Gurney Michael A, Laubitz Daniel, Ghishan Fayez K, Kiela Pawel R
Department of Pediatrics - Steele Children's Research Center, University of Arizona, Tucson, AZ.
Department of Pediatrics - Steele Children's Research Center, University of Arizona, Tucson, AZ; Department of Immunobiology, University of Arizona, Tucson, AZ.
Cell Mol Gastroenterol Hepatol. 2017 Jan;3(1):27-40. doi: 10.1016/j.jcmgh.2016.09.010.
Several members of the family of Na/H exchangers are expressed in the gut, with varying expression patterns and cellular localization. Not only do they participate in the regulation of basic epithelial cell functions, including control of transepithelial Na absorption, intracellular pH (pH ), cell volume, and nutrient absorption, but also in cellular proliferation, migration, and apoptosis. Additionally, they modulate the extracellular milieu in order to facilitate other nutrient absorption and to regulate the intestinal microbial microenvironment. Na/H exchangers are frequent targets of inhibition in gastrointestinal pathologies, either by intrinsic factors (e.g. bile acids, inflammatory mediators) or infectious agents and associated microbial toxins. Based on emerging evidence, disruption of NHE activity via impaired expression or function of respective isoforms may contribute not only to local and systemic electrolyte imbalance, but also to the disease severity via multiple mechanisms. Here, we review the current state of knowledge about the roles Na/H exchangers play in the pathogenesis of disorders of diverse origin and affecting a range of GI tissues.
钠氢交换体家族的几个成员在肠道中表达,具有不同的表达模式和细胞定位。它们不仅参与基本上皮细胞功能的调节,包括跨上皮钠吸收、细胞内pH值(pH i)、细胞体积和营养物质吸收的控制,还参与细胞增殖、迁移和凋亡。此外,它们调节细胞外环境,以促进其他营养物质的吸收并调节肠道微生物微环境。在胃肠道疾病中,钠氢交换体经常受到抑制,无论是受到内在因素(如胆汁酸、炎症介质)还是感染因子及相关微生物毒素的影响。基于新出现的证据,通过各自异构体表达或功能受损而破坏NHE活性,不仅可能导致局部和全身电解质失衡,还可能通过多种机制导致疾病严重程度增加。在此,我们综述了目前关于钠氢交换体在多种起源且影响一系列胃肠道组织的疾病发病机制中所起作用的知识现状。