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Developing oligodendrocytes express functional GABABreceptors that stimulate cell proliferation and migration

Authors :
Karen Luyt
Ryuichi Shigemoto
Jienchi J. Dorward
Yue Wu
Claire Durant
Elek Molnár
Timothy P. Slade
Aniko Varadi
Stuart J. Mundell
Source :
Journal of Neurochemistry. 100:822-840
Publication Year :
2007
Publisher :
Wiley, 2007.

Abstract

GABA(B) receptors (GABA(B)Rs) are involved in early events during neuronal development. The presence of GABA(B)Rs in developing oligodendrocytes has not been established. Using immunofluorescent co-localization, we have identified GABA(B)R proteins in O4 marker-positive oligodendrocyte precursor cells (OPCs) in 4-day-old mouse brain periventricular white matter. In culture, OPCs, differentiated oligodendrocytes (DOs) and type 2 astrocytes (ASTs) express both the GABA(B1abcdf) and GABA(B2) subunits of the GABA(B)R. Using semiquantitative PCR analysis with GABA(B)R isoform-selective primers we found that the expression level of GABA(B1abd) was substantially higher in OPCs or ASTs than in DOs. In contrast, the GABA(B2) isoform showed a similar level of expression in OPCs and DOs, and a significantly higher level in ASTs. This indicates that the expression of GABA(B1) and GABA(B2) subunits are under independent control during oligodendroglial development. Activation of GABA(B)Rs using the selective agonist baclofen demonstrated that these receptors are functionally active and negatively coupled to adenylyl cyclase. Manipulation of GABA(B)R activity had no effect on OPC migration in a conventional agarose drop assay, whereas baclofen significantly increased OPC migration in a more sensitive transwell microchamber-based assay. Exposure of cultured OPCs to baclofen increased their proliferation, providing evidence for a functional role of GABA(B)Rs in oligodendrocyte development. The presence of GABA(B)Rs in developing oligodendrocytes provides a new mechanism for neuronal-glial interactions during development and may offer a novel target for promoting remyelination following white matter injury.

Details

ISSN :
14714159 and 00223042
Volume :
100
Database :
OpenAIRE
Journal :
Journal of Neurochemistry
Accession number :
edsair.doi.dedup.....27d6e217762566e06cee3f0851072808
Full Text :
https://doi.org/10.1111/j.1471-4159.2006.04255.x