Half-lives of plasma membrane Na+/H+ exchangers NHE1-3:: plasma membrane NHE2 has a rapid rate of degradation

被引:45
作者
Cavet, ME
Akhter, S
Murtazina, R
De Medina, FS
Tse, CM
Donowitz, M
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Gastrointestinal Div, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Physiol, Gastrointestinal Div, Baltimore, MD 21205 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2001年 / 281卷 / 06期
关键词
sodium absorption; Caco-2; cells; lysosomes; trafficking;
D O I
10.1152/ajpcell.2001.281.6.C2039
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Na+/H+ exchangers NHE2 and NHE3 are involved in epithelial Na+ and HCO3- absorption. To increase insights into the functions of NHE2 vs. NHE3, we compared their cellular processing with each other and with the housekeeping isoform NHE1. Using biotinylated exchanger, we determined that the half-life of plasma membrane NHE2 was short (3 h) compared with that of NHE1 (24 h) and NHE3 (14 h) in both PS120 fibroblasts and Caco-2 cells. NHE2 transport and plasma membrane levels were reduced by 3 h of Brefeldin A treatment, whereas NHE1 was unaffected. NHE2 was degraded by the lysosomes but not proteosomes, as demonstrated by increasing levels of endocytosed NHE2 protein after inhibition of the lysosomes, but not with proteosome inhibition. Unlike that of NHE3, basal NHE2 transport activity was not affected by phosphatidylinositol 3-kinase inhibition and did not appear to be localized in the juxtanuclear recycling endosome. Therefore, for NHE2, protein degradation and/or protein synthesis probably play important roles in its basal and regulated states. These results suggest fundamental differences in the cellular processing and trafficking of NHE2 and NHE3. These differences may underlie the specialized roles that these exchangers play in epithelial cells.
引用
收藏
页码:C2039 / C2048
页数:10
相关论文
共 41 条
[1]   Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome [J].
Abriel, H ;
Loffing, J ;
Rebhun, JF ;
Pratt, JH ;
Schild, L ;
Horisberger, JD ;
Rotin, D ;
Staub, O .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (05) :667-673
[2]   C-terminal domains of Na+/H+ exchanger isoform 3 are involved in the basal and serum-stimulated membrane trafficking of the exchanger [J].
Akhter, S ;
Cavet, ME ;
Tse, CM ;
Donowitz, M .
BIOCHEMISTRY, 2000, 39 (08) :1990-2000
[3]   Ubiquitin and the control of protein fate in the secretory and endocytic pathways [J].
Bonifacino, JS ;
Weissman, AM .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1998, 14 :19-57
[4]   Na+/H+ exchangers (NHE1-3) have similar turnover numbers but different percentages on the cell surface [J].
Cavet, ME ;
Akhter, S ;
De Medina, FS ;
Donowitz, M ;
Tse, CM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 277 (06) :C1111-C1121
[5]   Immunolocalization of the Na+/H+ exchanger isoform NHE2 in rat kidney [J].
Chambrey, R ;
Warnock, DG ;
Podevin, RA ;
Bruneval, P ;
Mandet, C ;
Bélair, MF ;
Bariéty, J ;
Paillard, M .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1998, 275 (03) :F379-F386
[6]  
CHANTRET I, 1994, J CELL SCI, V107, P213
[7]   Novel amiloride-sensitive sodium-dependent proton secretion in the mouse proximal convoluted tubule [J].
Choi, JY ;
Shah, M ;
Lee, MG ;
Schultheis, PJ ;
Shull, GE ;
Muallem, S ;
Baum, M .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (08) :1141-1146
[8]   Acute regulation of Na+/H+ exchanger NHE3 by parathyroid hormone via NHE3 phosphorylation and dynamin-dependent endocytosis [J].
Collazo, R ;
Fan, LZ ;
Hu, MC ;
Zhao, H ;
Wiederkehr, MR ;
Moe, OW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :31601-31608
[9]   THE NA+/H+ EXCHANGER NHE-1 POSSESSES N-LINKED AND O-LINKED GLYCOSYLATION RESTRICTED TO THE FIRST N-TERMINAL EXTRACELLULAR DOMAIN [J].
COUNILLON, L ;
POUYSSEGUR, J ;
REITHMEIER, RAF .
BIOCHEMISTRY, 1994, 33 (34) :10463-10469
[10]   Biosynthesis and cell surface delivery of the NHE1 isoform of Na+/H+ exchanger in A6 cells [J].
CoupayeGerard, B ;
Bookstein, C ;
Duncan, P ;
Chen, XY ;
Smith, PR ;
Musch, M ;
Ernst, SA ;
Chang, EB ;
Kleyman, TR .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (05) :C1639-C1645