 4, e16954, 2011.