APICAL NA+/H+ EXCHANGERS IN THE MAMMALIAN GASTROINTESTINAL TRACT

被引:0
作者
Kiela, P. R. [1 ]
Xu, H.
Ghishan, F. K.
机构
[1] Univ Arizona, Hlth Sci Ctr, Dept Pediat, Steele Childrens Res Ctr, Tucson, AZ 85724 USA
来源
JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY | 2006年 / 57卷
基金
美国国家卫生研究院;
关键词
Na(+)/H(+) exchangers; absorption; brush border; postnatal development;
D O I
暂无
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The Slc9a family of nine Na(+)/H(+) exchangers (NHE) plays a critical role in neutral sodium absorption in the mammalian intestine as well as other absorptive and secretory epithelia of digestive organs. These transport proteins mediate the electroneutral exchange of Na(+) and H(+) and are crucial in a variety of physiological processes, including the fine tuning of intracellular pH, cell volume control and systemic electrolyte, acid-base and fluid volume homeostasis. Here, we review the role of the Na(+)/H(+) exchange mechanism as it relates to the physiology of organs and cells involved in nutrient absorption, and we describe physiological and molecular aspects of individual isoforms, including their structure, tissue-, and subcellular distribution, as well as their regulation by physiological stimuli at the transcriptional and post-transcriptional levels. A particular emphasis is placed on Na(+)/H(+) exchanger isoforms expressed on the apical (brush border) membrane of the epithelial cells, and the consequences of gene-targeted mutation of individual isoforms are discussed in the context of the physiology of digestive organs. Where available, we also provide a review of pathophysiological states related to aberrant expression and/or activity of Na(+)/H(+) exchangers within the confines of the digestive system.
引用
收藏
页码:51 / 79
页数:29
相关论文
共 180 条
[1]   The Na+/H+ exchanger isoform 2 is the predominant NHE isoform in murine colonic crypts and its lack causes NHE3 upregulation [J].
Bachmann, O ;
Riederer, B ;
Rossmann, H ;
Groos, S ;
Schultheis, PJ ;
Shull, GE ;
Gregor, M ;
Manns, MP ;
Seidler, U .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2004, 287 (01) :G125-G133
[2]   Transcriptional regulation of rat Na+/H+ exchanger isoform-2 (NHE-2) gene by Sp1 transcription factor [J].
Bai, LQ ;
Collins, JF ;
Xu, H ;
Ghishan, FK .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (05) :C1168-C1175
[3]   Characterization of cis-elements required for osmotic response of rat Na+/H+ exchanger-2 (NHE-2) gene [J].
Bai, LQ ;
Collins, JF ;
Muller, YL ;
Xu, H ;
Kiela, PR ;
Ghishan, FK .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 277 (04) :R1112-R1119
[4]   Mechanisms of diarrhea in the interleukin-2-deficient mouse model of colonic inflammation [J].
Barmeyer, C ;
Harren, M ;
Schmitz, H ;
Heinzel-Pleines, U ;
Mankertz, J ;
Seidler, U ;
Horak, I ;
Wiedenmann, B ;
Fromm, M ;
Schulzke, JD .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2004, 286 (02) :G244-G252
[5]   Na+/H+ exchanger NHE1 as plasma membrane scaffold in the assembly of signaling complexes [J].
Baumgartner, M ;
Patel, H ;
Barber, DL .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2004, 287 (04) :C844-C850
[6]   AMILORIDE - A MOLECULAR PROBE OF SODIUM-TRANSPORT IN TISSUES AND CELLS [J].
BENOS, DJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 242 (03) :C131-C145
[7]   Membrane topology of NHE3 - Epitopes within the carboxyl-terminal hydrophilic domain are exoplasmic [J].
Biemesderfer, D ;
DeGray, B ;
Aronson, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (20) :12391-12396
[8]  
Binder HJ, 2000, ANN NY ACAD SCI, V915, P43
[9]   Novel transport properties of colonic crypt cells: Fluid absorption and Cl-dependent Na-H exchange [J].
Binder, HJ ;
Singh, SK ;
Geibel, JP ;
Rajendran, VM .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 1997, 118 (02) :265-269
[10]   Glycosylation of the Na+/H+ exchanger isoform NHE-3 is species specific [J].
Bizal, GL ;
Howard, RL ;
Bookstein, C ;
Rao, MC ;
Chang, EB ;
Soleimani, M .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1996, 128 (03) :304-312