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Dendritic cell maturation and cross‐presentation: timing matters!

As a population, dendritic cells (DCs) appear to be the best cross‐presenters of internalized antigens on major histocompatibility complex class I molecules in the mouse. To do this, DCs have developed a number of unique and dedicated means to control their endocytic and phagocytic pathways: among t...

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Autores principales: Alloatti, Andrés, Kotsias, Fiorella, Magalhaes, Joao Gamelas, Amigorena, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680313/
https://www.ncbi.nlm.nih.gov/pubmed/27319345
http://dx.doi.org/10.1111/imr.12432
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author Alloatti, Andrés
Kotsias, Fiorella
Magalhaes, Joao Gamelas
Amigorena, Sebastian
author_facet Alloatti, Andrés
Kotsias, Fiorella
Magalhaes, Joao Gamelas
Amigorena, Sebastian
author_sort Alloatti, Andrés
collection PubMed
description As a population, dendritic cells (DCs) appear to be the best cross‐presenters of internalized antigens on major histocompatibility complex class I molecules in the mouse. To do this, DCs have developed a number of unique and dedicated means to control their endocytic and phagocytic pathways: among them, the capacity to limit acidification of their phagosomes, to prevent proteolytic degradation, to delay fusion of phagosomes to lysosomes, to recruit ER proteins to phagosomes, and to export phagocytosed antigens to the cytosol. The regulation of phagocytic functions, and thereby of antigen processing and presentation by innate signaling, represents a critical level of integration of adaptive and innate immune responses. Understanding how innate signals control antigen cross‐presentation is critical to define effective vaccination strategies for CD8(+) T‐cell responses.
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spelling pubmed-66803132019-08-09 Dendritic cell maturation and cross‐presentation: timing matters! Alloatti, Andrés Kotsias, Fiorella Magalhaes, Joao Gamelas Amigorena, Sebastian Immunol Rev Invited Reviews As a population, dendritic cells (DCs) appear to be the best cross‐presenters of internalized antigens on major histocompatibility complex class I molecules in the mouse. To do this, DCs have developed a number of unique and dedicated means to control their endocytic and phagocytic pathways: among them, the capacity to limit acidification of their phagosomes, to prevent proteolytic degradation, to delay fusion of phagosomes to lysosomes, to recruit ER proteins to phagosomes, and to export phagocytosed antigens to the cytosol. The regulation of phagocytic functions, and thereby of antigen processing and presentation by innate signaling, represents a critical level of integration of adaptive and innate immune responses. Understanding how innate signals control antigen cross‐presentation is critical to define effective vaccination strategies for CD8(+) T‐cell responses. John Wiley and Sons Inc. 2016-06-20 2016-07 /pmc/articles/PMC6680313/ /pubmed/27319345 http://dx.doi.org/10.1111/imr.12432 Text en © 2016 The Authors. Immunological Reviews Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://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 Invited Reviews
Alloatti, Andrés
Kotsias, Fiorella
Magalhaes, Joao Gamelas
Amigorena, Sebastian
Dendritic cell maturation and cross‐presentation: timing matters!
title Dendritic cell maturation and cross‐presentation: timing matters!
title_full Dendritic cell maturation and cross‐presentation: timing matters!
title_fullStr Dendritic cell maturation and cross‐presentation: timing matters!
title_full_unstemmed Dendritic cell maturation and cross‐presentation: timing matters!
title_short Dendritic cell maturation and cross‐presentation: timing matters!
title_sort dendritic cell maturation and cross‐presentation: timing matters!
topic Invited Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680313/
https://www.ncbi.nlm.nih.gov/pubmed/27319345
http://dx.doi.org/10.1111/imr.12432
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