Types I and IV Procollagen Gene Expression in Cultured Rat Hepatocytes

Abstract

The molecular mechanism involved in the expression of collagens by hepatocytes wereinvestigated in both pure and co-culture with another rat liver epithelial cell type (RLEC). We measured the steady-state levels of mRNAs coding for proαl(I) and proαl (IV) chains by Northern analysis and by dot blotting, using specific recombinant cDNA probes. In freshly isolated hepatocytes, only small amounts of proαl (I) and proαl (IV) mRNAs were detected by dot-blot analysis. After 3 days in culture, the proαl (I) and proαl (IV) mRNA levels increased 2 to 5 times. The amount of proαl (IV) mRNAs was identical in hepatocyte cultured with RLECs while the proαl (I) mRNA level was 5 times that in pure hepatocyte culture. Hydrocortisone reduced proαl (I) mRNA in hepatocyte cultures, but had no effect on co-cultured cells. In both culture systems, this glucocorticoid did not act on the steady-state proαl (IV) mRNA level. Whatever the age and the type of culture (pure or mixed) RLECs exhibited the highest levels of proα1(I) and proα1(IV) mRNAs, which were reduced by hydrocortisone. These results show that procollagen gene expression by hepatocytes is not directly correlated with their functional state and that corticosteroids differently affect the expression of different collagen genes and collagen deposition.