Shank2 associates with and regulates Na+/H+ exchanger 3

被引:48
|
作者
Han, W
Kim, KH
Jo, MJ
Lee, JH
Yang, J
Doctor, RB
Moe, OW
Lee, J
Kim, E
Lee, MG [1 ]
机构
[1] Yonsei Univ, Coll Med, Dept Pharmacol,Inst Gastroenterol, Brain Korea 21 Project Med Sci, Seoul 120752, South Korea
[2] Korea Adv Inst Sci & Technol, Creat Res Ctr Synaptogenesis, Taejon 305701, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
[4] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80439 USA
[5] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
[6] Pochun CHA Univ, Coll Med, Dept Pharmacol, Sungnam 463836, South Korea
关键词
D O I
10.1074/jbc.M509786200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Na+/H+ exchanger 3 (NHE3) plays a pivotal role in transepithelial Na+ and HCO3(+) absorption across a wide range of epithelia in the digestive and renal-genitourinary systems. Accumulating evidence suggests that PDZ-based adaptor proteins play an important role in regulating the trafficking and activity of NHE3. A search for NHE3-binding modular proteins using yeast two-hybrid assays led us to the PDZ-based adaptor Shank2. The interaction between Shank2 and NHE3 was further confirmed by immunoprecipitation and surface plasmon resonance studies. When expressed in PS120/NHE3 cells, Shank2 increased the membrane expression and basal activity of NHE3 and attenuated the cAMP-dependent inhibition of NHE3 activity. Furthermore, knock-down of native Shank2 expression in Caco-2 epithelial cells by RNA interference decreased NHE3 protein expression as well as activity but amplified the inhibitory effect of cAMP on NHE3. These results indicate that Shank2 is a novel NHE3 interacting protein that is involved in the fine regulation of transepithelial salt and water transport through affecting NHE3 expression and activity.
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页码:1461 / 1469
页数:9
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