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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...

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Autores principales: Dunn, Joe Dan, Bosmani, Cristina, Barisch, Caroline, Raykov, Lyudmil, Lefrançois, Louise H., Cardenal-Muñoz, Elena, López-Jiménez, Ana Teresa, Soldati, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
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.
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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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