ETB receptor activation causes exocytic insertion of NHE3 in OKP cells

被引:53
|
作者
Peng, Y
Amemiya, M
Yang, XJ
Fan, LZ
Moe, OW
Yin, H
Preisig, PA
Yanagisawa, M
Alpern, RJ
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75235 USA
[2] Jichi Med Sch, Dept Internal Med, Minami Kawachi, Tochigi 3290498, Japan
[3] Dallas Vet Affairs Med Ctr, Dallas, TX 75216 USA
[4] Univ Texas, SW Med Ctr, Dept Physiol, Dallas, TX 75235 USA
[5] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Dallas, TX 75235 USA
关键词
sodium/hydrogen antiporter; sodium/hydrogen exchanger 3; opossum kidney clone 3; endothelin; membrane trafficking; proximal tubule;
D O I
10.1152/ajprenal.2001.280.1.F34
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Endothelin-1 (ET-1) activates sodium/hydrogen exchanger 3 (NHE3) in opossum kidney clone P (OKP) cells expressing ETB receptors. ET-1 (10(-8) M) caused a two- to threefold increase in apical membrane NHE3 (assessed by surface biotinylation), in the absence of a change in total cellular NHE3. A maximal effect was achieved within 15 min. The increase in apical NHE3 was not blocked by cytochalasin D but was blocked by latrunculin B, which also prevented the ET-1-induced increase in NHE3 activity. Endocytic internalization of NHE3, measured as protection of biotinylated NHE3 from the membrane-impermeant, sulfhydryl-reducing agent MesNa was minimal within 35 min and was not regulated by ET-1. Exocytic insertion of NHE3, measured as the appearance of biotinylated NHE3 after the blockade of reactive sites with sulfo-NHS-acetate, was increased in response to ET-1. These studies demonstrate that ET-1 induces net trafficking of NHE3 to the apical membrane that is mediated by enhanced exocytic insertion and is required for increased NHE3 activity.
引用
收藏
页码:F34 / F42
页数:9
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