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酸敏感离子通道蛋白调节平滑肌细胞迁移。

ASIC proteins regulate smooth muscle cell migration.

作者信息

Grifoni Samira C, Jernigan Nikki L, Hamilton Gina, Drummond Heather A

机构信息

Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, MS 39216, USA.

出版信息

Microvasc Res. 2008 Mar;75(2):202-10. doi: 10.1016/j.mvr.2007.08.003. Epub 2007 Aug 25.

Abstract

The purpose of the present study was to investigate Acid Sensing Ion Channel (ASIC) protein expression and importance in cellular migration. We recently demonstrated that Epithelial Na(+)Channel (ENaC) proteins are required for vascular smooth muscle cell (VSMC) migration; however, the role of the closely related ASIC proteins has not been addressed. We used RT-PCR and immunolabeling to determine expression of ASIC1, ASIC2, ASIC3 and ASIC4 in A10 cells. We used small interference RNA to silence individual ASIC expression and determine the importance of ASIC proteins in wound healing and chemotaxis (PDGF-bb)-initiated migration. We found ASIC1, ASIC2, and ASIC3, but not ASIC4, expression in A10 cells. ASIC1, ASIC2, and ASIC3 siRNA molecules significantly suppressed expression of their respective proteins compared to non-targeting siRNA (RISC) transfected controls by 63%, 44%, and 55%, respectively. Wound healing was inhibited by 10, 20, and 26% compared to RISC controls following suppression of ASIC1, ASIC2, and ASIC3, respectively. Chemotactic migration was inhibited by 30% and 45%, respectively, following suppression of ASIC1 and ASIC3. ASIC2 suppression produced a small, but significant, increase in chemotactic migration (4%). Our data indicate that ASIC expression is required for normal migration and may suggest a novel role for ASIC proteins in cellular migration.

摘要

本研究的目的是调查酸敏感离子通道(ASIC)蛋白的表达及其在细胞迁移中的重要性。我们最近证明,血管平滑肌细胞(VSMC)迁移需要上皮钠通道(ENaC)蛋白;然而,与之密切相关的ASIC蛋白的作用尚未得到研究。我们使用逆转录聚合酶链反应(RT-PCR)和免疫标记法来确定A10细胞中ASIC1、ASIC2、ASIC3和ASIC4的表达。我们使用小干扰RNA沉默单个ASIC的表达,并确定ASIC蛋白在伤口愈合和趋化性(血小板衍生生长因子-bb,PDGF-bb)引发的迁移中的重要性。我们发现A10细胞中存在ASIC1、ASIC2和ASIC3的表达,但不存在ASIC4的表达。与非靶向小干扰RNA(RNA诱导沉默复合体,RISC)转染的对照相比,ASIC1、ASIC2和ASIC3的小干扰RNA分子分别显著抑制了其各自蛋白的表达,抑制率分别为63%、44%和55%。在分别抑制ASIC1、ASIC2和ASIC3后,与RISC对照相比,伤口愈合分别受到10%、20%和26%的抑制。在抑制ASIC1和ASIC3后,趋化性迁移分别受到30%和45%的抑制。抑制ASIC2会使趋化性迁移出现小幅但显著的增加(4%)。我们的数据表明,正常迁移需要ASIC的表达,这可能提示ASIC蛋白在细胞迁移中具有新的作用。

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