1. Heat shock mimics glucocorticoid effects on IFN-gamma-induced Fc gamma RI and Ia messenger RNA expression in mouse peritoneal macrophages.
- Author
-
Sivo J, Harmon JM, and Vogel SN
- Subjects
- Animals, Cells, Cultured, Culture Media, Serum-Free pharmacology, Dexamethasone antagonists & inhibitors, Female, Gene Expression Regulation drug effects, Histocompatibility Antigens Class II drug effects, Macrophages, Peritoneal drug effects, Mice, Mice, Inbred C3H, Mifepristone pharmacology, RNA, Messenger biosynthesis, Receptors, Glucocorticoid drug effects, Receptors, IgG genetics, Dexamethasone toxicity, Histocompatibility Antigens Class II genetics, Hot Temperature adverse effects, Interferon-gamma drug effects, Interferon-gamma pharmacology, Macrophages, Peritoneal metabolism, RNA, Messenger drug effects, Receptors, IgG biosynthesis, Receptors, IgG drug effects
- Abstract
Glucocorticoids activate or repress the expression of different genes. In murine macrophages, glucocorticoids exert opposing effects on the IFN-gamma-induced expression of Fc gamma RI and Ia mRNA and cell surface expression; they enhance IFN-gamma-induced Fc gamma RI mRNA and protein expression, yet inhibit IFN-gamma-induced Ia mRNA and protein expression. Recently, in transfected cell lines, heat shock (HS) has been shown to promote nuclear accumulation of the glucocorticoid receptor (GR), resulting in potentiation of certain GR-mediated responses. In this study, we compared the effects of HS and dexamethasone (DEX) treatment on the IFN-gamma induction of Fc gamma RI and Ia mRNA in murine primary peritoneal macrophages. Our results show that HS exerted the same opposing effects on these IFN-gamma-responsive genes as DEX at 37 degrees C. The glucocorticoid antagonist RU 486 blocked both DEX and HS-induced enhancement of IFN-gamma induction of Fc gamma RI, suggesting a common GR-mediated mechanism. While RU 486 also reversed DEX-induced repression of Ia mRNA expression, supporting a GR-mediated action, it did not affect HS-mediated repression, raising the possibility of a ligand-independent HS response pathway.
- Published
- 1996