Biological Sciences, Tokyo Institute of Technology, Yokohama, Japan.
Annu Rev Physiol. 2011;73:261-81. doi: 10.1146/annurev-physiol-012110-142244.
Na(+) and Cl(-) movement across the intestinal epithelium occurs by several interconnected mechanisms: (a) nutrient-coupled Na(+) absorption, (b) electroneutral NaCl absorption, (c) electrogenic Cl(-) secretion by CFTR, and (d) electrogenic Na(+) absorption by ENaC. All these transport modes require a favorable electrochemical gradient maintained by the basolateral Na(+)/K(+)-ATPase, a Cl(-) channel, and K(+) channels. Electroneutral NaCl absorption is observed from the small intestine to the distal colon. This transport is mediated by apical Na(+)/H(+) (NHE2/3) and Cl(-)/HCO(3)(-) (Slc26a3/a6 and others) exchangers that provide the major route of NaCl absorption. Electroneutral NaCl absorption and Cl(-) secretion by CFTR are oppositely regulated by the autonomic nerve system, the immune system, and the endocrine system via PKAα, PKCα, cGKII, and/or SGK1. This integrated regulation requires the formation of macromolecular complexes, which are mediated by the NHERF family of scaffold proteins and involve internalization of NHE3. Through use of knockout mice and human mutations, a more detailed understanding of the integrated as well as subtle regulation of electroneutral NaCl absorption by the mammalian intestine has emerged.
肠上皮细胞中的 Na(+)和 Cl(-)转运是通过多种相互关联的机制实现的:(a) 营养物偶联的 Na(+)吸收,(b) 电中性 NaCl 吸收,(c) CFTR 介导的电致 Cl(-)分泌,以及 (d) ENaC 介导的电致 Na(+)吸收。所有这些转运模式都需要由基底外侧 Na(+)/K(+)-ATP 酶、Cl(-)通道和 K(+)通道维持有利的电化学梯度。电中性的 NaCl 吸收从小肠到远端结肠都有观察到。这种转运是由顶端 Na(+)/H(+)(NHE2/3)和 Cl(-)/HCO(3)(-)(Slc26a3/a6 等)交换体介导的,它们提供了 NaCl 吸收的主要途径。电中性的 NaCl 吸收和 CFTR 介导的 Cl(-)分泌通过自主神经系统、免疫系统和内分泌系统通过 PKAα、PKCα、cGKII 和/或 SGK1 进行反向调节。这种综合调节需要形成大分子复合物,这是由 NHERF 家族支架蛋白介导的,并涉及 NHE3 的内化。通过使用敲除小鼠和人类突变,人们对哺乳动物肠道中电中性 NaCl 吸收的综合和微妙调节有了更详细的了解。