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Glycosylation-related genes are variably expressed depending on the differentiation state of a bioaminergic neuronal cell line: implication for the cellular prion protein

Authors :
Daniel Petit
Odile Kellermann
Aurélien Le Duc
Myriam Ermonval
Paul-François Gallet
Différentiation cellulaire, cellules souches et prions
Institut Pasteur [Paris]
FRE 2937
Centre National de la Recherche Scientifique (CNRS)
Génétique Moléculaire des Bunyavirus
Unité de Génétique Moléculaire Animale (UMR GMA)
Université de Limoges (UNILIM)-Institut National de la Recherche Agronomique (INRA)
This work was supported by the 'Conseil Régional du Limousin' and by 'INRA' (Institut National de la Recherche Agronomique), 'CNRS' and 'Institut Pasteur' and by grants from 'GIS Infection à Prion'.
Unité de Génétique Moléculaire Animale (UGMA)
Institut Pasteur [Paris] (IP)
Source :
Glycoconjugate Journal, Glycoconjugate Journal, Springer Verlag, 2009, 26 (4), pp.477-493. ⟨10.1007/s10719-008-9198-5⟩, Glycoconjugate Journal, 2009, 26 (4), pp.477-493. ⟨10.1007/s10719-008-9198-5⟩
Publication Year :
2008
Publisher :
Springer Science and Business Media LLC, 2008.

Abstract

Chantier qualité GA; A striking feature of the cellular prion protein (PrPC) is the heterogeneity of its glycoforms, whose contribution to PrPC function has yet to be defined. Using the 1C11 neuronal bioaminergic differentiation model and a glycomics approach, we show here a correlation between differential PrPC N-glycosylations in 1C115-HT serotonergic and 1C11NE noradrenergic cells compared to their 1C11 precursor cells and a variation of the glycogenome expression status in these cells. In particular, expression of genes involved in N-glycan synthesis or in the modeling of chondroitin and heparan sulfate proteoglycans appeared to be modulated. Our results highlight that, the expression of glycosylation-related genes is regulated during bioaminergic neuronal differentiation, consistent with a participation of glycoconjugates in neuronal development and plasticity. A neuronal regulation of glycosylation processes may have direct implications on some neurospecific functions of PrPC and may participate in specific brain targeting of prion strains.

Details

ISSN :
15734986 and 02820080
Volume :
26
Database :
OpenAIRE
Journal :
Glycoconjugate Journal
Accession number :
edsair.doi.dedup.....4657627611a94df9f5d2cc1dbcc94204