The hepatic circadian clock fine-tunes the lipogenic response to feeding through RORα/γ

被引:53
|
作者
Zhang, Yuxiang [1 ,2 ,3 ]
Papazyan, Romeo [1 ,2 ]
Damle, Manashree [1 ,2 ]
Fang, Bin [1 ,2 ]
Jager, Jennifer [1 ,2 ]
Feng, Dan [1 ,2 ]
Peed, Lindsey C. [1 ,2 ]
Guan, Dongyin [1 ,2 ]
Sun, Zheng [1 ,2 ,4 ,5 ]
Lazar, Mitchell A. [1 ,2 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
[4] Baylor Coll Med, Div Diabet Endocrinol & Metab, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
ROR; liver; circadian; SREBP1c; metabolism; REV-ERB-ALPHA; ORPHAN NUCLEAR RECEPTOR; ELEMENT-BINDING PROTEINS; CLEAVAGE-ACTIVATING PROTEIN; INTEGRATIVE GENOMICS VIEWER; FATTY-ACID SYNTHESIS; LIPID-METABOLISM; GENE-EXPRESSION; DEFICIENT MICE; CROSS-TALK;
D O I
10.1101/gad.302323.117
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Liver lipid metabolism is under intricate temporal control by both the circadian clock and feeding. The interplay between these two mechanisms is not clear. Here we show that liver-specific depletion of nuclear receptors ROR alpha and ROR gamma, key components of the molecular circadian clock, up-regulate expression of lipogenic genes only under fed conditions at Zeitgeber time 22 (ZT22) but not under fasting conditions at ZT22 or ad libitum conditions at ZT10. ROR alpha/gamma controls circadian expression of Insig2, which keeps feeding-induced SREBP1c activation under check. Loss of ROR alpha/gamma causes overactivation of the SREBP-dependent lipogenic response to feeding, exacerbating diet-induced hepatic steatosis. These findings thus establish ROR/INSIG2/SREBP as a molecular pathway by which circadian clock components anticipatorily regulate lipogenic responses to feeding. This highlights the importance of time of day as a consideration in the treatment of liver metabolic disorders.
引用
收藏
页码:1202 / 1211
页数:10
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