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从一个角度看寿命的代谢调节。

Metabolic regulation of lifespan from a perspective.

作者信息

Dall Kathrine B, Færgeman Nils J

机构信息

Department of Biochemistry and Molecular Biology, Villum Center for Bioanalytical Sciences, University of Southern Denmark, Campusvej 55, 5230 Odense M, Denmark.

出版信息

Genes Nutr. 2019 Aug 15;14:25. doi: 10.1186/s12263-019-0650-x. eCollection 2019.

Abstract

Decline of cellular functions especially cognitive is a major deficit that arises with age in humans. Harnessing the strengths of small and genetic tractable model systems has revealed key conserved regulatory biochemical and signaling pathways that control aging. Here, we review some of the key signaling and biochemical pathways that coordinate aging processes with special emphasis on as a model system and discuss how nutrients and metabolites can regulate lifespan by coordinating signaling and epigenetic programs. We focus on central nutrient-sensing pathways such as mTOR and insulin/insulin-like growth factor signaling and key transcription factors including the conserved basic helix-loop-helix transcription factor HLH-30/TFEB.

摘要

细胞功能衰退,尤其是认知功能衰退,是人类衰老过程中出现的主要缺陷。利用小型且遗传易处理的模型系统的优势,已揭示出控制衰老的关键保守调节生化和信号通路。在此,我们回顾一些协调衰老过程的关键信号和生化通路,特别强调秀丽隐杆线虫作为一个模型系统,并讨论营养素和代谢物如何通过协调信号和表观遗传程序来调节寿命。我们重点关注中心营养感应通路,如mTOR和胰岛素/胰岛素样生长因子信号通路,以及关键转录因子,包括保守的碱性螺旋-环-螺旋转录因子HLH-30/TFEB。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb00/6694653/1122404b9419/12263_2019_650_Fig1_HTML.jpg

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