作者: Maroesjka Spiekman , Ewa Przybyt , Josée A. Plantinga , Susan Gibbs , Berend van der Lei
DOI: 10.1097/PRS.0000000000000504
关键词: Keloid 、 Pathology 、 Stromal cell 、 Cell biology 、 Paracrine signalling 、 Cellular differentiation 、 Myofibroblast contraction 、 Medicine 、 Adipose tissue 、 Wound healing 、 Extracellular matrix
摘要: Background: Adipose tissue-derived stromal cells augment wound healing and skin regeneration. It is unknown whether how they can also influence dermal scarring. The authors hypothesized that adipose inhibit adverse differentiation of fibroblasts induced by the pivotal factor in scarring, namely, transforming growth (TGF)-beta. Methods: TGF-beta 1-treated adult human keloid scar-derived were incubated with cell-conditioned medium assessed for proliferation differentiation, particularly production collagen, expression SM22 alpha, development hypertrophy contractility. Results: 1-induced was abolished medium. Simultaneously, reduced SM22a gene protein TGF beta fibroblasts, their contractility also. Furthermore, strongly transcription collagen I III genes corresponding proteins. In contrast, it tipped balance matrix turnover to degradation through stimulating metalloproteinase (MMP)-1, MMP-2, MMP-14, whereas MMP-2 activity up-regulated Even end-stage myofibroblasts (i.e., fibroblasts), suppressed myofibroblast contraction expression. Conclusion: show function a paracrine fashion.