期刊
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
卷 18, 期 5, 页码 439-448出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MNH.0b013e32832f125e
关键词
coagulation; fibrosis; hypertension; inflammation; metabolic syndrome
资金
- Deutsche Forschungsgemeinschaft
- National Institutes of Health [NIH-R01 DK56248, NIH-P30DK079337]
Purpose of review The role of serum and glucocorticoid-inducible kinase 1 (SGK1) in renal physiology and pathophysiology is reviewed with particular emphasis on recent advances. Recent findings The mammalian target of rapamycin complex 2 has been shown to phosphorylate SGK1 at Ser(422) (the so-called hydrophobic motif). Ser(397) and Ser(401) are two additional SGK1-phosphorylation sites required for maximal SGK1 activity. A 5' variant alternate transcript of human Sgk1 has been identified that is widely expressed and shows improved stability, enhanced membrane association, and greater stimulation of epithelial Na+ transport. SGK1 is essential for optimal processing of the epithelial sodium channel and also regulates the expression of the Na+-Cl- cotransporter. With regard to pathophysiology, SGK1 participates in the stimulation of renal tubular glucose transport in diabetes, the renal profibrotic effect of both angiotensin II and aldosterone, and in fetal programing of arterial hypertension. Summary The outlined recent findings advanced our understanding of the molecular regulation of SGK1 as well as the role of the kinase in renal physiology and the pathophysiology of renal disease and hypertension. Future studies using pharmacological inhibitors of SGK1 will reveal the utility of the kinase as a new therapeutic target.
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