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Criticality of plasma membrane lipids reflects activation state of macrophage cells.

Accepted version
Peer-reviewed

Type

Article

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Authors

Cammarota, Eugenia 
Soriani, Chiara 
Taub, Raphaelle 
Sakai, Jiro 

Abstract

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.

Description

Keywords

critical lipidomics, liquid–liquid phase separation, macrophage activation, plasma membrane composition, Cell Membrane, Macrophages, Membrane Lipids, Membrane Proteins, Protein Transport

Journal Title

J R Soc Interface

Conference Name

Journal ISSN

1742-5689
1742-5662

Volume Title

17

Publisher

The Royal Society

Rights

All rights reserved
Sponsorship
Biotechnology and Biological Sciences Research Council (BB/H021930/1)
Wellcome Trust (108045/Z/15/Z)
Research was funded by EUMarie Curie action ITN TransPol (EC), NIH-R01GM110052 and NSF10 MCB1552439 (SLV), Cambridge University Commonwealth, European and International Trust 11 (JS) ITN BioPol (PC), and Wellcome Trust Investigator grant 08045/Z/15/Z (CEB).