NHE3 regulatory complexes

• Published in: Journal of experimental biology Vol. 212; no. Pt 11; pp. 1638 - 1646
• Main Authors: Donowitz, Mark, Mohan, Sachin, Zhu, Cindy Xinjun, Chen, Tian-E, Lin, Rong, Cha, Boyoung, Zachos, Nicholas C, Murtazina, Rakhilya, Sarker, Rafiquel, Li, Xuhang
• Format: Journal Article
• Language: English
• Published: England Company of Biologists 01.06.2009
• Subjects: Animals; Humans; Intestine, Small - metabolism; Mammals; Models, Molecular; Protein Conformation; Review; Sodium Chloride - metabolism; Sodium-Hydrogen Exchanger 3; Sodium-Hydrogen Exchangers - chemistry; Sodium-Hydrogen Exchangers - metabolism
• ISSN: 0022-0949; 1477-9145
• 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.