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胰岛细胞间通讯是正常胰岛素分泌的基础。

Islet-cell-to-cell communication as basis for normal insulin secretion.

作者信息

Bavamian S, Klee P, Britan A, Populaire C, Caille D, Cancela J, Charollais A, Meda P

机构信息

Department of Cell Physiology and Metabolism, University of Geneva, Medical School, Genève, Switzerland.

出版信息

Diabetes Obes Metab. 2007 Nov;9 Suppl 2:118-32. doi: 10.1111/j.1463-1326.2007.00780.x.

Abstract

The emergence of pancreatic islets has necessitated the development of a signalling system for the intra- and inter-islet coordination of beta cells. With evolution, this system has evolved into a complex regulatory network of partially cross-talking pathways, whereby individual cells sense the state of activity of their neighbours and, accordingly, regulate their own level of functioning. A consistent feature of this network in vertebrates is the expression of connexin (Cx)-36-made cell-to-cell channels, which cluster at gap junction domains of the cell membrane, and which adjacent beta cells use to share cytoplasmic ions and small metabolites within individual islets. This chapter reviews what is known about Cx36, and the mechanism whereby this beta-cell connexin significantly regulates insulin secretion. It further outlines other less established functions of the protein and evaluates its potential relevance for the development of novel therapeutic approaches to diabetes.

摘要

胰岛的出现促使一种用于胰岛内和胰岛间β细胞协调的信号系统得以发展。随着进化,这个系统已演变成一个由部分相互作用途径构成的复杂调控网络,通过该网络,单个细胞能够感知其相邻细胞的活动状态,并据此调节自身的功能水平。在脊椎动物中,这个网络的一个一致特征是连接蛋白(Cx)-36构成的细胞间通道的表达,这些通道聚集在细胞膜的缝隙连接区域,相邻的β细胞利用它们在单个胰岛内共享细胞质离子和小代谢物。本章综述了关于Cx36的已知信息,以及这种β细胞连接蛋白显著调节胰岛素分泌的机制。它还概述了该蛋白其他尚未完全明确的功能,并评估了其对于开发新型糖尿病治疗方法的潜在相关性。

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