Abstract
Expression of mRNA encoding sterol regulatory element binding protein (SREBP) isoforms (SREBP-1a, -1c, -2) and seven SREBP target genes decreased dramatically as a result of isolation and subsequent culture of primary rat hepatocytes. In standard maintenance medium (MM) expression remained low but when cultured in HepatoZYME (HZM), there was a selective increase in mRNA encoding SREBP-2 and a subset of SREBP target genes, a group characterised by promoters containing adjacent sterol regulatory element and nuclear factor Y (NF-Y) binding sequences. Quantification of all three NF-Y transcripts showed that expression of nuclear factor Y α subunit and nuclear factor Y β subunit mRNA increased during culture in HZM (in contrast to the situation with MM) whilst specificity protein 1, liver-x-receptor and hepatocyte nuclear factor-4α mRNA exhibited equivalent decreased expression in both HZM and MM. Our data indicate that HZM exerts a selective preservation of hepatocyte phenotype through actions on NF-Y expression directly or via an effect secondary to actions on SREBP-2 expression. These data add to the molecular dissection of the causes of hepatocyte dedifferentiation during culture and address means to develop approaches to prevent/limit phenotype change. © 2010 The Society for In Vitro Biology.
Original language | English |
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Pages (from-to) | 657-663 |
Number of pages | 6 |
Journal | In Vitro Cellular and Developmental Biology - Animal |
Volume | 46 |
Issue number | 8 |
DOIs | |
Publication status | Published - Sept 2010 |
Keywords
- HepatoZYME
- HMGCoA reductase
- LXR
- NF-Y
- Sp1