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Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells

Two transgenic mouse lines expressing an inducible form of the Cre recombinase (CreER(TM)) under the control of the human GFAP promoter have been generated and characterized. In adult mice, expression of the fusion protein is largely confined to astrocytes in all regions of the central nervous syste...

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Autores principales: Chow, Lionel M. L., Zhang, Junyuan, Baker, Suzanne J.
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2522290/
https://www.ncbi.nlm.nih.gov/pubmed/18483774
http://dx.doi.org/10.1007/s11248-008-9185-4
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author Chow, Lionel M. L.
Zhang, Junyuan
Baker, Suzanne J.
author_facet Chow, Lionel M. L.
Zhang, Junyuan
Baker, Suzanne J.
author_sort Chow, Lionel M. L.
collection PubMed
description Two transgenic mouse lines expressing an inducible form of the Cre recombinase (CreER(TM)) under the control of the human GFAP promoter have been generated and characterized. In adult mice, expression of the fusion protein is largely confined to astrocytes in all regions of the central nervous system. Minimal spontaneous Cre activity was detected and recombination was efficiently induced by intraperitoneal administration of tamoxifen in adult mice. The pattern of recombination closely mirrored that of transgene expression. The percentage of astrocytes undergoing recombination varied from region to region ranging from 35% to 70% while a much smaller portion (<1%) of oligodendrocytes and neural precursor cells showed evidence of Cre activity. These mouse lines will provide important tools to dissect gene function in glial cells and in gliomagenesis.
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spelling pubmed-25222902008-08-27 Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells Chow, Lionel M. L. Zhang, Junyuan Baker, Suzanne J. Transgenic Res Original Paper Two transgenic mouse lines expressing an inducible form of the Cre recombinase (CreER(TM)) under the control of the human GFAP promoter have been generated and characterized. In adult mice, expression of the fusion protein is largely confined to astrocytes in all regions of the central nervous system. Minimal spontaneous Cre activity was detected and recombination was efficiently induced by intraperitoneal administration of tamoxifen in adult mice. The pattern of recombination closely mirrored that of transgene expression. The percentage of astrocytes undergoing recombination varied from region to region ranging from 35% to 70% while a much smaller portion (<1%) of oligodendrocytes and neural precursor cells showed evidence of Cre activity. These mouse lines will provide important tools to dissect gene function in glial cells and in gliomagenesis. Springer Netherlands 2008-05-16 2008 /pmc/articles/PMC2522290/ /pubmed/18483774 http://dx.doi.org/10.1007/s11248-008-9185-4 Text en © The Author(s) 2008 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Chow, Lionel M. L.
Zhang, Junyuan
Baker, Suzanne J.
Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells
title Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells
title_full Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells
title_fullStr Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells
title_full_unstemmed Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells
title_short Inducible Cre recombinase activity in mouse mature astrocytes and adult neural precursor cells
title_sort inducible cre recombinase activity in mouse mature astrocytes and adult neural precursor cells
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2522290/
https://www.ncbi.nlm.nih.gov/pubmed/18483774
http://dx.doi.org/10.1007/s11248-008-9185-4
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