Molecular Mechanism of Pancreatic Bicarbonate Secretion

Min Goo Lee, J. Kim, K. Kim, S. Muallem
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引用次数: 5

Abstract

Thanks to recent progress in availability of molecular and functional techniques it became possible to search for the basic molecular and cellular processes that mediate and control and fluid secretion by the pancreatic duct. The coordinated action of various transporters on the luminal and basolateral membranes of polarized epithelial cells mediates the transepithelial transport, which involves absorption in the resting state and secretion in the stimulated state. The overall process of HCO3 secretion can be divided into two steps. First, in the blood enters the ductal epithelial cells across the basolateral membrane either by simple diffusion in the forms of and or by the action of an transporter, a cotranporter (NBC) identified as pNBC1. Subsequently, the cells secrete to the luminal space using at least two exit mechanisms at the luminal membrane. One of the critical transporters needed for all forms of secretion across the luminal membrane is the cystic fibrosis transmembrane conductance regulator (CFTR). In the resting state the pancreatic duct, and probably other secretory epithelia, absorb Interestingly, CFTR also control this mechanism. In this review, we discuss recent progress in understanding epithelial transport, in particular the nature of the luminal transporters and their regulation by CFTR.
胰腺碳酸氢盐分泌的分子机制
由于分子和功能技术的最新进展,使得寻找介导和控制胰管液体分泌的基本分子和细胞过程成为可能。各种转运蛋白在极化上皮细胞的管腔膜和基底膜上协同作用,介导了经上皮转运,包括静息状态下的吸收和刺激状态下的分泌。HCO3分泌的整体过程可分为两个步骤。首先,血液通过基底外膜进入导管上皮细胞,通过简单的扩散或通过转运蛋白的作用,一种共转运蛋白(NBC)被鉴定为pNBC1。随后,细胞通过至少两种腔膜出口机制分泌到腔空间。囊性纤维化跨膜传导调节因子(CFTR)是所有形式的跨腔膜分泌所需的关键转运蛋白之一。在静息状态下,胰管,也可能是其他分泌上皮,吸收。有趣的是,CFTR也控制着这一机制。在这篇综述中,我们讨论了最近在理解上皮运输方面的进展,特别是管腔转运体的性质及其通过CFTR的调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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