Abstract:
:Rat pancreatic acinar cells AR 4-2J respond to dexamethasone by differentiation and a decreased proliferation rate. Protein labelling by [3H]-mevalonolactone, used as a precursor of farnesyl and geranylgeranyl isoprenoid groups, was increased in the presence of dexamethasone. In these same conditions, dexamethasone decreased HMG-CoA reductase activity, leading to a diminished isotopic dilution of the mevalonate precursor. As ras proteins, known to be involved in the regulation of proliferation and differentiation, need to be farnesylated for full biological function, we also measured the level of farnesyl transferase activity and found a dose-dependent decrease in dexamethasone treated cells. Despite these negative effects of dexamethasone on mevalonate pathway, there was no appearance of non-isoprenylated forms of ras, indicating that the level of isoprenoid precursors and farnesyl transferase activity were not limiting in this model.
journal_name
Mol Cell Biochemjournal_title
Molecular and cellular biochemistryauthors
Lambert M,Bui NDdoi
10.1023/a:1007016403736keywords:
subject
Has Abstractpub_date
1999-12-01 00:00:00pages
101-8issue
1-2eissn
0300-8177issn
1573-4919journal_volume
202pub_type
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