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Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF
BACKGROUND: The P-glycoprotein (P-gp), an ATP binding cassette transmembrane transporter, is expressed by astrocytes in the adult brain, and is positively modulated during astrogliosis. In a search for factors involved in this modulation, P-gp overexpression was studied in long-term in vitro astrogl...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2002
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC117802/ https://www.ncbi.nlm.nih.gov/pubmed/12150717 http://dx.doi.org/10.1186/1471-2121-3-20 |
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author | Monville, Christelle Fages, Christiane Feyens, Anne-Marie d'Hondt, Véronique Guillet, Catherine Vernallis, Ann Gascan, Hugues Peschanski, Marc |
author_facet | Monville, Christelle Fages, Christiane Feyens, Anne-Marie d'Hondt, Véronique Guillet, Catherine Vernallis, Ann Gascan, Hugues Peschanski, Marc |
author_sort | Monville, Christelle |
collection | PubMed |
description | BACKGROUND: The P-glycoprotein (P-gp), an ATP binding cassette transmembrane transporter, is expressed by astrocytes in the adult brain, and is positively modulated during astrogliosis. In a search for factors involved in this modulation, P-gp overexpression was studied in long-term in vitro astroglial cultures. RESULTS: Surprisingly, most factors that are known to induce astroglial activation in astroglial cultures failed to increase P-gp expression. The only effective proteins were IFNγ and those belonging to the IL-6 family of cytokines (IL-6, LIF, CT-1 and CNTF). As well as P-gp expression, the IL-6 type cytokines - but not IFNγ - stimulated the expression of endogenous CNTF in astrocytes. In order to see whether an increased intracellular level of CNTF was necessary for induction of P-gp overexpression by IL-6 type cytokines, by the same cytokines analysis was carried out on astrocytes obtained from CNTF knockout mice. In these conditions, IFNγ produced increased P-gp expression, but no overexpression of P-gp was observed with either IL-6, LIF or CT-1, pointing to a role of CNTF in the intracellular signalling pathway leading to P-gp overexpression. In agreement with this suggestion, application of exogenous CNTF -which is internalised with its receptor - produced an overexpression of P-gp in CNTF-deficient astrocytes. CONCLUSIONS: These results reveal two different pathways regulating P-gp expression and activity in reactive astrocytes, one of which depends upon the intracellular concentration of CNTF. This regulation of P-gp may be one of the long searched for physiological roles of CNTF. |
format | Text |
id | pubmed-117802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1178022002-08-15 Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF Monville, Christelle Fages, Christiane Feyens, Anne-Marie d'Hondt, Véronique Guillet, Catherine Vernallis, Ann Gascan, Hugues Peschanski, Marc BMC Cell Biol Research Article BACKGROUND: The P-glycoprotein (P-gp), an ATP binding cassette transmembrane transporter, is expressed by astrocytes in the adult brain, and is positively modulated during astrogliosis. In a search for factors involved in this modulation, P-gp overexpression was studied in long-term in vitro astroglial cultures. RESULTS: Surprisingly, most factors that are known to induce astroglial activation in astroglial cultures failed to increase P-gp expression. The only effective proteins were IFNγ and those belonging to the IL-6 family of cytokines (IL-6, LIF, CT-1 and CNTF). As well as P-gp expression, the IL-6 type cytokines - but not IFNγ - stimulated the expression of endogenous CNTF in astrocytes. In order to see whether an increased intracellular level of CNTF was necessary for induction of P-gp overexpression by IL-6 type cytokines, by the same cytokines analysis was carried out on astrocytes obtained from CNTF knockout mice. In these conditions, IFNγ produced increased P-gp expression, but no overexpression of P-gp was observed with either IL-6, LIF or CT-1, pointing to a role of CNTF in the intracellular signalling pathway leading to P-gp overexpression. In agreement with this suggestion, application of exogenous CNTF -which is internalised with its receptor - produced an overexpression of P-gp in CNTF-deficient astrocytes. CONCLUSIONS: These results reveal two different pathways regulating P-gp expression and activity in reactive astrocytes, one of which depends upon the intracellular concentration of CNTF. This regulation of P-gp may be one of the long searched for physiological roles of CNTF. BioMed Central 2002-07-31 /pmc/articles/PMC117802/ /pubmed/12150717 http://dx.doi.org/10.1186/1471-2121-3-20 Text en Copyright © 2002 Monville et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Monville, Christelle Fages, Christiane Feyens, Anne-Marie d'Hondt, Véronique Guillet, Catherine Vernallis, Ann Gascan, Hugues Peschanski, Marc Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF |
title | Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF |
title_full | Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF |
title_fullStr | Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF |
title_full_unstemmed | Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF |
title_short | Astroglial expression of the P-glycoprotein is controlled by intracellular CNTF |
title_sort | astroglial expression of the p-glycoprotein is controlled by intracellular cntf |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC117802/ https://www.ncbi.nlm.nih.gov/pubmed/12150717 http://dx.doi.org/10.1186/1471-2121-3-20 |
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