Overexpression of cellular prion protein induces an antioxidant environment altering T cell development in the thymus PrPC AND T CELL DIFFERENTIATION

Cellular prion protein (PrP(C)) is an ubiquitously expressed glycoprotein whose roles are still widely discussed, particularly in the field of immunology. Using TgA20- and Tg33-transgenic mice overexpressing PrP(C), we investigated the consequences of this overexpression on T cell development. In bo...

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Published inThe Journal of immunology (1950) Vol. 176; no. 6; pp. 3490 - 7
Main Authors Jouvin-Marche, Evelyne, Attuil-Audenis, Valérie, Aude-Garcia, Catherine, Rachidi, Walid, Zabel, Mark, Podevin-Dimster, Valérie, Siret, Carole, Huber, Christoph, Martinic, Marianne, Riondel, Jacqueline, Villiers, Christian L., Favier, Alain, Naquet, Philippe, Cesbron, Jean-Yves, Marche, Patrice N.
Format Journal Article
LanguageEnglish
Published Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists 15.03.2006
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Summary:Cellular prion protein (PrP(C)) is an ubiquitously expressed glycoprotein whose roles are still widely discussed, particularly in the field of immunology. Using TgA20- and Tg33-transgenic mice overexpressing PrP(C), we investigated the consequences of this overexpression on T cell development. In both models, overexpression of PrP(C) induces strong alterations at different steps of T cell maturation. On TgA20 mice, we observed that these alterations are cell autonomous and lead to a decrease of alphabeta T cells and a concomitant increase of gammadelta T cell numbers. PrP(C) has been shown to bind and chelate copper and, interestingly, under a copper supplementation diet, TgA20 mice presented a partial restoration of the alphabeta T cell development, suggesting that PrP(C) overexpression, by chelating copper, generates an antioxidant context differentially impacting on alphabeta and gammadelta T cell lineage.
ISSN:0022-1767
1550-6606