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Endoplasmic reticulum stress downregulates PGC-1α in skeletal muscle through ATF4 and an mTOR-mediated reduction of CRTC2.内质网应激通过激活转录因子4(ATF4)以及哺乳动物雷帕霉素靶蛋白(mTOR)介导的含CREB调节蛋白2(CRTC2)减少,下调骨骼肌中的过氧化物酶体增殖物激活受体γ辅助激活因子1α(PGC-1α)。
Cell Commun Signal. 2022 Apr 15;20(1):53. doi: 10.1186/s12964-022-00865-9.
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New Insights Into the Pivotal Role of CREB-Regulated Transcription Coactivator 1 in Depression and Comorbid Obesity.关于CREB调节转录共激活因子1在抑郁症和共病肥胖症中的关键作用的新见解
Front Mol Neurosci. 2022 Feb 15;15:810641. doi: 10.3389/fnmol.2022.810641. eCollection 2022.
3
A propolis-derived small molecule ameliorates metabolic syndrome in obese mice by targeting the CREB/CRTC2 transcriptional complex.一种源于蜂胶的小分子通过靶向 CREB/CRTC2 转录复合物改善肥胖小鼠的代谢综合征。
Nat Commun. 2022 Jan 11;13(1):246. doi: 10.1038/s41467-021-27533-9.
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Activation of Crtc2/Creb1 in skeletal muscle enhances weight loss during intermittent fasting.在骨骼肌中激活 Crtc2/Creb1 可增强间歇性禁食期间的体重减轻。
FASEB J. 2021 Dec;35(12):e21999. doi: 10.1096/fj.202100171R.
5
Activation of the adipocyte CREB/CRTC pathway in obesity.肥胖症中脂肪细胞 CREB/CRTC 通路的激活。
Commun Biol. 2021 Oct 22;4(1):1214. doi: 10.1038/s42003-021-02735-5.
6
Sam68 promotes hepatic gluconeogenesis via CRTC2.Sam68通过CRTC2促进肝脏糖异生。
Nat Commun. 2021 Jun 7;12(1):3340. doi: 10.1038/s41467-021-23624-9.
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Fate and State of Vascular Smooth Muscle Cells in Atherosclerosis.动脉粥样硬化中血管平滑肌细胞的命运和状态。
Circulation. 2021 May 25;143(21):2110-2116. doi: 10.1161/CIRCULATIONAHA.120.049922. Epub 2021 May 24.
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A kinome screen reveals that Nemo-like kinase is a key suppressor of hepatic gluconeogenesis.激酶组筛选显示,类Nemo激酶是肝脏糖异生的关键抑制因子。
Cell Metab. 2021 Jun 1;33(6):1171-1186.e9. doi: 10.1016/j.cmet.2021.04.006. Epub 2021 May 4.
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Alterations of Gut Microbiota by Overnutrition Impact Gluconeogenic Gene Expression and Insulin Signaling.过度营养引起的肠道微生物组改变影响糖异生基因表达和胰岛素信号。
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CRTC2的生物学功能及其在代谢相关疾病中的作用。

Biological functions of CRTC2 and its role in metabolism-related diseases.

作者信息

Zheng Hong-Yu, Wang Yan-Xia, Zhou Kun, Xie Hai-Lin, Ren Zhong, Liu Hui-Ting, Ou Yang-Shao, Zhou Zhi-Xiang, Jiang Zhi-Sheng

机构信息

Institute of Cardiovascular Disease, Key Lab for Arteriosclerology of Hunan Province, International Joint Laboratory for Arteriosclerotic Disease Research of Hunan Province, University of South China, Hengyang, 421001, China.

出版信息

J Cell Commun Signal. 2023 Sep;17(3):495-506. doi: 10.1007/s12079-023-00730-5. Epub 2023 Mar 1.

DOI:10.1007/s12079-023-00730-5
PMID:36856929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10409973/
Abstract

CREB-regulated transcription coactivator2 (CRTC2 or TORC2) is a transcriptional coactivator of CREB(cAMP response element binding protein), which affects human energy metabolism through cyclic adenosine phosphate pathway, Mammalian target of rapamycin (mTOR) pathway, Sterol regulatory element binding protein 1(SREBP1), Sterol regulatory element binding protein 2 (SREBP2) and other substances Current studies on CRTC2 mainly focus on glucose and lipid metabolism, relevant studies show that CRTC2 can participate in the occurrence and development of related diseases by affecting metabolic homeostasis. It has been found that Crtc2 acts as a signaling regulator for cAMP and Ca2 + signaling pathways in many cell types, and phosphorylation at ser171 and ser275 can regulate downstream biological functions by controlling CRTC2 shuttling between cytoplasm and nucleus.

摘要

CREB调节转录共激活因子2(CRTC2或TORC2)是CREB(环磷酸腺苷反应元件结合蛋白)的转录共激活因子,其通过环磷酸腺苷途径、哺乳动物雷帕霉素靶蛋白(mTOR)途径、固醇调节元件结合蛋白1(SREBP1)、固醇调节元件结合蛋白2(SREBP2)等物质影响人体能量代谢。目前关于CRTC2的研究主要集中在葡萄糖和脂质代谢方面,相关研究表明,CRTC2可通过影响代谢稳态参与相关疾病的发生发展。研究发现,Crtc2在多种细胞类型中作为环磷酸腺苷和Ca2+信号通路的信号调节剂,Ser171和Ser275位点的磷酸化可通过控制CRTC2在细胞质和细胞核之间穿梭来调节下游生物学功能。