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神经胶质细胞上的CD46可作为病毒糖蛋白介导的细胞间融合的受体。

CD46 on glial cells can function as a receptor for viral glycoprotein-mediated cell-cell fusion.

作者信息

Cassiani-Ingoni Riccardo, Greenstone Heather L, Donati Donatella, Fogdell-Hahn Anna, Martinelli Elena, Refai Daniel, Martin Roland, Berger Edward A, Jacobson Steven

机构信息

Neuroimmunology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Glia. 2005 Nov 15;52(3):252-8. doi: 10.1002/glia.20219.

Abstract

Membrane 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.

摘要

膜辅因子蛋白(CD46)是补体激活的调节剂,同时也是人类疱疹病毒6型(HHV-6)和麻疹病毒(MV)进入人类细胞的进入受体。虽然很明显少突胶质细胞和星形胶质细胞是这些病毒常见感染的细胞类型,但尚不清楚少突胶质细胞是否表达CD46,以及感染背后的细胞机制是什么。我们发现成年少突胶质细胞以及星形胶质细胞和小胶质细胞在细胞表面表达CD46。此外,我们采用定量融合试验证明,HHV-6A感染T淋巴细胞可使这些细胞与星形胶质细胞或少突胶质细胞发生细胞间融合。这种融合是由感染细胞表面表达的病毒糖蛋白与胶质靶细胞上的CD46之间的相互作用介导的,使用表达重组MV糖蛋白的细胞也可观察到这种融合。这些数据提示了一种涉及细胞间融合的机制,某些病毒可能通过这种机制将感染从外周传播到神经系统中的细胞。

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