Molecular basis of circadian rhythmicity in renal physiology and pathophysiology

被引:26
作者
Gumz, Michelle L. [1 ,2 ]
机构
[1] Univ Florida, Dept Med, Div Nephrol Hypertens & Renal Transplantat, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
CLOCK PROTEIN PER1; GENE-EXPRESSION; TUBULE CELLS; ALDOSTERONE; HOMEOSTASIS; HYPERTENSION; RECEPTOR; MAMMALS; SYSTEM; KIDNEY;
D O I
10.1113/EP085781
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In this brief review, an overview of the molecular and physiological evidence for the kidney clock and the implications for the regulation of renal physiology and pathophysiology are presented. Accumulating evidence suggests that the molecular circadian clock acts as a master regulator of gene expression in the kidney. Global transcriptomic approaches have revealed the important finding that there are thousands of genes in the kidney subject to regulation by the molecular clock. Candidate gene approaches have also yielded information regarding regulation of renal sodium transport genes by the molecular clock. To date, the evidence linking the molecular kidney clock to rhythmic renal function provides strong support for the concept that circadian control of gene expression underlies rhythms in physiological function.
引用
收藏
页码:1025 / 1029
页数:5
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