Choi Jung Woong, Lee-Kwon Whaseon, Jeon Eun Su, Kang Yong Jung, Kawano Kazuya, Kim Hyeon Soo, Suh Pann-Ghill, Donowitz Mark, Kim Jae Ho
Department of Physiology and Medicine, Gastrointestinal Division, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Biochim Biophys Acta. 2004 Jul 5;1683(1-3):59-68. doi: 10.1016/j.bbalip.2004.04.005.
Lysophosphatidic acid (LPA) stimulates Na(+)/H(+) exchanger 3 (NHE3) activity in opossum kidney proximal tubule (OK) cells by increasing the apical membrane amount of NHE3. This occurs by stimulation of exocytic trafficking of NHE3 to the apical plasma membrane by an E3KARP-dependent mechanism. However, it is still unclear how E3KARP leads to the LPA-induced exocytosis of NHE3. In the current study, we demonstrate that stable expression of exogenous E3KARP increases LPA-induced phospholipase C (PLC) activation and subsequent elevation of intracellular Ca(2+) in opossum kidney proximal tubule (OK) cells. Pretreatment with U73122, a PLC inhibitor, prevented the LPA-induced NHE3 activation and the exocytic trafficking of NHE3. To understand how the elevation of intracellular Ca(2+) leads to the stimulation of NHE3, we pretreated OK cells with BAPTA-AM, an intracellular Ca(2+) chelator. BAPTA-AM completely blocked the LPA-induced increase of NHE3 activity and surface NHE3 amount by decreasing the LPA-induced exocytic trafficking of NHE3. Pretreatment with GF109203X, a PKC inhibitor, did not affect the percent of LPA-induced NHE3 activation and increase of surface NHE3 amount. From these results, we suggest that E3KARP plays a necessary role in LPA-induced PLC activation, and that PLC-dependent elevation of intracellular Ca(2+) but not PKC activation is necessary for the LPA-induced increase of NHE3 exocytosis.
溶血磷脂酸(LPA)通过增加顶端膜上NHE3的量来刺激负鼠肾近端小管(OK)细胞中的Na(+)/H(+)交换体3(NHE3)活性。这是通过一种E3KARP依赖性机制刺激NHE3向顶端质膜的胞吐转运来实现的。然而,E3KARP如何导致LPA诱导的NHE3胞吐作用仍不清楚。在本研究中,我们证明外源性E3KARP的稳定表达增加了LPA诱导的磷脂酶C(PLC)激活以及随后负鼠肾近端小管(OK)细胞内Ca(2+)的升高。用PLC抑制剂U73122预处理可阻止LPA诱导的NHE3激活和NHE3的胞吐转运。为了了解细胞内Ca(2+)的升高如何导致NHE3的刺激,我们用细胞内Ca(2+)螯合剂BAPTA-AM预处理OK细胞。BAPTA-AM通过减少LPA诱导的NHE3胞吐转运,完全阻断了LPA诱导的NHE3活性增加和表面NHE3量的增加。用PKC抑制剂GF109203X预处理不影响LPA诱导的NHE3激活百分比和表面NHE3量的增加。从这些结果中,我们认为E3KARP在LPA诱导的PLC激活中起必要作用,并且LPA诱导的NHE3胞吐增加需要PLC依赖性的细胞内Ca(2+)升高而非PKC激活。