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共激活因子结合蛋白PIMT通过MEF2A和GLUT4的转录下调介导肿瘤坏死因子-α诱导的骨骼肌胰岛素抵抗。

Co-activator binding protein PIMT mediates TNF-α induced insulin resistance in skeletal muscle via the transcriptional down-regulation of MEF2A and GLUT4.

作者信息

Kain Vasundhara, Kapadia Bandish, Viswakarma Navin, Seshadri Sriram, Prajapati Bhumika, Jena Prasant K, Teja Meda Chandana Lakshmi, Subramanian Maitreyi, Kaimal Suraj Sashidhara, Kumar Sireesh T, Prakash Babu Phanithi, Thimmapaya Bayar, Reddy Janardan K, Parsa Kishore V L, Misra Parimal

机构信息

Department of Biology, Dr. Reddy's Institute of Life Sciences, University of Hyderabad Campus, Hyderabad, Telangana, India.

Institute of Science, Nirma University, Sarkhej-Gandhinagar Highway, Ahmedabad, Gujarat, India.

出版信息

Sci Rep. 2015 Oct 15;5:15197. doi: 10.1038/srep15197.

Abstract

The mechanisms underlying inflammation induced insulin resistance are poorly understood. Here, we report that the expression of PIMT, a transcriptional co-activator binding protein, was up-regulated in the soleus muscle of high sucrose diet (HSD) induced insulin resistant rats and TNF-α exposed cultured myoblasts. Moreover, TNF-α induced phosphorylation of PIMT at the ERK1/2 target site Ser(298). Wild type (WT) PIMT or phospho-mimic Ser298Asp mutant but not phospho-deficient Ser298Ala PIMT mutant abrogated insulin stimulated glucose uptake by L6 myotubes and neonatal rat skeletal myoblasts. Whereas, PIMT knock down relieved TNF-α inhibited insulin signaling. Mechanistic analysis revealed that PIMT differentially regulated the expression of GLUT4, MEF2A, PGC-1α and HDAC5 in cultured cells and skeletal muscle of Wistar rats. Further characterization showed that PIMT was recruited to GLUT4, MEF2A and HDAC5 promoters and overexpression of PIMT abolished the activity of WT but not MEF2A binding defective mutant GLUT4 promoter. Collectively, we conclude that PIMT mediates TNF-α induced insulin resistance at the skeletal muscle via the transcriptional modulation of GLUT4, MEF2A, PGC-1α and HDAC5 genes.

摘要

炎症诱导胰岛素抵抗的潜在机制目前尚不清楚。在此,我们报告,转录共激活因子结合蛋白PIMT在高蔗糖饮食(HSD)诱导的胰岛素抵抗大鼠的比目鱼肌以及肿瘤坏死因子-α(TNF-α)处理的培养成肌细胞中表达上调。此外,TNF-α可诱导PIMT在细胞外信号调节激酶1/2(ERK1/2)的靶点丝氨酸(Ser)298位点发生磷酸化。野生型(WT)PIMT或磷酸化模拟物Ser298Asp突变体而非磷酸化缺陷型Ser298Ala PIMT突变体可消除L6肌管和新生大鼠骨骼肌成肌细胞中胰岛素刺激的葡萄糖摄取。而敲低PIMT可缓解TNF-α对胰岛素信号的抑制作用。机制分析表明,PIMT在培养细胞和Wistar大鼠骨骼肌中差异调节葡萄糖转运蛋白4(GLUT4)、肌细胞增强因子2A(MEF2A)、过氧化物酶体增殖物激活受体γ共激活因子1α(PGC-1α)和组蛋白去乙酰化酶5(HDAC5)的表达。进一步的特性分析表明,PIMT被招募至GLUT4、MEF2A和HDAC5启动子,且PIMT的过表达消除了WT而非MEF2A结合缺陷型突变体GLUT4启动子的活性。我们总体得出结论,PIMT通过对GLUT4、MEF2A、PGC-1α和HDAC5基因的转录调控介导TNF-α诱导的骨骼肌胰岛素抵抗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/010d/4606566/f9e6bf09a985/srep15197-f1.jpg

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