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INDUCTION OF CELLULAR PROCESSES CONTAINING COLLAGENASE AND RETINOID BY INTEGRIN‐BINDING TO INTERSTITIAL COLLAGEN IN HEPATIC STELLATE CELL CULTURE
Author(s) -
SATO MITSURU,
KOJIMA NAOSUKE,
MIURA MITSUTAKA,
IMAI KATSUYUKI,
SENOO HARUKI
Publication year - 1998
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1006/cbir.1998.0234
Subject(s) - hepatic stellate cell , microbiology and biotechnology , integrin , chemistry , fibronectin , type i collagen , collagen, type i, alpha 1 , collagenase , biochemistry , biophysics , extracellular matrix , biology , cell , enzyme , endocrinology
Cultered hepatic stellate cells were induced to elongate long, multipolar cellular processes by interstitial collagen gel used as a substratum, as compared to flattened or round cell shapes on polystyrene surface or on Matrigel containing the basement membrane components, respectively. The process induction was inhibited by several reagents as follows: (1) anti‐integrin α2 antibody; (2) an oligopeptide, DGEA, an integrin‐binding sequence in type I collagen molecule; (3) wortmannin, a phosphatidylinositol 3‐kinase inhibitor. Protein tyrosine phosphorylation was enhanced throughout cells including cellular processes by culturing on type I collagen gel. Dual fluorescence staining showed that the core of the processes contained microtubules, whereas the periphery of the processes comprised fibrillar actin. Thus, the process extension was found to depend on integrin‐binding to type I collagen fibres, followed by signal transduction and cytoskeleton assembly. The cellular processes included interstitial collagenase and vitamin A‐containing lipid droplets. The lipid droplets and vitamin A‐autofluorescence were increased by retinyl acetate addition to the culture medium, suggesting an important role of processes in hepatic stellate cell function.