We evaluated the effects of a transient cold shock followed by recovery and incubation at 37 °C on the regulation of heat shock gene expression in the IMR-90 human diploid fibroblasts and HeLa cells in tissue culture. We showed that preincubation of cells at 4 °C induced the synthesis and accumulation of the heat shock proteins (HSPs) upon recovery at 37 °C, and the degree of this induction was directly related to the time that the cells spent at 4 °C. Assays on the abundance of the hsp 70 transcript, the hsp 70 gene promoter activity, and the trimerization and activation of heat shock factor (HSF) to bind to its consensus heat shock element (HSE) provided evidence that this induction of the heat shock response in cells recovering from a transient cold shock is attributable to a transcriptional event mediated by the activation of HSF. Further, the induction was a response to the temperature upshift from 4 to 37 °C as opposed to the 4 °C treatment itself; quantitation of the HSE-binding activity of cells incubated at 4 °C without recovery and incubation at 37 °C gave no evidence of an activated response. Analysis of the effects of protein synthesis inhibitors demonstrated that neither cycloheximide nor puromycin was effective in blocking the induction of HSE-binding activity in cells recovering from a transient cold shock. Experiments on the time course and temperature dependence of this induction of HSE-binding activity showed that the onset, magnitude, and duration of this induction were directly proportional to the severity of the cold stress (measured by time and temperature). We discuss the possible mechanism(s) involved in this induction of the heat shock genes at 37 °C by a transient cold shock and the biological implications of this observation.
|Original language||English (US)|
|Number of pages||8|
|Journal||Journal of Biological Chemistry|
|State||Published - May 20 1994|
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Cell Biology