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Publication : The novel cytokine p43 stimulates dermal fibroblast proliferation and wound repair.

First Author  Park SG Year  2005
Journal  Am J Pathol Volume  166
Issue  2 Pages  387-98
PubMed ID  15681823 Mgi Jnum  J:95974
Mgi Id  MGI:3528513 Doi  10.1016/S0002-9440(10)62262-6
Citation  Park SG, et al. (2005) The novel cytokine p43 stimulates dermal fibroblast proliferation and wound repair. Am J Pathol 166(2):387-98
abstractText  The multifunctional cytokine p43 acts on endothelial and immune cells to control angiogenesis and inflammation. In this report, we describe an additional activity of p43 that specifically promotes fibroblast proliferation and wound repair. In skin wound regions from mice, tumor necrosis factor-alpha induced p43 expression and secretion from macrophages recruited to the site. p43 also promoted fibroblast proliferation through its 146-amino acid N-terminal domain as revealed by deletion mapping. This p43-induced fibroblast proliferation was mediated by extracellular signal-regulated kinase (Erk). Depletion of endogenous p43 in mice by gene disruption retarded wound repair, whereas exogenous supplementation of recombinant human p43 to the wound area stimulated dermal fibroblast proliferation, collagen production, and wound closure. Thus, we have identified a novel p43 activity involving the stimulation of fibroblast proliferation, which could be applied therapeutically to aid wound repair.
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