Literature DB >> 34785592

Passive coupling of membrane tension and cell volume during active response of cells to osmosis.

Chloé Roffay1, Guillaume Molinard1, Kyoohyun Kim2,3, Marta Urbanska2,3, Virginia Andrade4,5, Victoria Barbarasa1, Paulina Nowak1,6, Vincent Mercier1, José García-Calvo7, Stefan Matile7,8, Robbie Loewith6,8, Arnaud Echard4, Jochen Guck2,3, Martin Lenz9,10, Aurélien Roux11,8.   

Abstract

During osmotic changes of their environment, cells actively regulate their volume and plasma membrane tension that can passively change through osmosis. How tension and volume are coupled during osmotic adaptation remains unknown, as their quantitative characterization is lacking. Here, we performed dynamic membrane tension and cell volume measurements during osmotic shocks. During the first few seconds following the shock, cell volume varied to equilibrate osmotic pressures inside and outside the cell, and membrane tension dynamically followed these changes. A theoretical model based on the passive, reversible unfolding of the membrane as it detaches from the actin cortex during volume increase quantitatively describes our data. After the initial response, tension and volume recovered from hypoosmotic shocks but not from hyperosmotic shocks. Using a fluorescent membrane tension probe (fluorescent lipid tension reporter [Flipper-TR]), we investigated the coupling between tension and volume during these asymmetric recoveries. Caveolae depletion and pharmacological inhibition of ion transporters and channels, mTORCs, and the cytoskeleton all affected tension and volume responses. Treatments targeting mTORC2 and specific downstream effectors caused identical changes to both tension and volume responses, their coupling remaining the same. This supports that the coupling of tension and volume responses to osmotic shocks is primarily regulated by mTORC2.
Copyright © 2021 the Author(s). Published by PNAS.

Entities:  

Keywords:  cell volume; flipper-TR; mechanobiology; osmotic shocks; plasma membrane tension

Mesh:

Substances:

Year:  2021        PMID: 34785592      PMCID: PMC8617515          DOI: 10.1073/pnas.2103228118

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  67 in total

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