Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.

Axon remyelination in the central nervous system requires oligodendrocytes that produce myelin. Failure of this repair process is characteristic of neurodegeneration in demyelinating diseases such as multiple sclerosis, and it remains unclear how the lesion microenvironment contributes to decreased...

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Main Authors: Anna Jagielska, Kristen D Wilhite, Krystyn J Van Vliet
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3786906?pdf=render
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spelling doaj-0c11105276d0416c86283fe646d5e7c12020-11-24T21:16:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7604810.1371/journal.pone.0076048Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.Anna JagielskaKristen D WilhiteKrystyn J Van VlietAxon remyelination in the central nervous system requires oligodendrocytes that produce myelin. Failure of this repair process is characteristic of neurodegeneration in demyelinating diseases such as multiple sclerosis, and it remains unclear how the lesion microenvironment contributes to decreased remyelination potential of oligodendrocytes. Here, we show that acidic extracellular pH, which is characteristic of demyelinating lesions, decreases the migration, proliferation, and survival of oligodendrocyte precursor cells (OPCs), and reduces their differentiation into oligodendrocytes. Further, OPCs exhibit directional migration along pH gradients toward acidic pH. These in vitro findings support a possible in vivo scenario whereby pH gradients attract OPCs toward acidic lesions, but resulting reduction in OPC survival and motility in acid decreases progress toward demyelinated axons and is further compounded by decreased differentiation into myelin-producing oligodendrocytes. As these processes are integral to OPC response to nerve demyelination, our results suggest that lesion acidity could contribute to decreased remyelination.http://europepmc.org/articles/PMC3786906?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Anna Jagielska
Kristen D Wilhite
Krystyn J Van Vliet
spellingShingle Anna Jagielska
Kristen D Wilhite
Krystyn J Van Vliet
Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.
PLoS ONE
author_facet Anna Jagielska
Kristen D Wilhite
Krystyn J Van Vliet
author_sort Anna Jagielska
title Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.
title_short Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.
title_full Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.
title_fullStr Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.
title_full_unstemmed Extracellular acidic pH inhibits oligodendrocyte precursor viability, migration, and differentiation.
title_sort extracellular acidic ph inhibits oligodendrocyte precursor viability, migration, and differentiation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Axon remyelination in the central nervous system requires oligodendrocytes that produce myelin. Failure of this repair process is characteristic of neurodegeneration in demyelinating diseases such as multiple sclerosis, and it remains unclear how the lesion microenvironment contributes to decreased remyelination potential of oligodendrocytes. Here, we show that acidic extracellular pH, which is characteristic of demyelinating lesions, decreases the migration, proliferation, and survival of oligodendrocyte precursor cells (OPCs), and reduces their differentiation into oligodendrocytes. Further, OPCs exhibit directional migration along pH gradients toward acidic pH. These in vitro findings support a possible in vivo scenario whereby pH gradients attract OPCs toward acidic lesions, but resulting reduction in OPC survival and motility in acid decreases progress toward demyelinated axons and is further compounded by decreased differentiation into myelin-producing oligodendrocytes. As these processes are integral to OPC response to nerve demyelination, our results suggest that lesion acidity could contribute to decreased remyelination.
url http://europepmc.org/articles/PMC3786906?pdf=render
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AT kristendwilhite extracellularacidicphinhibitsoligodendrocyteprecursorviabilitymigrationanddifferentiation
AT krystynjvanvliet extracellularacidicphinhibitsoligodendrocyteprecursorviabilitymigrationanddifferentiation
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