Fibronectin blocks p38 and jnk activation by cyclic strain in Caco-2 cells

被引:10
作者
Zhang, JH
Li, W
Sumpio, BE
Basson, MD
机构
[1] John D Dingell Vet Adm Hosp Chief, VAMC, Dept Surg, Surg Serv 112, Detroit, MI 48201 USA
[2] Wayne State Univ, Detroit, MI 48202 USA
[3] Yale Univ, New Haven, CT 06520 USA
关键词
collagen; deformation; epithelium; fibronectin; intestine; MAPK; matrix; mucosa; signaling;
D O I
10.1016/S0006-291X(03)01044-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diverse repetitive forces deform the intestinal epithelium and basement membrane. Such repetitive deformation induces intestinal epithelial proliferation, differentiation, and intracellular signaling. Although at least some deformation-induced signals probably involve integrins, the matrix-dependence of these signals is poorly understood. We compared rapid strain activation of p38 and jnk in human Caco-2 intestinal epithelial cells cultured on collagen I, collagen IV, laminin, and tissue fibronectin. These signals were inhibited in cells on a fibronectin substrate, but activated by strain on collagens and laminin. Furthermore, adding 300 mug/ml plasma fibronectin (approximately the concentration found in plasma) to the culture medium inhibited strain activation of p38 and jnk in cells cultured on collagen. Since tissue and plasma fibronectin levels vary in acute or chronic inflammatory or infectious conditions, these results suggest that tissue or plasma fibronectin may modulate the intestinal epithelial response to repetitive deformation. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:746 / 749
页数:4
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