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Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells

An exclusive feature of dendritic cells (DCs) is their capacity to present exogenous antigens by MHC class I molecules, called cross‐presentation. Here, we show that protein antigen can be conserved in mature murine DCs for several days in a lysosome‐like storage compartment, distinct from MHC class...

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Autores principales: Ho, Nataschja I., Camps, Marcel G., Garcia‐Vallejo, Juan J., Bos, Erik, Koster, Abraham J., Verdoes, Martijn, van Kooyk, Yvette, Ossendorp, Ferry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517591/
https://www.ncbi.nlm.nih.gov/pubmed/34110622
http://dx.doi.org/10.1111/imm.13382
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author Ho, Nataschja I.
Camps, Marcel G.
Garcia‐Vallejo, Juan J.
Bos, Erik
Koster, Abraham J.
Verdoes, Martijn
van Kooyk, Yvette
Ossendorp, Ferry
author_facet Ho, Nataschja I.
Camps, Marcel G.
Garcia‐Vallejo, Juan J.
Bos, Erik
Koster, Abraham J.
Verdoes, Martijn
van Kooyk, Yvette
Ossendorp, Ferry
author_sort Ho, Nataschja I.
collection PubMed
description An exclusive feature of dendritic cells (DCs) is their capacity to present exogenous antigens by MHC class I molecules, called cross‐presentation. Here, we show that protein antigen can be conserved in mature murine DCs for several days in a lysosome‐like storage compartment, distinct from MHC class II and early endosomal compartments, as an internal source for the supply of MHC class I ligands. Using two different uptake routes via Fcγ receptors and C‐type lectin receptors, we could show that antigens were routed towards the same endolysosomal compartments after 48 h. The antigen‐containing compartments lacked co‐expression of molecules involved in MHC class I processing and presentation including TAP and proteasome subunits as shown by single‐cell imaging flow cytometry. Moreover, we observed the absence of cathepsin S but selective co‐localization of active cathepsin X with protein antigen in the storage compartments. This indicates cathepsin S‐independent antigen degradation and a novel but yet undefined role for cathepsin X in antigen processing and cross‐presentation by DCs. In summary, our data suggest that these antigen‐containing compartments in DCs can conserve protein antigens from different uptake routes and contribute to long‐lasting antigen cross‐presentation.
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spelling pubmed-85175912021-10-21 Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells Ho, Nataschja I. Camps, Marcel G. Garcia‐Vallejo, Juan J. Bos, Erik Koster, Abraham J. Verdoes, Martijn van Kooyk, Yvette Ossendorp, Ferry Immunology Original Articles An exclusive feature of dendritic cells (DCs) is their capacity to present exogenous antigens by MHC class I molecules, called cross‐presentation. Here, we show that protein antigen can be conserved in mature murine DCs for several days in a lysosome‐like storage compartment, distinct from MHC class II and early endosomal compartments, as an internal source for the supply of MHC class I ligands. Using two different uptake routes via Fcγ receptors and C‐type lectin receptors, we could show that antigens were routed towards the same endolysosomal compartments after 48 h. The antigen‐containing compartments lacked co‐expression of molecules involved in MHC class I processing and presentation including TAP and proteasome subunits as shown by single‐cell imaging flow cytometry. Moreover, we observed the absence of cathepsin S but selective co‐localization of active cathepsin X with protein antigen in the storage compartments. This indicates cathepsin S‐independent antigen degradation and a novel but yet undefined role for cathepsin X in antigen processing and cross‐presentation by DCs. In summary, our data suggest that these antigen‐containing compartments in DCs can conserve protein antigens from different uptake routes and contribute to long‐lasting antigen cross‐presentation. John Wiley and Sons Inc. 2021-06-30 2021-11 /pmc/articles/PMC8517591/ /pubmed/34110622 http://dx.doi.org/10.1111/imm.13382 Text en © 2021 The Authors. Immunology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Ho, Nataschja I.
Camps, Marcel G.
Garcia‐Vallejo, Juan J.
Bos, Erik
Koster, Abraham J.
Verdoes, Martijn
van Kooyk, Yvette
Ossendorp, Ferry
Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells
title Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells
title_full Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells
title_fullStr Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells
title_full_unstemmed Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells
title_short Distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells
title_sort distinct antigen uptake receptors route to the same storage compartments for cross‐presentation in dendritic cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8517591/
https://www.ncbi.nlm.nih.gov/pubmed/34110622
http://dx.doi.org/10.1111/imm.13382
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