Emerging Roles of Glucocorticoid Receptor Phosphorylation in Modulating Glucocorticoid Hormone Action in Health and Disease

被引:146
作者
Galliher-Beckley, Amy J. [1 ]
Cidlowski, John A. [1 ]
机构
[1] NIEHS, Mol Endocrinol Grp, Lab Signal Transduct, Dept Hlth & Human Serv,NIH, Res Triangle Pk, NC 27709 USA
关键词
CDK; glucocorticoid receptor; ERK; GSK-3; beta; JNK; p38; MAPK; phosphorylation; N-TERMINAL KINASE; GENE-EXPRESSION; PROTEIN-KINASE; TRANSCRIPTIONAL ACTIVATION; CELLS; SITES; CROSSTALK; APOPTOSIS; ISOFORMS;
D O I
10.1002/iub.245
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glucocorticoids (GCs) are hormones naturally released when the body perceives stress and function to return homeostatic balance within various tissues. Synthetic GCs are widely prescribed therapeutics for the treatment of numerous inflammatory disorders and cancers. The effects of GCs are mediated by their binding and activation of the GC receptor (GR), a transcription factor that is subject to hormone-dependent and -independent phosphorylation on several serine and threonine residues. The GR is phosphorylated by kinases such as MAPKs, CDKs, and GSK-3 beta, and these modifications modulate the transcriptional activity of the GR within cells. Here, we discuss the phosphorylation status of the GR as a mechanism to dictate how cells will ultimately respond to GCs. In doing so, we will review current knowledge about each phosphorylated residue within the GR and their contributions to modulating GC signaling in normal homeostatic physiology and during the progression of disease. (C) 2009 IUBMB IUBMB Life, 61(10): 979-986, 2009
引用
收藏
页码:979 / 986
页数:8
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