Cargando…

Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2

The Target of Rapamycin Complex 2 (TORC2) plays a key role in maintaining the homeostasis of plasma membrane (PM) tension. TORC2 activation upon increased PM tension involves redistribution of the Slm1 and 2 paralogs from PM invaginations known as eisosomes into membrane compartments containing TORC...

Descripción completa

Detalles Bibliográficos
Autores principales: Riggi, Margot, Niewola-Staszkowska, Karolina, Chiaruttini, Nicolas, Colom, Adai, Kusmider, Beata, Mercier, Vincent, Soleimanpour, Saeideh, Stahl, Michael, Matile, Stefan, Roux, Aurélien, Loewith, Robbie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237274/
https://www.ncbi.nlm.nih.gov/pubmed/30154550
http://dx.doi.org/10.1038/s41556-018-0150-z
_version_ 1783371163082162176
author Riggi, Margot
Niewola-Staszkowska, Karolina
Chiaruttini, Nicolas
Colom, Adai
Kusmider, Beata
Mercier, Vincent
Soleimanpour, Saeideh
Stahl, Michael
Matile, Stefan
Roux, Aurélien
Loewith, Robbie
author_facet Riggi, Margot
Niewola-Staszkowska, Karolina
Chiaruttini, Nicolas
Colom, Adai
Kusmider, Beata
Mercier, Vincent
Soleimanpour, Saeideh
Stahl, Michael
Matile, Stefan
Roux, Aurélien
Loewith, Robbie
author_sort Riggi, Margot
collection PubMed
description The Target of Rapamycin Complex 2 (TORC2) plays a key role in maintaining the homeostasis of plasma membrane (PM) tension. TORC2 activation upon increased PM tension involves redistribution of the Slm1 and 2 paralogs from PM invaginations known as eisosomes into membrane compartments containing TORC2. How Slm1/2 relocalization is triggered, and if/how this plays a role in TORC2 inactivation upon decreased PM tension is unknown. Using osmotic shocks and Palmitoylcarnitine (PalmC) as orthogonal tools to manipulate PM tension, we demonstrate that decreased PM tension triggers spontaneous, energy-independent reorganization of pre-existing phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P(2)) into discrete invaginated membrane domains which cluster and inactivate TORC2. These results demonstrate that an increase and a decrease in membrane tension are sensed through different mechanisms and highlight a role for membrane lipid phase separation in mechanotransduction.
format Online
Article
Text
id pubmed-6237274
institution National Center for Biotechnology Information
language English
publishDate 2018
record_format MEDLINE/PubMed
spelling pubmed-62372742019-02-27 Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2 Riggi, Margot Niewola-Staszkowska, Karolina Chiaruttini, Nicolas Colom, Adai Kusmider, Beata Mercier, Vincent Soleimanpour, Saeideh Stahl, Michael Matile, Stefan Roux, Aurélien Loewith, Robbie Nat Cell Biol Article The Target of Rapamycin Complex 2 (TORC2) plays a key role in maintaining the homeostasis of plasma membrane (PM) tension. TORC2 activation upon increased PM tension involves redistribution of the Slm1 and 2 paralogs from PM invaginations known as eisosomes into membrane compartments containing TORC2. How Slm1/2 relocalization is triggered, and if/how this plays a role in TORC2 inactivation upon decreased PM tension is unknown. Using osmotic shocks and Palmitoylcarnitine (PalmC) as orthogonal tools to manipulate PM tension, we demonstrate that decreased PM tension triggers spontaneous, energy-independent reorganization of pre-existing phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P(2)) into discrete invaginated membrane domains which cluster and inactivate TORC2. These results demonstrate that an increase and a decrease in membrane tension are sensed through different mechanisms and highlight a role for membrane lipid phase separation in mechanotransduction. 2018-08-27 2018-09 /pmc/articles/PMC6237274/ /pubmed/30154550 http://dx.doi.org/10.1038/s41556-018-0150-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Riggi, Margot
Niewola-Staszkowska, Karolina
Chiaruttini, Nicolas
Colom, Adai
Kusmider, Beata
Mercier, Vincent
Soleimanpour, Saeideh
Stahl, Michael
Matile, Stefan
Roux, Aurélien
Loewith, Robbie
Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2
title Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2
title_full Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2
title_fullStr Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2
title_full_unstemmed Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2
title_short Decrease in Plasma Membrane Tension Triggers PtdIns(4,5)P(2) Phase Separation to Inactivate TORC2
title_sort decrease in plasma membrane tension triggers ptdins(4,5)p(2) phase separation to inactivate torc2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6237274/
https://www.ncbi.nlm.nih.gov/pubmed/30154550
http://dx.doi.org/10.1038/s41556-018-0150-z
work_keys_str_mv AT riggimargot decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT niewolastaszkowskakarolina decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT chiaruttininicolas decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT colomadai decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT kusmiderbeata decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT merciervincent decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT soleimanpoursaeideh decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT stahlmichael decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT matilestefan decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT rouxaurelien decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2
AT loewithrobbie decreaseinplasmamembranetensiontriggersptdins45p2phaseseparationtoinactivatetorc2