Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.

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 intrace...

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Main Authors: Yejie Shi, Hui Yuan, Dong Kim, Vishal Chanana, Akemichi Baba, Toshio Matsuda, Pelin Cengiz, Peter Ferrazzano, Dandan Sun
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3749130?pdf=render
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spelling doaj-49ac93f55e014156b786ee34aeff2fc52020-11-25T01:56:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7420110.1371/journal.pone.0074201Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.Yejie ShiHui YuanDong KimVishal ChananaAkemichi BabaToshio MatsudaPelin CengizPeter FerrazzanoDandan SunRegulation 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 (pHi). 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 Ca(2+) elevation mediated by stimulating reverse mode operation of Na(+)/Ca(2+) 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 Ca(2+) signaling.http://europepmc.org/articles/PMC3749130?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yejie Shi
Hui Yuan
Dong Kim
Vishal Chanana
Akemichi Baba
Toshio Matsuda
Pelin Cengiz
Peter Ferrazzano
Dandan Sun
spellingShingle Yejie Shi
Hui Yuan
Dong Kim
Vishal Chanana
Akemichi Baba
Toshio Matsuda
Pelin Cengiz
Peter Ferrazzano
Dandan Sun
Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.
PLoS ONE
author_facet Yejie Shi
Hui Yuan
Dong Kim
Vishal Chanana
Akemichi Baba
Toshio Matsuda
Pelin Cengiz
Peter Ferrazzano
Dandan Sun
author_sort Yejie Shi
title Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.
title_short Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.
title_full Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.
title_fullStr Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.
title_full_unstemmed Stimulation of Na(+)/H(+) exchanger isoform 1 promotes microglial migration.
title_sort stimulation of na(+)/h(+) exchanger isoform 1 promotes microglial migration.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description 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 (pHi). 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 Ca(2+) elevation mediated by stimulating reverse mode operation of Na(+)/Ca(2+) 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 Ca(2+) signaling.
url http://europepmc.org/articles/PMC3749130?pdf=render
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