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敲低 Stard3 可减少 3T3-L1 细胞中的线粒体 ROS,从而抑制脂肪生成。

Knocking down Stard3 decreases adipogenesis with decreased mitochondrial ROS in 3T3-L1 cells.

机构信息

Centre for Lipid Research & Key Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Department of Infectious Diseases, The Second Affiliated Hospital, Chongqing Medical University, 400016, Chongqing, China.

Department of Biology, Southern University of Science and Technology, Shenzhen, China.

出版信息

Biochem Biophys Res Commun. 2018 Oct 2;504(2):387-392. doi: 10.1016/j.bbrc.2018.06.030. Epub 2018 Jun 15.

Abstract

Start domain-containing protein 3 (Stard3) plays roles in intracellular cholesterol distribution, however, the role of Stard3 in the adipogenesis of 3T3-L1 preadipocytes remains unclear. We demonstrated that Stard3 expression was significantly increased during the adipogenesis of 3T3-L1 preadipocytes, accompanied by an increase of mitochondrial Reactive oxygen species (ROS). Stard3 knocking-down inhibited 3T3-L1 preadipocyte adipogenesis with decreased mitochondrial ROS levels, while ROS inducer rescued the stard3 silencing 3T3 cells with increased ROS. Moreover, Stard3 silencing reduced the expression of peroxisome proliferator-activated receptor-γ (PPARγ) and CCAAT/enhancer binding protein (C/EBP)α in 3T3- L1 cells. In conclusion, Stard3 enhanced the adipogenesis of preadipocytes by enhancement of cholesterol redistribution to the mitochondrial, increasing mitochondrial ROS production. These results suggest that Stard3 is an essential factor for the 3T3-L1 cells' differentiation.

摘要

启动域包含蛋白 3(Stard3)在细胞内胆固醇分布中发挥作用,然而,Stard3 在 3T3-L1 前脂肪细胞的脂肪生成中的作用尚不清楚。我们证明,Stard3 的表达在前脂肪细胞的脂肪生成过程中显著增加,伴随着线粒体活性氧物质(ROS)的增加。Stard3 敲低抑制 3T3-L1 前脂肪细胞脂肪生成,线粒体 ROS 水平降低,而 ROS 诱导剂挽救了 stard3 沉默的 3T3 细胞,ROS 增加。此外,Stard3 沉默降低了 3T3-L1 细胞中过氧化物酶体增殖物激活受体-γ(PPARγ)和 CCAAT/增强子结合蛋白(C/EBP)α 的表达。总之,Stard3 通过增强胆固醇向线粒体的再分布,增加线粒体 ROS 的产生,增强前脂肪细胞的脂肪生成。这些结果表明,Stard3 是 3T3-L1 细胞分化的必需因素。

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