Donowitz Mark, Mohan Sachin, Zhu Cindy Xinjun, Chen Tian-E, Lin Rong, Cha Boyoung, Zachos Nicholas C, Murtazina Rakhilya, Sarker Rafiquel, Li Xuhang
Johns Hopkins University School of Medicine, 720 Rutland Avenue Baltimore, MD 21205, USA.
J Exp Biol. 2009 Jun;212(Pt 11):1638-46. doi: 10.1242/jeb.028605.
The epithelial brush border Na/H exchanger NHE3 is active under basal conditions and functions as part of neutral NaCl absorption in the intestine and renal proximal tubule, where it accounts for the majority of total Na absorbed. NHE3 is highly regulated. Both stimulation and inhibition occur post-prandially. This digestion related regulation of NHE3 is mimicked by multiple extracellular agonists and intracellular second messengers. The regulation of NHE3 depends on its C-terminal cytoplasmic domain, which acts as a scaffold to bind multiple regulatory proteins and links NHE3 to the cytoskeleton. The cytoskeletal association occurs by both direct binding to ezrin and by indirect binding via ezrin binding to the C-terminus of the multi-PDZ domain containing proteins NHERF1 and NHERF2. This is a review of the domain structure of NHE3 and of the scaffolding function and role in the regulation of NHE3 of the NHE3 C-terminal domain.
上皮刷状缘钠/氢交换体NHE3在基础条件下具有活性,是肠道和肾近端小管中性氯化钠吸收的一部分,在这些部位它占总钠吸收量的大部分。NHE3受到高度调节。餐后既会出现刺激也会出现抑制。NHE3的这种与消化相关的调节被多种细胞外激动剂和细胞内第二信使模拟。NHE3的调节取决于其C末端胞质结构域,该结构域作为一个支架,结合多种调节蛋白并将NHE3与细胞骨架相连。细胞骨架的结合通过直接与埃兹蛋白结合以及通过埃兹蛋白间接结合到含有多PDZ结构域的蛋白NHERF1和NHERF2的C末端来实现。本文综述了NHE3的结构域结构以及NHE3 C末端结构域的支架功能及其在NHE3调节中的作用。