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Criticality of plasma membrane lipids reflects activation state of macrophage cells
Signalling is of particular importance in immune cells, and upstream in the signalling pathway many membrane receptors are functional only as complexes, co-locating with particular lipid species. Work over the last 15 years has shown that plasma membrane lipid composition is close to a critical poin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061703/ https://www.ncbi.nlm.nih.gov/pubmed/32019470 http://dx.doi.org/10.1098/rsif.2019.0803 |
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author | Cammarota, Eugenia Soriani, Chiara Taub, Raphaelle Morgan, Fiona Sakai, Jiro Veatch, Sarah L. Bryant, Clare E. Cicuta, Pietro |
author_facet | Cammarota, Eugenia Soriani, Chiara Taub, Raphaelle Morgan, Fiona Sakai, Jiro Veatch, Sarah L. Bryant, Clare E. Cicuta, Pietro |
author_sort | Cammarota, Eugenia |
collection | PubMed |
description | Signalling is of particular importance in immune cells, and upstream in the signalling pathway many membrane receptors are functional only as complexes, co-locating with particular lipid species. Work over the last 15 years has shown that plasma membrane lipid composition is close to a critical point of phase separation, with evidence that cells adapt their composition in ways that alter the proximity to this thermodynamic point. Macrophage cells are a key component of the innate immune system, are responsive to infections and regulate the local state of inflammation. We investigate changes in the plasma membrane’s proximity to the critical point as a response to stimulation by various pro- and anti-inflammatory agents. Pro-inflammatory (interferon γ, Kdo 2-Lipid A, lipopolysaccharide) perturbations induce an increase in the transition temperature of giant plasma membrane vesicles; anti-inflammatory interleukin 4 has the opposite effect. These changes recapitulate complex plasma membrane composition changes, and are consistent with lipid criticality playing a master regulatory role: being closer to critical conditions increases membrane protein activity. |
format | Online Article Text |
id | pubmed-7061703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70617032020-03-26 Criticality of plasma membrane lipids reflects activation state of macrophage cells Cammarota, Eugenia Soriani, Chiara Taub, Raphaelle Morgan, Fiona Sakai, Jiro Veatch, Sarah L. Bryant, Clare E. Cicuta, Pietro J R Soc Interface Life Sciences–Physics interface Signalling is of particular importance in immune cells, and upstream in the signalling pathway many membrane receptors are functional only as complexes, co-locating with particular lipid species. Work over the last 15 years has shown that plasma membrane lipid composition is close to a critical point of phase separation, with evidence that cells adapt their composition in ways that alter the proximity to this thermodynamic point. Macrophage cells are a key component of the innate immune system, are responsive to infections and regulate the local state of inflammation. We investigate changes in the plasma membrane’s proximity to the critical point as a response to stimulation by various pro- and anti-inflammatory agents. Pro-inflammatory (interferon γ, Kdo 2-Lipid A, lipopolysaccharide) perturbations induce an increase in the transition temperature of giant plasma membrane vesicles; anti-inflammatory interleukin 4 has the opposite effect. These changes recapitulate complex plasma membrane composition changes, and are consistent with lipid criticality playing a master regulatory role: being closer to critical conditions increases membrane protein activity. The Royal Society 2020-02 2020-02-05 /pmc/articles/PMC7061703/ /pubmed/32019470 http://dx.doi.org/10.1098/rsif.2019.0803 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Physics interface Cammarota, Eugenia Soriani, Chiara Taub, Raphaelle Morgan, Fiona Sakai, Jiro Veatch, Sarah L. Bryant, Clare E. Cicuta, Pietro Criticality of plasma membrane lipids reflects activation state of macrophage cells |
title | Criticality of plasma membrane lipids reflects activation state of macrophage cells |
title_full | Criticality of plasma membrane lipids reflects activation state of macrophage cells |
title_fullStr | Criticality of plasma membrane lipids reflects activation state of macrophage cells |
title_full_unstemmed | Criticality of plasma membrane lipids reflects activation state of macrophage cells |
title_short | Criticality of plasma membrane lipids reflects activation state of macrophage cells |
title_sort | criticality of plasma membrane lipids reflects activation state of macrophage cells |
topic | Life Sciences–Physics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7061703/ https://www.ncbi.nlm.nih.gov/pubmed/32019470 http://dx.doi.org/10.1098/rsif.2019.0803 |
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