NG2-positive cells in the mouse white and grey matter display distinct physiological properties
Cells that express the NG2 proteoglycan are the largest proliferative progenitor population in the postnatal central nervous system (CNS). Although this entire population has long been considered to be oligodendrocyte progenitors, numerous NG2 + cells are present in the cerebral cortex, where relati...
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Published in | The Journal of physiology Vol. 561; no. 1; pp. 109 - 122 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
9600 Garsington Road , Oxford , OX4 2DQ , UK
The Physiological Society
15.11.2004
Blackwell Science Ltd Blackwell Science Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Cells that express the NG2 proteoglycan are the largest proliferative progenitor population in the postnatal central nervous
system (CNS). Although this entire population has long been considered to be oligodendrocyte progenitors, numerous NG2 + cells are present in the cerebral cortex, where relatively little myelination occurs, and also persist long after myelination
is complete in the CNS. Several studies have alluded to the presence of distinct NG2 + cell subtypes based on marker expression, but no experimentally derived hypotheses about the physiological role of these
subtypes has been proposed. In the current study, whole-cell patch-clamp data from acutely isolated slices demonstrate that
subcortical white matter and cortical NG2 + cells display distinct membrane properties in addition to possessing differing K + - and Na + -channel expression profiles. A striking observation is that a subpopulation of cortical, but not white matter NG2 + cells, elicit depolarization-induced spikes that are akin to immature action potentials. Our data demonstrate that a population
of cortical NG2 + cells display physiological properties that differ from their white matter counterparts. |
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Bibliography: | R. Chittajallu and A. Aguirre contributed equally to this work. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0022-3751 1469-7793 |
DOI: | 10.1113/jphysiol.2004.074252 |