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Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice
Oligodendrocytes, the myelinating cells of the central nervous system, orchestrate several key cellular functions in the brain and spinal cord, including axon insulation, energy transfer to neurons, and, eventually, modulation of immune responses. There is growing interest for obtaining reliable mar...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8585802/ https://www.ncbi.nlm.nih.gov/pubmed/33346907 http://dx.doi.org/10.1007/s12031-020-01771-w |
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author | Behrangi, Newshan Lorenz, Peter Kipp, Markus |
author_facet | Behrangi, Newshan Lorenz, Peter Kipp, Markus |
author_sort | Behrangi, Newshan |
collection | PubMed |
description | Oligodendrocytes, the myelinating cells of the central nervous system, orchestrate several key cellular functions in the brain and spinal cord, including axon insulation, energy transfer to neurons, and, eventually, modulation of immune responses. There is growing interest for obtaining reliable markers that can specifically label oligodendroglia and their progeny. In many studies, anti-CC1 antibodies, presumably recognizing the protein adenomatous polyposis coli (APC), are used to label mature, myelinating oligodendrocytes. However, it has been discussed whether anti-CC1 antibodies could recognize as well, under pathological conditions, other cell populations, particularly astrocytes. In this study, we used transgenic mice in which astrocytes are labeled by the enhanced green fluorescent protein (eGFP) under the control of the human glial fibrillary acidic protein (GFAP) promoter. By detailed co-localization studies we were able to demonstrate that a significant proportion of eGFP-expressing cells co-express markers of the oligodendrocyte lineage, such as the transcription factor Oligodendrocyte Transcription Factor 2 (OLIG2); the NG2 proteoglycan, also known as chrondroitin sulfate proteoglycan 4 (CSPG4); or APC. The current finding that the GFAP promoter drives transgene expression in cells of the oligodendrocyte lineage should be considered when interpreting results from co-localization studies. |
format | Online Article Text |
id | pubmed-8585802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-85858022021-11-15 Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice Behrangi, Newshan Lorenz, Peter Kipp, Markus J Mol Neurosci Article Oligodendrocytes, the myelinating cells of the central nervous system, orchestrate several key cellular functions in the brain and spinal cord, including axon insulation, energy transfer to neurons, and, eventually, modulation of immune responses. There is growing interest for obtaining reliable markers that can specifically label oligodendroglia and their progeny. In many studies, anti-CC1 antibodies, presumably recognizing the protein adenomatous polyposis coli (APC), are used to label mature, myelinating oligodendrocytes. However, it has been discussed whether anti-CC1 antibodies could recognize as well, under pathological conditions, other cell populations, particularly astrocytes. In this study, we used transgenic mice in which astrocytes are labeled by the enhanced green fluorescent protein (eGFP) under the control of the human glial fibrillary acidic protein (GFAP) promoter. By detailed co-localization studies we were able to demonstrate that a significant proportion of eGFP-expressing cells co-express markers of the oligodendrocyte lineage, such as the transcription factor Oligodendrocyte Transcription Factor 2 (OLIG2); the NG2 proteoglycan, also known as chrondroitin sulfate proteoglycan 4 (CSPG4); or APC. The current finding that the GFAP promoter drives transgene expression in cells of the oligodendrocyte lineage should be considered when interpreting results from co-localization studies. Springer US 2020-12-21 2021 /pmc/articles/PMC8585802/ /pubmed/33346907 http://dx.doi.org/10.1007/s12031-020-01771-w Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Behrangi, Newshan Lorenz, Peter Kipp, Markus Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice |
title | Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice |
title_full | Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice |
title_fullStr | Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice |
title_full_unstemmed | Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice |
title_short | Oligodendrocyte Lineage Marker Expression in eGFP-GFAP Transgenic Mice |
title_sort | oligodendrocyte lineage marker expression in egfp-gfap transgenic mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8585802/ https://www.ncbi.nlm.nih.gov/pubmed/33346907 http://dx.doi.org/10.1007/s12031-020-01771-w |
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