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Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells
In the animal kingdom, various forms of swarming enable groups of autonomous individuals to transform uncertain information into unified decisions which are probabilistically beneficial. Crossing scales from individual to group decisions requires dynamically accumulating signals among individuals. I...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392205/ https://www.ncbi.nlm.nih.gov/pubmed/32730250 http://dx.doi.org/10.1371/journal.pcbi.1008051 |
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author | Schrom, Edward C. Levin, Simon A. Graham, Andrea L. |
author_facet | Schrom, Edward C. Levin, Simon A. Graham, Andrea L. |
author_sort | Schrom, Edward C. |
collection | PubMed |
description | In the animal kingdom, various forms of swarming enable groups of autonomous individuals to transform uncertain information into unified decisions which are probabilistically beneficial. Crossing scales from individual to group decisions requires dynamically accumulating signals among individuals. In striking parallel, the mammalian immune system is also a group of decentralized autonomous units (i.e. cells) which collectively navigate uncertainty with the help of dynamically accumulating signals (i.e. cytokines). Therefore, we apply techniques of understanding swarm behavior to a decision-making problem in the mammalian immune system, namely effector choice among CD4+ T helper (Th) cells. We find that incorporating dynamic cytokine signaling into a simple model of Th differentiation comprehensively explains divergent observations of this process. The plasticity and heterogeneity of individual Th cells, the tunable mixtures of effector types that can be generated in vitro, and the polarized yet updateable group effector commitment often observed in vivo are all explained by the same set of underlying molecular rules. These rules reveal that Th cells harness dynamic cytokine signaling to implement a system of quorum sensing. Quorum sensing, in turn, may confer adaptive advantages on the mammalian immune system, especially during coinfection and during coevolution with manipulative parasites. This highlights a new way of understanding the mammalian immune system as a cellular swarm, and it underscores the power of collectives throughout nature. |
format | Online Article Text |
id | pubmed-7392205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-73922052020-08-05 Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells Schrom, Edward C. Levin, Simon A. Graham, Andrea L. PLoS Comput Biol Research Article In the animal kingdom, various forms of swarming enable groups of autonomous individuals to transform uncertain information into unified decisions which are probabilistically beneficial. Crossing scales from individual to group decisions requires dynamically accumulating signals among individuals. In striking parallel, the mammalian immune system is also a group of decentralized autonomous units (i.e. cells) which collectively navigate uncertainty with the help of dynamically accumulating signals (i.e. cytokines). Therefore, we apply techniques of understanding swarm behavior to a decision-making problem in the mammalian immune system, namely effector choice among CD4+ T helper (Th) cells. We find that incorporating dynamic cytokine signaling into a simple model of Th differentiation comprehensively explains divergent observations of this process. The plasticity and heterogeneity of individual Th cells, the tunable mixtures of effector types that can be generated in vitro, and the polarized yet updateable group effector commitment often observed in vivo are all explained by the same set of underlying molecular rules. These rules reveal that Th cells harness dynamic cytokine signaling to implement a system of quorum sensing. Quorum sensing, in turn, may confer adaptive advantages on the mammalian immune system, especially during coinfection and during coevolution with manipulative parasites. This highlights a new way of understanding the mammalian immune system as a cellular swarm, and it underscores the power of collectives throughout nature. Public Library of Science 2020-07-30 /pmc/articles/PMC7392205/ /pubmed/32730250 http://dx.doi.org/10.1371/journal.pcbi.1008051 Text en © 2020 Schrom et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Schrom, Edward C. Levin, Simon A. Graham, Andrea L. Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells |
title | Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells |
title_full | Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells |
title_fullStr | Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells |
title_full_unstemmed | Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells |
title_short | Quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper T cells |
title_sort | quorum sensing via dynamic cytokine signaling comprehensively explains divergent patterns of effector choice among helper t cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392205/ https://www.ncbi.nlm.nih.gov/pubmed/32730250 http://dx.doi.org/10.1371/journal.pcbi.1008051 |
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