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CD46 on glial cells can function as a receptor for viral glycoprotein‐mediated cell–cell fusion

Authors: Riccardo, Cassiani-Ingoni; Heather L, Greenstone; Donatella, Donati; Anna, Fogdell-Hahn; Elena, Martinelli; Daniel, Refai; Roland, Martin; +2 Authors

CD46 on glial cells can function as a receptor for viral glycoprotein‐mediated cell–cell fusion

Abstract

AbstractMembrane cofactor protein (CD46) is a regulator of complement activation that also serves as the entry receptor for human herpes virus 6 (HHV‐6) and measles virus (MV) into human cells. While it is clear that oligodendrocytes and astrocytes are cell types commonly infected by these viruses, it is unclear whether oligodendrocytes express CD46, or which are the cellular mechanisms underlying the infection. We show that adult oligodendrocytes, as well as astrocytes and microglial cells, express CD46 on the cellular surface. Moreover, we employed a quantitative fusion assay to demonstrate that HHV‐6A infection of T lymphocytes enables cell–cell fusion of these cells to astrocytes or to oligodendroglial cells. This fusion is mediated by the interaction between viral glycoproteins expressed on the membrane of the infected cells and CD46 on the glial targets, and is also observed using cells expressing recombinant MV glycoproteins. These data suggest a mechanism that involves cell–cell fusion by which certain viruses could spread the infection from the periphery to the cells in the nervous system. Published 2005 Wiley‐Liss, Inc.

Keywords

Membrane Glycoproteins, Herpesvirus 6, Human, T-Lymphocytes, Brain, Membrane Proteins, Membrane Fusion, Membrane Cofactor Protein, Mice, Oligodendroglia, Astrocytes, Central Nervous System Viral Diseases, NIH 3T3 Cells, Animals, Humans, Capsid Proteins, Neuroglia

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
views
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22
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