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Autophagy enhances the presentation of endogenous viral antigens on MHC class I molecules during HSV-1 infection.


ABSTRACT: Viral proteins are usually processed by the 'classical' major histocompatibility complex (MHC) class I presentation pathway. Here we showed that although macrophages infected with herpes simplex virus type 1 (HSV-1) initially stimulated CD8(+) T cells by this pathway, a second pathway involving a vacuolar compartment was triggered later during infection. Morphological and functional analyses indicated that distinct forms of autophagy facilitated the presentation of HSV-1 antigens on MHC class I molecules. One form of autophagy involved a previously unknown type of autophagosome that originated from the nuclear envelope. Whereas interferon-gamma stimulated classical MHC class I presentation, fever-like hyperthermia and the pyrogenic cytokine interleukin 1beta activated autophagy and the vacuolar processing of viral peptides. Viral peptides in autophagosomes were further processed by the proteasome, which suggests a complex interaction between the vacuolar and MHC class I presentation pathways.

SUBMITTER: English L 

PROVIDER: S-EPMC3885169 | biostudies-literature | 2009 May

REPOSITORIES: biostudies-literature

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Autophagy enhances the presentation of endogenous viral antigens on MHC class I molecules during HSV-1 infection.

English Luc L   Chemali Magali M   Duron Johanne J   Rondeau Christiane C   Laplante Annie A   Gingras Diane D   Alexander Diane D   Leib David D   Norbury Christopher C   Lippé Roger R   Desjardins Michel M  

Nature immunology 20090322 5


Viral proteins are usually processed by the 'classical' major histocompatibility complex (MHC) class I presentation pathway. Here we showed that although macrophages infected with herpes simplex virus type 1 (HSV-1) initially stimulated CD8(+) T cells by this pathway, a second pathway involving a vacuolar compartment was triggered later during infection. Morphological and functional analyses indicated that distinct forms of autophagy facilitated the presentation of HSV-1 antigens on MHC class I  ...[more]

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