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Response of human immunodeficiency virus long terminal repeat to growth factors and hormones.
15
Citations
20
References
1990
Year
Viral ReplicationHuman GrowthImmunologyHuman RetrovirusResistance Mutation (Virology)Hiv LtrPrimary ImmunodeficiencyGrowth HormoneVirologyChronic Viral InfectionHivEndocrinologyPharmacologyCell BiologyGene ExpressionAids PathogenesisSvtghiv-1 Transfectant CellsLong Terminal RepeatAntiviral ResponseGrowth FactorsMedicine
We have employed a recombinant plasmid, pBHIV1, carrying the long terminal repeat (LTR) of the human immunodeficiency virus-1 (HIV-1) linked to the reporter chloramphenicol acetyl transferase (cat) gene and to the aminoglycoside phosphotransferase (aph) gene as a selectable marker. We have introduced pBHIV1 in rat 208F and human MRCSV40TGR fibroblasts and obtained stable geneticin resistant RFBHIV1-1 and SVTGHIV-1 transfectant cells respectively. Both RFBHIV1-1 and SVTGHIV1-1 cells express CAT activity from the HIV LTR promoter. The response to insulin, epidermal growth factor, hydrocortisone and dexamethasone was studied on the LTR regulated CAT activity in both cell lines. It was found that, at optimal concentrations, insulin, epidermal growth factor and hydrocortisone regulate positively the expression of CAT from the HIV LTR in rat RFBHIV1-1 but not in human SVTGHIV1-1 cells. On the other hand dexamethasone at 10(-5) M stimulated CAT activity in both types of cells.
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