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RMR 相关 DNAJC6 对 3T3-L1 前脂肪细胞成脂分化和线粒体功能的基因调控作用。

Gene regulation of RMR-related DNAJC6 on adipogenesis and mitochondria function in 3T3-L1 preadipocytes.

机构信息

Department of Food & Nutrition, Sungshin Women's University, Seoul, 01133, Republic of Korea; Research Institute of Obesity Science, Sungshin Women's University, Seoul, 01133, Republic of Korea.

Department of Food & Nutrition, Sungshin Women's University, Seoul, 01133, Republic of Korea; Research Institute of Obesity Science, Sungshin Women's University, Seoul, 01133, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2023 Sep 10;672:1-9. doi: 10.1016/j.bbrc.2023.06.037. Epub 2023 Jun 12.

Abstract

In the pilot GWAS of children obesity, DNAJC6 gene was found as a regulator for resting metabolic rate (RMR) and obesity in children aged 8-9 years. To investigate whether DNAJC6 gene regulated obesity and energy metabolism, the physiological mechanisms during adipogenesis of 3T3-L1 preadipocytes were confirmed after DNAJC6 gene was overexpressed or inhibited. Overexpressing DNAJC6 gene maintained a 3T3-L1 preadipocyte status during cell differentiation (MTT, ORO, DAPI/BODIPY). It suppressed adipogenesis and adipokine production (leptin, adiponectin), insulin signaling with IRS-GLUT4 system (RT-PCR, Western blotting), and mitochondrial function (Mito Stress Test). DNAJC6 overexpressed cells inhibited mTOR expression, but maintained LC3 expression at a high level, indicating that autophagy occurred and energy was obtained. However, when DNAJC6 gene was inhibited, fat synthesis factor was highly expressed during differentiation (PPARr, C/EBPa, aP2, etc) and the intracellular stress level increased accordingly, which affected the reduction of reserve respiratory capacity during mitochondrial respiration. Our study confirmed gene regulation of DNAJC6, overexpression or inhibition, affects adipogenesis with energy metabolism and mitochondrial functions. This basic data can be used for clinic obesity studies to control an energy imbalance.

摘要

在儿童肥胖的初步 GWAS 研究中,发现 DNAJC6 基因是调节 8-9 岁儿童静息代谢率 (RMR) 和肥胖的基因。为了研究 DNAJC6 基因是否调节肥胖和能量代谢,在过表达或抑制 DNAJC6 基因后,确认了 3T3-L1 前脂肪细胞成脂分化过程中的生理机制。过表达 DNAJC6 基因可维持 3T3-L1 前脂肪细胞在细胞分化过程中的状态(MTT、ORO、DAPI/BODIPY)。它抑制脂肪生成和脂肪细胞因子的产生(瘦素、脂联素)、胰岛素信号转导 IRS-GLUT4 系统(RT-PCR、Western blot)和线粒体功能(Mito Stress Test)。过表达 DNAJC6 的细胞抑制了 mTOR 的表达,但维持了 LC3 的高水平表达,表明自噬发生并获得了能量。然而,当抑制 DNAJC6 基因时,分化过程中脂肪合成因子高度表达(PPARr、C/EBPa、aP2 等),细胞内应激水平相应增加,这影响了线粒体呼吸过程中储备呼吸能力的降低。我们的研究证实了 DNAJC6 基因的调控,无论是过表达还是抑制,都会影响脂肪生成和能量代谢以及线粒体功能。这些基础数据可用于临床肥胖研究以控制能量失衡。

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