Department of Clinical and Molecular Hepatology, Institute of Medical Research A Lanari-IDIM, University of Buenos Aires-National Council of Scientific and Technological Research (CONICET), Ciudad Autónoma de Buenos Aires, Argentina.
Curr Diab Rep. 2013 Apr;13(2):229-37. doi: 10.1007/s11892-012-0361-9.
In this article, we review the current knowledge of and recent insights into the role of epigenetic factors in the development of insulin resistance (IR), with emphasis on peroxisome proliferator-activated receptor gamma coactivator 1α (PPARGC1A or PGC1α) methylation on fetal programming and liver modulation of glucose-related phenotypes. We discuss the pathogenesis of IR beyond the integrity of β-cell function and illustrate the novel concept of mitochondrial epigenetics to explain the pathobiology of metabolic-syndrome-related phenotypes. Moreover, we discuss whether epigenetic marks in genes of the circadian rhythm system are able to modulate insulin/glucose-related metabolic functions and place hypoxia inducible factor 1 α (HIF1α) as a part of the master CLOCK gene/protein interaction network that might modulate IR. Finally, we highlight relevant information about epigenetic marks and IR so that clinicians practicing in the community may envision future areas of medical intervention and predict putative biomarkers for early disease detection.
在本文中,我们回顾了表观遗传因素在胰岛素抵抗(IR)发展中的作用的现有知识和最新见解,重点介绍了过氧化物酶体增殖物激活受体γ共激活因子 1α(PPARGC1A 或 PGC1α)在胎儿编程中的甲基化以及肝脏对葡萄糖相关表型的调节。我们讨论了超越β细胞功能完整性的 IR 发病机制,并阐述了线粒体表观遗传学的新概念,以解释代谢综合征相关表型的病理生物学。此外,我们还讨论了生物钟系统基因中的表观遗传标记是否能够调节胰岛素/葡萄糖相关的代谢功能,并将缺氧诱导因子 1α(HIF1α)作为可能调节 IR 的主时钟基因/蛋白相互作用网络的一部分。最后,我们强调了与表观遗传标记和 IR 相关的信息,以便在社区中执业的临床医生可以设想未来的医学干预领域,并预测早期疾病检测的潜在生物标志物。