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JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain

BACKGROUND: Junctional adhesion molecule-A (JAM-A) is an adhesive protein expressed in various cell types. JAM-A localizes to the tight junctions between contacting endothelial and epithelial cells, where it contributes to cell-cell adhesion and to the control of paracellular permeability. RESULTS:...

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Detalles Bibliográficos
Autores principales: Stelzer, Sandra, Ebnet, Klaus, Schwamborn, Jens C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837050/
https://www.ncbi.nlm.nih.gov/pubmed/20184779
http://dx.doi.org/10.1186/1471-2202-11-27
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author Stelzer, Sandra
Ebnet, Klaus
Schwamborn, Jens C
author_facet Stelzer, Sandra
Ebnet, Klaus
Schwamborn, Jens C
author_sort Stelzer, Sandra
collection PubMed
description BACKGROUND: Junctional adhesion molecule-A (JAM-A) is an adhesive protein expressed in various cell types. JAM-A localizes to the tight junctions between contacting endothelial and epithelial cells, where it contributes to cell-cell adhesion and to the control of paracellular permeability. RESULTS: So far, the expression pattern of JAM-A has not been described in detail for the different cell types of the adult brain. Here we show that a subset of proliferating cells in the adult mouse brain express JAM-A. We further clarify that these cells belong to the lineage of NG2-glia cells. Although these mitotic NG2-glia cells express JAM-A, the protein never shows a polarized subcellular distribution. Also non-mitotic NG2-glia cells express JAM-A in a non-polarized pattern on their surface. CONCLUSIONS: Our data show that JAM-A is a novel surface marker for NG2-glia cells of the adult brain.
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spelling pubmed-28370502010-03-12 JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain Stelzer, Sandra Ebnet, Klaus Schwamborn, Jens C BMC Neurosci Research article BACKGROUND: Junctional adhesion molecule-A (JAM-A) is an adhesive protein expressed in various cell types. JAM-A localizes to the tight junctions between contacting endothelial and epithelial cells, where it contributes to cell-cell adhesion and to the control of paracellular permeability. RESULTS: So far, the expression pattern of JAM-A has not been described in detail for the different cell types of the adult brain. Here we show that a subset of proliferating cells in the adult mouse brain express JAM-A. We further clarify that these cells belong to the lineage of NG2-glia cells. Although these mitotic NG2-glia cells express JAM-A, the protein never shows a polarized subcellular distribution. Also non-mitotic NG2-glia cells express JAM-A in a non-polarized pattern on their surface. CONCLUSIONS: Our data show that JAM-A is a novel surface marker for NG2-glia cells of the adult brain. BioMed Central 2010-02-26 /pmc/articles/PMC2837050/ /pubmed/20184779 http://dx.doi.org/10.1186/1471-2202-11-27 Text en Copyright ©2010 Stelzer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Stelzer, Sandra
Ebnet, Klaus
Schwamborn, Jens C
JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain
title JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain
title_full JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain
title_fullStr JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain
title_full_unstemmed JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain
title_short JAM-A is a novel surface marker for NG2-Glia in the adult mouse brain
title_sort jam-a is a novel surface marker for ng2-glia in the adult mouse brain
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2837050/
https://www.ncbi.nlm.nih.gov/pubmed/20184779
http://dx.doi.org/10.1186/1471-2202-11-27
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