The ectodomain of measles virus envelope glycoprotein does not gain access to the cytosol and MHC class I presentation pathway following virus-cell fusion
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作者:
Cardoso, AI
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机构:ECOLE NORMALE SUPER LYON, CNRS, UMR 49, F-69364 LYON 07, FRANCE
Cardoso, AI
Gerlier, D
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机构:ECOLE NORMALE SUPER LYON, CNRS, UMR 49, F-69364 LYON 07, FRANCE
Gerlier, D
Wild, TF
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机构:ECOLE NORMALE SUPER LYON, CNRS, UMR 49, F-69364 LYON 07, FRANCE
Wild, TF
RabourdinCombe, C
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机构:ECOLE NORMALE SUPER LYON, CNRS, UMR 49, F-69364 LYON 07, FRANCE
RabourdinCombe, C
机构:
[1] ECOLE NORMALE SUPER LYON, CNRS, UMR 49, F-69364 LYON 07, FRANCE
[2] UNIV LYON 1, FAC MED LYON RTH LAENNEC, IVMC, CNRS, UMR 5537, F-69372 LYON 08, FRANCE
[3] INST PASTEUR, INSERM, U404, F-69365 LYON 07, FRANCE
To unravel the intracellular fate of measles virus (MV) haemagglutinin (H) following fusion of the virus envelope with the cell membrane, its presentation by MHC molecules to T cells was explored. After MV infection, murine cells expressing CD46 were lysed by MHC class I-restricted CD8 CTLs specific for the ectodomain of H. In contrast, when sensitized with UV-inactivated MV, they were not lysed by these effecters, but were recognized by H-specific and class Ii-restricted CD4 CTLs. Thus, after MV binding and fusion, H becomes associated with plasma membrane and its ectodomain can reach the endosomal MHC-II but not the cytosolic MHC-I antigen presentation pathway. From these data and a reappraisal of previous reports, it appears that the ectodomains of both MV haemagglutinin fusion proteins, having undergone the fusion step, are not translocated into the cytosol and end up in the endosomes.