Stimulation of Na+/H+ Exchanger Isoform 1 Promotes Microglial Migration

被引:23
作者
Shi, Yejie [1 ,2 ]
Yuan, Hui [1 ]
Kim, Dong [1 ]
Chanana, Vishal [4 ]
Baba, Akemichi [5 ]
Matsuda, Toshio [5 ]
Cengiz, Pelin [4 ]
Ferrazzano, Peter [4 ]
Sun, Dandan [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA
[2] Univ Wisconsin, Neurosci Training Program, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Neurol Surg, Madison, WI USA
[4] Univ Wisconsin, Waisman Ctr, Madison, WI 53705 USA
[5] Osaka Univ, Grad Sch Pharmaceut Sci, Osaka, Japan
来源
PLOS ONE | 2013年 / 8卷 / 08期
基金
美国国家卫生研究院;
关键词
ERM PROTEINS; ACTIN POLYMERIZATION; INCREASED TOLERANCE; IN-VITRO; CELLS; RECEPTORS; CHEMOTAXIS; EXPRESSION; BRADYKININ; GROWTH;
D O I
10.1371/journal.pone.0074201
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Regulation of microglial migration is not well understood. In this study, we proposed that Na+/H+ exchanger isoform 1 (NHE-1) is important in microglial migration. NHE-1 protein was co-localized with cytoskeletal protein ezrin in lamellipodia of microglia and maintained its more alkaline intracellular pH (pH(i)). Chemoattractant bradykinin (BK) stimulated microglial migration by increasing lamellipodial area and protrusion rate, but reducing lamellipodial persistence time. Interestingly, blocking NHE-1 activity with its potent inhibitor HOE 642 not only acidified microglia, abolished the BK-triggered dynamic changes of lamellipodia, but also reduced microglial motility and microchemotaxis in response to BK. In addition, NHE-1 activation resulted in intracellular Na+ loading as well as intracellular Ca2+ elevation mediated by stimulating reverse mode operation of Na+/Ca2+ exchange (NCXrev). Taken together, our study shows that NHE-1 protein is abundantly expressed in microglial lamellipodia and maintains alkaline pHi in response to BK stimulation. In addition, NHE-1 and NCXrev play a concerted role in BK-induced microglial migration via Na+ and Ca2+ signaling.
引用
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页数:17
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