Protein kinase D: coupling extracellular stimuli to the regulation of cell physiology

被引:112
作者
Fu, Ya [1 ]
Rubin, Charles S. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10461 USA
基金
美国国家卫生研究院;
关键词
protein kinase D; diacylglycerol; PKD effectors; PKD functions; PKD regulation; PKD inhibitors; MATRIX-METALLOPROTEINASE EXPRESSION; D-MEDIATED PHOSPHORYLATION; PLASMA-MEMBRANE TRANSPORT; ACTIVATION LOOP SER(744); HISTONE DEACETYLASE 7; NF-KAPPA-B; IN-VIVO; PROSTATE-CANCER; C-MU; G(Q)-COUPLED RECEPTORS;
D O I
10.1038/embor.2011.139
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
Protein kinase D (PKD) mediates the actions of stimuli that promote diacylglycerol (DAG) biogenesis. By phosphorylating effectors that regulate transcription, fission and polarized transport of Golgi vesicles, as well as cell migration and survival after oxidative stress, PKDs substantially expand the range of physiological processes controlled by DAG. Dysregulated PKDs have been linked to pathologies including heart hypertrophy and cancer invasiveness. Our understanding of PKD regulation by trans-and auto-phosphorylation, as well as the sub-cellular dynamics of PKD substrate phosphorylation, have increased markedly. Selective PKD inhibitors provide new, powerful tools for elucidating the physiological roles of PKDs and potentially treating cardiac disease and cancer.
引用
收藏
页码:785 / 796
页数:12
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