Magro Maria Grazia, Solimena Michele
Molecular Diabetology, Paul Langerhans Institute Dresden, TU Dresden ; German Center for Diabetes Research (DZD e.V.), Fetscherstrasse 74, 01307 Dresden, Germany.
Mol Metab. 2013 Sep 25;2(4):348-55. doi: 10.1016/j.molmet.2013.09.003.
β-cells of the pancreatic islets are highly specialized and high-throughput units for the production of insulin, the key hormone for maintenance of glucose homeostasis. Elevation of extracellular glucose and/or GLP-1 levels triggers a rapid upregulation of insulin biosynthesis through the activation of post-transcriptional mechanisms. RNA-binding proteins are emerging as key factors in the regulation of these mechanisms as well as in other aspects of β-cell function and glucose homeostasis at large, and thus may be implicated in the pathogenesis of diabetes. Here we review current research in the field, with a major emphasis on RNA-binding proteins that control biosynthesis of insulin and other components of the insulin secretory granules by modulating the stability and translation of their mRNAs.
胰岛的β细胞是高度特化且用于产生胰岛素的高通量单元,胰岛素是维持葡萄糖稳态的关键激素。细胞外葡萄糖和/或胰高血糖素样肽-1(GLP-1)水平的升高通过激活转录后机制触发胰岛素生物合成的快速上调。RNA结合蛋白正成为这些机制调节以及β细胞功能和整体葡萄糖稳态其他方面的关键因素,因此可能与糖尿病的发病机制有关。在此,我们综述该领域的当前研究,主要侧重于通过调节胰岛素和胰岛素分泌颗粒其他成分的mRNA稳定性和翻译来控制其生物合成的RNA结合蛋白。