Biochemical Journal · 1993 · 50 citations · 19 references
Life SciencesCell BiologyMolecular BiologyCell PhysiologyGene ExpressionProtein TranslationCell SurvivalProtein SynthesisStress Response GenesStress-induced Gene ExpressionStress-responsive Gene RegulationCell Survival AssaysCellular Heat Shock ResponseHeat Shock Protein RegulationHeat Shock ResponseHeat Shock Response GenesHyperosmotic Stress ResponseOsmotic PressureOsmotic Pressure Regulation
Induced expression of the HSP70 gene in 3T3 and SV-3T3 cells was monitored by measurements of the synthesis of HSP70 and of the cellular contents of both HSP70 and its mRNA. The presence of betaine (N-trimethylglycine) at concentrations of 2.5-25 mM decreased the induction of HSP70 gene expression caused by incubation of 3T3 and SV-3T3 cells in hypertonic (0.5 osM) medium. This effect was accompanied by an enhancement of SV-3T3 cell adaptation, assayed by colony formation, to the hyperosmotic conditions. In contrast, the presence of betaine did not affect HSP70 gene expression induced in these cells by heat shock. After 6 h incubation with 25 mM betaine under hypertonic (0.5 osM) conditions the intracellular concentration of betaine in SV-3T3 cells was about 195 mM, compared with about 70 mM under isotonic (0.3 osM) conditions. Hence, with this concentration of extracellular betaine, the marked increase in the accumulation of betaine within the cells presumably counteracts the imposed osmotic pressure and eliminates the signal that otherwise initiates increased expression of the HSP70 gene.
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