Epidermal and hepatocyte growth factors stimulate chemotaxis in an intestinal epithelial cell line

被引:24
作者
Polk, DB [1 ]
Tong, W [1 ]
机构
[1] Vanderbilt Univ, Dept Pediat, Div Pediat Gastroenterol & Nutr, Nashville, TN 37232 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 277卷 / 06期
关键词
cellular migration; tyrosine kinase; proliferation; extracellular matrix;
D O I
10.1152/ajpcell.1999.277.6.C1149
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The migration of intestinal cells is important in the development and maintenance of normal epithelium, in a process that may be regulated by growth factors and cytokines. Although a number of growth factor receptors are expressed by intestinal cells, little progress has been made toward assignment of functional roles for these ligand-receptor systems. This study compares several growth factors and cytokines for their chemoattraction of the mouse small intestinal epithelial cell. line. Epidermal and hepatocyte growth factors stimulated a rapid 30-fold chemotaxis of cells with delayed threefold migration toward transforming growth factor-pi. Despite stimulating proliferation, keratinocyte, fibroblast, or insulin-like growth factors did not stimulate directed migration. Chemotaxis required tyrosine kinase and phosphatidylinositol phospholipase C activities but not protein kinase C or mitogen-activated protein kinase activity. These findings suggest that the repertoire of growth factors capable of regulating directed intestinal epithelial cell migration is limited and that a divergence exists in the signal transduction pathways for directed vs, nondirected migration.
引用
收藏
页码:C1149 / C1159
页数:11
相关论文
共 77 条
[1]   Platelet-derived growth factor and fibronectin-stimulated migration are differentially regulated by the Rac and extracellular signal-regulated kinase pathways [J].
Anand-Apte, B ;
Zetter, BR ;
Viswanathan, A ;
Qiu, RG ;
Chen, J ;
Ruggieri, R ;
Symons, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (49) :30688-30692
[2]   PRODUCTION OF TRANSFORMING GROWTH FACTOR-ALPHA BY NORMAL RAT SMALL-INTESTINE [J].
BARNARD, JA ;
POLK, WH ;
MOSES, HL ;
COFFEY, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (06) :C994-C1000
[3]   REGULATION OF INTESTINAL EPITHELIAL-CELL GROWTH BY TRANSFORMING GROWTH-FACTOR TYPE-BETA [J].
BARNARD, JA ;
BEAUCHAMP, RD ;
COFFEY, RJ ;
MOSES, HL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (05) :1578-1582
[4]   HUMAN ENTEROCYTE (CACO-2) MIGRATION IS MODULATED INVITRO BY EXTRACELLULAR-MATRIX COMPOSITION AND EPIDERMAL GROWTH-FACTOR [J].
BASSON, MD ;
MODLIN, IM ;
MADRI, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (01) :15-23
[5]  
BASSON MD, 1992, SURGERY, V112, P299
[6]   RECIPROCAL EXPRESSION OF LAMININ A-CHAIN ISOFORMS ALONG THE CRYPT-VILLUS AXIS IN THE HUMAN SMALL-INTESTINE [J].
BEAULIEU, JF ;
VACHON, PH .
GASTROENTEROLOGY, 1994, 106 (04) :829-839
[7]   EPIDERMAL GROWTH-FACTOR PROMOTES THE CHEMOTACTIC MIGRATION OF CULTURED RAT INTESTINAL EPITHELIAL-CELLS [J].
BLAY, J ;
BROWN, KD .
JOURNAL OF CELLULAR PHYSIOLOGY, 1985, 124 (01) :107-112
[9]   TYPE-I RECEPTORS SPECIFY GROWTH-INHIBITORY AND TRANSCRIPTIONAL RESPONSES TO TRANSFORMING GROWTH-FACTOR-BETA AND ACTIVIN [J].
CARCAMO, J ;
WEIS, FMB ;
VENTURA, F ;
WIESER, R ;
WRANA, JL ;
ATTISANO, L ;
MASSAGUE, J .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (06) :3810-3821
[10]   EPIDERMAL GROWTH-FACTOR RECEPTOR-MEDIATED CELL MOTILITY - PHOSPHOLIPASE-C ACTIVITY IS REQUIRED, BUT MITOGEN-ACTIVATED PROTEIN-KINASE ACTIVITY IS NOT SUFFICIENT FOR INDUCED CELL-MOVEMENT [J].
CHEN, P ;
XIE, H ;
SEKAR, MC ;
GUPTA, K ;
WELLS, A .
JOURNAL OF CELL BIOLOGY, 1994, 127 (03) :847-857