Hepatocyte growth factor and Madin-Darby canine kidney cells: In vitro models of epithelial cell movement and morphogenesis

Authors
Citation
Df. Balkovetz, Hepatocyte growth factor and Madin-Darby canine kidney cells: In vitro models of epithelial cell movement and morphogenesis, MICROSC RES, 43(5), 1998, pp. 456-463
Citations number
64
Categorie Soggetti
Multidisciplinary
Journal title
MICROSCOPY RESEARCH AND TECHNIQUE
ISSN journal
1059910X → ACNP
Volume
43
Issue
5
Year of publication
1998
Pages
456 - 463
Database
ISI
SICI code
1059-910X(199812)43:5<456:HGFAMC>2.0.ZU;2-N
Abstract
It is becoming increasingly apparent that epithelial cell movement and chan ges in morphology are central to both development and regeneration of epith elial organs and are involved with pathological processes such as transform ation of epithelia to carcinoma and metastasis. Hepatocyte growth factor (H GF) is a mesenchymally derived growth factor with pleiotrophic effects on e pithelia depending on culture conditions. In vivo, HGF plays a role in mese nchymal-epithelial interactions. Madin-Darby canine kidney (MDCK) cells, wh ich share many properties with polarized epithelia in vivo, are remarkably sensitive to HGF. In vitro models of HGF-treated MDCK cells have proven to be useful for the study of epithelial cell movement and changes in morpholo gy. When cultured on plastic at low density, MDCK cells scatter in response to HGF. MDCK cells grown as cell suspensions in collagen gels form complex branching tubular structures in response to HGF. When cultivated as a mono layer on permeant supports, MDCK cells are well polarized with established E-cadherin mediated cell-cell junctions and dedifferentiate in response to HGF. Some of the mechanisms responsible for changes in cell movement and mo rphology that have been characterized using these models are summarized in this review Models of MDCK cells exposed to HGF will continue to be useful in the study of epithelial cell movement and morphogenesis in vitro and wil l provide important clues into the cellular mechanisms important during in vivo epithelial processes such as organ development, regeneration, and tran sformation to carcinoma. Published 1998 Wiley-Liss, Inc.