THE INTERDEPENDENT MODULATION OF HYALURONAN SYNTHESIS BY TGF-BETA-1 AND EXTRACELLULAR-MATRIX - CONSEQUENCES FOR THE CONTROL OF CELL-MIGRATION

Authors
Citation
I. Ellis et Sl. Schor, THE INTERDEPENDENT MODULATION OF HYALURONAN SYNTHESIS BY TGF-BETA-1 AND EXTRACELLULAR-MATRIX - CONSEQUENCES FOR THE CONTROL OF CELL-MIGRATION, Growth factors, 12(3), 1995, pp. 211-222
Citations number
85
Categorie Soggetti
Biology
Journal title
ISSN journal
08977194
Volume
12
Issue
3
Year of publication
1995
Pages
211 - 222
Database
ISI
SICI code
0897-7194(1995)12:3<211:TIMOHS>2.0.ZU;2-L
Abstract
The principal objective of this communication has been to determine th e manner in which two tissue culture substrata (plastic dishes and typ e I collagen gels) modulate the response of adult skin fibroblasts to TGF-beta 1 with respect to hyaluronan (HA) synthesis. Our results indi cate that (a) fibroblasts cultured on collagen gels synthesised more H A compared to cells plated at the same density on plastic dishes, (b) this up-regulation in total HA synthesis by collagen-cultured cells wa s accompanied by an increase in the relative proportion of high molecu lar mass species of newly synthesised HA, and (c) the specific effect of TGF-beta 1 on HA synthesis was dependent upon the substratum: i.e. TGF-beta 1 inhibited HA synthesis by subconfluent fibroblasts cultured on both substrata, had no apparent effect on confluent cells cultured on collagen gels, and stimulated HA synthesis by confluent cells cult ured on plastic dishes. The TGF beta-stimuiation of HA synthesis by co nfluent fibroblasts cultured on plastic dishes persisted when these ce lls were transferred to collagen gels in the absence of further TGF-be ta 1; interestingly, a second exposure of these plastic pre-incubated cells to TGF-beta 1 whilst growing on collagen resulted in a down-regu lation in HA synthesis. Confluent fibroblasts pre-incubated with TGF-b eta 1 for 24 h on plastic dishes (i.e. under conditions which stimulat e HA synthesis) also displayed an HA-dependent stimulation in cell mig ration when subsequently plated onto collagen gels in the absence of f urther cytokine.