期刊
MOLECULAR AND CELLULAR BIOLOGY
卷 28, 期 24, 页码 7309-7322出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.00808-08
关键词
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资金
- NIH National Institute of Environmental Health Sciences [Z01E5090057-12]
Aberrant glycogen synthase kinase 3 beta (GSK-3 beta) activity is associated with the progression of several pathological conditions such as diabetes, Alzheimer's, and cancer. GSK-3 beta regulates cellular processes by directly phosphorylating metabolic enzymes and transcription factors. Here, we discovered a new target for GSK-3 beta phosphorylation: the human glucocorticoid receptor (GR). Glucocorticoid signaling is essential for life and regulates diverse biological functions from cell growth to metabolism to apoptosis. Specifically, we found hormone-dependent GR phosphorylation on serine 404 by GSK-3 beta. Cells expressing a GR that is incapable of GSK-3 beta phosphorylation had a redirection of the global transcriptional response to hormone, including the activation of additional signaling pathways, in part due to the altered ability of unphosphorylatable GR to recruit transcriptional cofactors CBP/p300 and the p65 (RelA) subunit of NF-kappa B. Furthermore, GSK-3 beta-mediated GR phosphorylation inhibited glucocorticoid-dependent NF-kappa B transrepression and attenuated the glucocorticoid-dependent cell death of osteoblasts. Collectively, our results describe a novel convergence point of the GSK-3 beta and the GR pathways, resulting in altered hormone-regulated signaling. Our results also provide a mechanism by which GSK-3 beta activity can dictate how cells will ultimately respond to glucocorticoids.
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