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敲低 NYGGF4(PID1)可挽救 FCCP 诱导的 3T3-L1 脂肪细胞胰岛素抵抗和线粒体功能障碍。

Knockdown of NYGGF4 (PID1) rescues insulin resistance and mitochondrial dysfunction induced by FCCP in 3T3-L1 adipocytes.

机构信息

Department of Pediatrics, Nanjing Maternity and Child Health Hospital of Nanjing Medical University, Nanjing 210004, China.

出版信息

Mitochondrion. 2012 Nov;12(6):600-6. doi: 10.1016/j.mito.2012.10.008. Epub 2012 Oct 22.

Abstract

NYGGF4 is a recently identified gene that is involved in obesity-associated insulin resistance. Previous data from this laboratory have demonstrated that NYGGF4 overexpression might contribute to the development of insulin resistance (IR) and to mitochondrial dysfunction. Additionally, NYGGF4 knockdown enhanced insulin sensitivity and mitochondrial function in 3T3-L1 adipocytes. We designed this study to determine whether silencing of NYGGF4 in 3T3-L1 adipocytes could rescue the effect of insulin sensitivity and mitochondrial function induced by the cyanide p-trifluoromethoxyphenyl-hydrazone (FCCP), a mitochondrion uncoupler, to ascertain further the mechanism of NYGGF4 involvement in obesity-associated insulin resistance. We found that 3T3-L1 adipocytes, incubated with 5μM FCCP for 12h, had decreased levels of insulin-stimulated glucose uptake and had impaired insulin-stimulated GLUT4 translocation. Silencing also diminished insulin-stimulated tyrosinephosphorylation of IRS-1 and serine phosphorylation of Akt. This phenomenon contrasts with the effect of NYGGF4 knockdown on insulin sensitivity and describes the regulatory function of NYGGF4 in adipocytes insulin sensitivity. We next analyzed the mitochondrial function in NYGGF4-silenced adipocytes incubated with FCCP. NYGGF4 knockdown partly rescued the dissipation of mitochondrial mass, mitochondrial DNA, intracellular ATP synthesis, and intracellular reactive oxygen species (ROS) production occurred following the addition of FCCP, as well as inhibition of mitochondrial transmembrane potential (ΔΨm) in 3T3-L1 adipocytes incubated with FCCP. Collectively, our results suggested that addition of silencing NYGGF4 partly rescued the effect of insulin resistance and mitochondrial dysfunction in NYGGF4 silenced 3T3-L1 adipocytes incubated with FCCP, which might explain the involvement of NYGGF4-induced IR and the development of NYGGF4 in mitochondrial function.

摘要

NYGGF4 是一个最近被鉴定的基因,它与肥胖相关的胰岛素抵抗有关。本实验室之前的数据表明,NYGGF4 的过表达可能导致胰岛素抵抗(IR)和线粒体功能障碍。此外,NYGGF4 的敲低增强了 3T3-L1 脂肪细胞中的胰岛素敏感性和线粒体功能。我们设计了这项研究,以确定沉默 3T3-L1 脂肪细胞中的 NYGGF4 是否可以挽救氰化物 p-三氟甲氧基苯腙(FCCP)诱导的胰岛素敏感性和线粒体功能的作用,FCCP 是一种线粒体解偶联剂,以进一步确定 NYGGF4 参与肥胖相关胰岛素抵抗的机制。我们发现,用 5μM FCCP 孵育 12 小时的 3T3-L1 脂肪细胞,胰岛素刺激的葡萄糖摄取水平降低,并且胰岛素刺激的 GLUT4 易位受损。沉默还减少了胰岛素刺激的 IRS-1 酪氨酸磷酸化和 Akt 的丝氨酸磷酸化。这种现象与 NYGGF4 敲低对胰岛素敏感性的影响形成对比,并描述了 NYGGF4 在脂肪细胞胰岛素敏感性中的调节功能。我们接下来分析了用 FCCP 孵育的 NYGGF4 沉默的脂肪细胞中的线粒体功能。NYGGF4 的敲低部分挽救了 FCCP 加入后线粒体质量、线粒体 DNA、细胞内 ATP 合成和细胞内活性氧(ROS)产生的耗散,以及 FCCP 孵育的 3T3-L1 脂肪细胞中线粒体跨膜电位(ΔΨm)的抑制。总之,我们的结果表明,沉默 NYGGF4 的加入部分挽救了 FCCP 孵育的 NYGGF4 沉默 3T3-L1 脂肪细胞中胰岛素抵抗和线粒体功能障碍的作用,这可能解释了 NYGGF4 诱导的 IR 和 NYGGF4 在线粒体功能中的作用。

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