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微小RNA在调控β细胞活性方面的新出现的任务。

New emerging tasks for microRNAs in the control of β-cell activities.

作者信息

Guay Claudiane, Regazzi Romano

机构信息

Department of Fundamental Neurosciences, University of Lausanne, Switzerland.

Department of Fundamental Neurosciences, University of Lausanne, Switzerland.

出版信息

Biochim Biophys Acta. 2016 Dec;1861(12 Pt B):2121-2129. doi: 10.1016/j.bbalip.2016.05.003. Epub 2016 May 10.

DOI:10.1016/j.bbalip.2016.05.003
PMID:27178175
Abstract

MicroRNAs are key regulators of β-cell physiology. They participate to the differentiation of insulin-producing cells and are instrumental for the acquisition of their unique secretory properties. Moreover, they contribute to the adaptation of β-cells to conditions of increased insulin demand and, if expressed at inappropriate levels, certain microRNAs cause β-cell dysfunction and promote the development of different forms of diabetes mellitus. While these functions are increasingly better understood, additional tasks for these small non-coding RNAs have been recently unveiled. Thus, microRNAs are emerging as signaling molecules of a novel exosome-mediated cell-to-cell communication mode permitting a coordinated response of the β-cells to inflammatory conditions and to modifications in the insulin demand. These discoveries raise a number of important issues that once addressed promise to shed new light on the molecular mechanism governing the functions of the β-cells under normal and disease states. This article is part of a Special Issue entitled: MicroRNAs and lipid/energy metabolism and related diseases edited by Carlos Fernández-Hernando and Yajaira Suárez.

摘要

微小RNA是β细胞生理学的关键调节因子。它们参与胰岛素生成细胞的分化,并对其独特分泌特性的获得起重要作用。此外,它们有助于β细胞适应胰岛素需求增加的情况,并且如果某些微小RNA以不适当的水平表达,会导致β细胞功能障碍并促进不同形式糖尿病的发展。虽然对这些功能的理解越来越深入,但这些小的非编码RNA的其他作用最近也被揭示出来。因此,微小RNA正成为一种新型外泌体介导的细胞间通讯模式的信号分子,使β细胞能够对炎症状态和胰岛素需求的变化做出协调反应。这些发现提出了许多重要问题,一旦得到解决,有望为正常和疾病状态下β细胞功能的分子机制提供新的线索。本文是由卡洛斯·费尔南德斯 - 埃尔南多和亚贾伊拉·苏亚雷斯编辑的名为《微小RNA与脂质/能量代谢及相关疾病》特刊的一部分。

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