Han WonSun, Kim Kyung Hwan, Jo Min Jae, Lee Ji Hyun, Yang Jinhee, Doctor R Brian, Moe Orson W, Lee Jinu, Kim Eunjoon, Lee Min Goo
Department of Pharmacology, Brain Korea 21 Project for Medical Science, Institute of Gastroenterology, Yonsei University College of Medicine, Seoul 120-752, Korea.
J Biol Chem. 2006 Jan 20;281(3):1461-9. doi: 10.1074/jbc.M509786200. Epub 2005 Nov 17.
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.
钠/氢交换体3(NHE3)在消化系统和肾-泌尿生殖系统的多种上皮细胞跨上皮钠和碳酸氢根(HCO3-)吸收过程中起关键作用。越来越多的证据表明,基于PDZ结构域的衔接蛋白在调节NHE3的转运和活性方面发挥重要作用。利用酵母双杂交实验寻找与NHE3结合的模块化蛋白,使我们发现了基于PDZ结构域的衔接蛋白Shank2。免疫沉淀和表面等离子体共振研究进一步证实了Shank2与NHE3之间的相互作用。当在PS120/NHE3细胞中表达时,Shank2增加了NHE3的膜表达和基础活性,并减弱了cAMP对NHE3活性的抑制作用。此外,通过RNA干扰敲低Caco-2上皮细胞中内源性Shank2的表达,降低了NHE3蛋白的表达和活性,但增强了cAMP对NHE3的抑制作用。这些结果表明,Shank2是一种新型的与NHE3相互作用的蛋白,通过影响NHE3的表达和活性参与跨上皮盐和水转运的精细调节。