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Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses
The soil-dwelling social amoeba Dictyostelium discoideum feeds on bacteria. Each meal is a potential infection because some bacteria have evolved mechanisms to resist predation. To survive such a hostile environment, D. discoideum has in turn evolved efficient antimicrobial responses that are intert...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758549/ https://www.ncbi.nlm.nih.gov/pubmed/29354124 http://dx.doi.org/10.3389/fimmu.2017.01906 |
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author | Dunn, Joe Dan Bosmani, Cristina Barisch, Caroline Raykov, Lyudmil Lefrançois, Louise H. Cardenal-Muñoz, Elena López-Jiménez, Ana Teresa Soldati, Thierry |
author_facet | Dunn, Joe Dan Bosmani, Cristina Barisch, Caroline Raykov, Lyudmil Lefrançois, Louise H. Cardenal-Muñoz, Elena López-Jiménez, Ana Teresa Soldati, Thierry |
author_sort | Dunn, Joe Dan |
collection | PubMed |
description | The soil-dwelling social amoeba Dictyostelium discoideum feeds on bacteria. Each meal is a potential infection because some bacteria have evolved mechanisms to resist predation. To survive such a hostile environment, D. discoideum has in turn evolved efficient antimicrobial responses that are intertwined with phagocytosis and autophagy, its nutrient acquisition pathways. The core machinery and antimicrobial functions of these pathways are conserved in the mononuclear phagocytes of mammals, which mediate the initial, innate-immune response to infection. In this review, we discuss the advantages and relevance of D. discoideum as a model phagocyte to study cell-autonomous defenses. We cover the antimicrobial functions of phagocytosis and autophagy and describe the processes that create a microbicidal phagosome: acidification and delivery of lytic enzymes, generation of reactive oxygen species, and the regulation of Zn(2+), Cu(2+), and Fe(2+) availability. High concentrations of metals poison microbes while metal sequestration inhibits their metabolic activity. We also describe microbial interference with these defenses and highlight observations made first in D. discoideum. Finally, we discuss galectins, TNF receptor-associated factors, tripartite motif-containing proteins, and signal transducers and activators of transcription, microbial restriction factors initially characterized in mammalian phagocytes that have either homologs or functional analogs in D. discoideum. |
format | Online Article Text |
id | pubmed-5758549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57585492018-01-19 Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses Dunn, Joe Dan Bosmani, Cristina Barisch, Caroline Raykov, Lyudmil Lefrançois, Louise H. Cardenal-Muñoz, Elena López-Jiménez, Ana Teresa Soldati, Thierry Front Immunol Immunology The soil-dwelling social amoeba Dictyostelium discoideum feeds on bacteria. Each meal is a potential infection because some bacteria have evolved mechanisms to resist predation. To survive such a hostile environment, D. discoideum has in turn evolved efficient antimicrobial responses that are intertwined with phagocytosis and autophagy, its nutrient acquisition pathways. The core machinery and antimicrobial functions of these pathways are conserved in the mononuclear phagocytes of mammals, which mediate the initial, innate-immune response to infection. In this review, we discuss the advantages and relevance of D. discoideum as a model phagocyte to study cell-autonomous defenses. We cover the antimicrobial functions of phagocytosis and autophagy and describe the processes that create a microbicidal phagosome: acidification and delivery of lytic enzymes, generation of reactive oxygen species, and the regulation of Zn(2+), Cu(2+), and Fe(2+) availability. High concentrations of metals poison microbes while metal sequestration inhibits their metabolic activity. We also describe microbial interference with these defenses and highlight observations made first in D. discoideum. Finally, we discuss galectins, TNF receptor-associated factors, tripartite motif-containing proteins, and signal transducers and activators of transcription, microbial restriction factors initially characterized in mammalian phagocytes that have either homologs or functional analogs in D. discoideum. Frontiers Media S.A. 2018-01-04 /pmc/articles/PMC5758549/ /pubmed/29354124 http://dx.doi.org/10.3389/fimmu.2017.01906 Text en Copyright © 2018 Dunn, Bosmani, Barisch, Raykov, Lefrançois, Cardenal-Muñoz, López-Jiménez and Soldati. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Dunn, Joe Dan Bosmani, Cristina Barisch, Caroline Raykov, Lyudmil Lefrançois, Louise H. Cardenal-Muñoz, Elena López-Jiménez, Ana Teresa Soldati, Thierry Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses |
title | Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses |
title_full | Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses |
title_fullStr | Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses |
title_full_unstemmed | Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses |
title_short | Eat Prey, Live: Dictyostelium discoideum As a Model for Cell-Autonomous Defenses |
title_sort | eat prey, live: dictyostelium discoideum as a model for cell-autonomous defenses |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758549/ https://www.ncbi.nlm.nih.gov/pubmed/29354124 http://dx.doi.org/10.3389/fimmu.2017.01906 |
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