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Division of Pediatric Gastroenterology and Nutrition, Department of Pediatrics, Vanderbilt University, Nashville, Tennessee 37232-2576
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-
1. 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.
cellular migration; tyrosine kinase; proliferation; extracellular matrix
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