Keratinocyte growth factor promotes cell motility during alveolar epithelial repair in vitro

被引:62
作者
Galiacy, S
Planus, E
Lepetit, H
Féréol, S
Laurent, V
Ware, L
Isabey, D
Matthay, M
Harf, A
d'Orto, MP
机构
[1] Fac Med, INSERM, Unite U492, F-94010 Creteil, France
[2] Univ Paris 12, Fac Sci, F-94010 Creteil, France
[3] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[4] Hop Henri Mondor, Serv Physiol Explorat Fonctionnelles, F-94010 Creteil, France
关键词
KGF; migration; adhesion; fibronectin; epithelial; repair;
D O I
10.1016/S0014-4827(02)00049-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Epithelia play a key role as protective barriers, and mechanisms of repair are crucial for restoring epithelial barrier integrity, especially in the lung. Cell spreading and migration are the first steps of reepithelialization. Keratinocyte growth factor (KGF) plays a key role in lung epithelial repair and protects against various injuries. We hypothesized that KGF may protect the lung not only by inducing proliferation but also by promoting epithelial repair via enhanced epithelial cell migration. In an in vitro wound-healing model, we found that KGF enhanced wound closure by 33%. KGF acted primarily by inducing lamellipodia emission (73.2+/-3.9% of KGF-treated cells had lamellipodia vs 61.3+/-3.4% of control cells) and increasing their relative surface area (59+/-2.7% with KGF vs 48+/-2.0% in controls). KGF reduced cytoskeleton stiffness as measured by magnetic twisting cytometry and increased cell motility (5.8+/-0.42 mum/h with KGF vs 3.7+/-0.41 mum/h in controls). KGF-increased cell motility was associated with increased fibronectin deposition during wound closure and with fibronectin reorganization into fibrils at the rear of the cells. Taken together, our findings strongly suggest that KGF may promote epithelial repair through several mechanisms involved in cell migration. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:215 / 229
页数:15
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