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麻疹病毒经甲醛灭活后,可消除核蛋白依赖CD46向小鼠I类限制性细胞毒性T淋巴细胞的呈递,但对II类限制性辅助性T细胞的呈递无影响。

Formaldehyde inactivation of measles virus abolishes CD46-dependent presentation of nucleoprotein to murine class I-restricted CTLs but not to class II-restricted helper T cells.

作者信息

Cardoso A I, Beauverger P, Gerlier D, Wild T F, Rabourdin-Combe C

机构信息

CNRS, UMR 49, Ecole Normale Supérieure de Lyon, France.

出版信息

Virology. 1995 Sep 10;212(1):255-8. doi: 10.1006/viro.1995.1479.

Abstract

To induce an MHC-restricted specific CTL or Th response, an antigen must be delivered into the appropriate cellular compartment. We explored the role of CD46 in the presentation of measles virus (MV) nucleoprotein (NP) to murine NP-specific and MHC Class I-restricted polyclonal CTLs and the effect of inactivating MV by uv or formaldehyde. CD46(-)- and CD46(+)-transfected murine cells were used as target cells. After MV infection, only the targets which expressed CD46 were lysed by NP-specific class I-restricted CTLs. When MV was uv-inactivated, NP presentation by MHC class I molecules was retained but could be blocked by fusion inhibitors which block virus cell entry. When MV was inactivated with formaldehyde, NP was no longer presented by MHC class I molecules, although it was still presented by MHC class II molecules to a NP-specific class II-restricted T cell hybridoma. These data show that MV binding to the CD46 molecule is a prerequisite for virus-to-cell fusion and that cytosolic delivery of NP is necessary for presentation by class I molecules. Moreover, formaldehyde inactivation of virus induces the loss of class I-restricted presentation of NP due to selective abrogation of fusion and cytosolic delivery of NP.

摘要

为诱导MHC限制的特异性CTL或Th应答,抗原必须被递送至适当的细胞区室。我们探究了CD46在将麻疹病毒(MV)核蛋白(NP)呈递给鼠NP特异性且MHC I类限制的多克隆CTL中的作用,以及紫外线或甲醛使MV失活的影响。用CD46(-)和CD46(+)转染的鼠细胞作为靶细胞。MV感染后,只有表达CD46的靶细胞被NP特异性I类限制的CTL裂解。当MV经紫外线失活后,MHC I类分子对NP的呈递得以保留,但可被阻断病毒进入细胞的融合抑制剂所阻断。当MV用甲醛失活后,NP不再由MHC I类分子呈递,尽管它仍由MHC II类分子呈递给NP特异性II类限制的T细胞杂交瘤。这些数据表明,MV与CD46分子的结合是病毒与细胞融合的先决条件,且NP的胞质递送对于I类分子的呈递是必需的。此外,病毒的甲醛失活导致NP的I类限制呈递丧失,这是由于融合和NP的胞质递送被选择性废除所致。

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