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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.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
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