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Patterns, Receptors, and Signals: Regulation of Phagosome Maturation
Recognition of microbial pathogens and dead cells and their phagocytic uptake by specialized immune cells are essential to maintain host homeostasis. Phagosomes undergo fusion and fission events with endosomal and lysosomal compartments, a process called ‘phagosome maturation’, which leads to the de...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455985/ https://www.ncbi.nlm.nih.gov/pubmed/28416446 http://dx.doi.org/10.1016/j.it.2017.03.006 |
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author | Pauwels, Anne-Marie Trost, Matthias Beyaert, Rudi Hoffmann, Eik |
author_facet | Pauwels, Anne-Marie Trost, Matthias Beyaert, Rudi Hoffmann, Eik |
author_sort | Pauwels, Anne-Marie |
collection | PubMed |
description | Recognition of microbial pathogens and dead cells and their phagocytic uptake by specialized immune cells are essential to maintain host homeostasis. Phagosomes undergo fusion and fission events with endosomal and lysosomal compartments, a process called ‘phagosome maturation’, which leads to the degradation of the phagosomal content. However, many phagocytic cells also act as antigen-presenting cells and must balance degradation and peptide preservation. Emerging evidence indicates that receptor engagement by phagosomal cargo, as well as inflammatory mediators and cellular activation affect many aspects of phagosome maturation. Unsurprisingly, pathogens have developed strategies to hijack this machinery, thereby interfering with host immunity. Here, we highlight progress in this field, summarize findings on the impact of immune signals, and discuss consequences for pathogen elimination. |
format | Online Article Text |
id | pubmed-5455985 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54559852017-06-09 Patterns, Receptors, and Signals: Regulation of Phagosome Maturation Pauwels, Anne-Marie Trost, Matthias Beyaert, Rudi Hoffmann, Eik Trends Immunol Review Recognition of microbial pathogens and dead cells and their phagocytic uptake by specialized immune cells are essential to maintain host homeostasis. Phagosomes undergo fusion and fission events with endosomal and lysosomal compartments, a process called ‘phagosome maturation’, which leads to the degradation of the phagosomal content. However, many phagocytic cells also act as antigen-presenting cells and must balance degradation and peptide preservation. Emerging evidence indicates that receptor engagement by phagosomal cargo, as well as inflammatory mediators and cellular activation affect many aspects of phagosome maturation. Unsurprisingly, pathogens have developed strategies to hijack this machinery, thereby interfering with host immunity. Here, we highlight progress in this field, summarize findings on the impact of immune signals, and discuss consequences for pathogen elimination. Elsevier Science Ltd 2017-06 /pmc/articles/PMC5455985/ /pubmed/28416446 http://dx.doi.org/10.1016/j.it.2017.03.006 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Pauwels, Anne-Marie Trost, Matthias Beyaert, Rudi Hoffmann, Eik Patterns, Receptors, and Signals: Regulation of Phagosome Maturation |
title | Patterns, Receptors, and Signals: Regulation of Phagosome Maturation |
title_full | Patterns, Receptors, and Signals: Regulation of Phagosome Maturation |
title_fullStr | Patterns, Receptors, and Signals: Regulation of Phagosome Maturation |
title_full_unstemmed | Patterns, Receptors, and Signals: Regulation of Phagosome Maturation |
title_short | Patterns, Receptors, and Signals: Regulation of Phagosome Maturation |
title_sort | patterns, receptors, and signals: regulation of phagosome maturation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5455985/ https://www.ncbi.nlm.nih.gov/pubmed/28416446 http://dx.doi.org/10.1016/j.it.2017.03.006 |
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