Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation

<p>Antigen derived from engulfed apoptotic cells can be cross-presented by dendritic cells (DCs) for the generation of major histocompatibility class I/peptide complexes. While the early events of recognition and internalization of the dying cell have been characterized, the antigen-processing...

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Main Authors: Blachere Nathalie E, Darnell Robert B, Albert Matthew L
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2005-01-01
Series:PLoS Biology
Subjects:
Online Access:http://dx.doi.org/10.1371/journal.pbio.0030185
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spelling doaj-add600e9a7664ef6b2335b239dfda3d92021-07-02T07:16:17ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852005-01-0136e18510.1371/journal.pbio.0030185.20050521Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-PresentationBlachere Nathalie EDarnell Robert BDarnell Robert BAlbert Matthew LAlbert Matthew L<p>Antigen derived from engulfed apoptotic cells can be cross-presented by dendritic cells (DCs) for the generation of major histocompatibility class I/peptide complexes. While the early events of recognition and internalization of the dying cell have been characterized, the antigen-processing pathway or pathways remain unknown. We established a mouse model assaying for the activation of polyclonal T cells reactive to antigen derived from apoptotic cells, and demonstrated two distinct pathways for the trafficking of exogenous epitopes. In the first, exogenous antigen is dependent on the DC's expression of a functional transporter associated with antigen processing (TAP). Surprisingly, we found evidence that a second pathway exists in which transfer of processed antigen from the dying cell allows formation of major histocompatibility class I/peptide complexes in TAP-deficient DCs. In vivo data suggest that in situations of stress (e.g., viral infection), this latter pathway may be more efficient, illustrating that dying cells may preselect immunologically important antigenic determinants.</p> http://dx.doi.org/10.1371/journal.pbio.0030185Immunology
collection DOAJ
language English
format Article
sources DOAJ
author Blachere Nathalie E
Darnell Robert B
Darnell Robert B
Albert Matthew L
Albert Matthew L
spellingShingle Blachere Nathalie E
Darnell Robert B
Darnell Robert B
Albert Matthew L
Albert Matthew L
Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation
PLoS Biology
Immunology
author_facet Blachere Nathalie E
Darnell Robert B
Darnell Robert B
Albert Matthew L
Albert Matthew L
author_sort Blachere Nathalie E
title Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation
title_short Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation
title_full Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation
title_fullStr Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation
title_full_unstemmed Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation
title_sort apoptotic cells deliver processed antigen to dendritic cells for cross-presentation
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2005-01-01
description <p>Antigen derived from engulfed apoptotic cells can be cross-presented by dendritic cells (DCs) for the generation of major histocompatibility class I/peptide complexes. While the early events of recognition and internalization of the dying cell have been characterized, the antigen-processing pathway or pathways remain unknown. We established a mouse model assaying for the activation of polyclonal T cells reactive to antigen derived from apoptotic cells, and demonstrated two distinct pathways for the trafficking of exogenous epitopes. In the first, exogenous antigen is dependent on the DC's expression of a functional transporter associated with antigen processing (TAP). Surprisingly, we found evidence that a second pathway exists in which transfer of processed antigen from the dying cell allows formation of major histocompatibility class I/peptide complexes in TAP-deficient DCs. In vivo data suggest that in situations of stress (e.g., viral infection), this latter pathway may be more efficient, illustrating that dying cells may preselect immunologically important antigenic determinants.</p>
topic Immunology
url http://dx.doi.org/10.1371/journal.pbio.0030185
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