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Decrease in plasma membrane tension triggers PtdIns(4,5)P2 phase separation to inactivate TORC2.


ABSTRACT: The target of rapamycin complex 2 (TORC2) plays a key role in maintaining the homeostasis of plasma membrane (PM) tension. TORC2 activation following increased PM tension involves redistribution of the Slm1 and 2 paralogues 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 with decreased PM tension, is unknown. Using osmotic shocks and palmitoylcarnitine 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 into discrete invaginated membrane domains, which cluster and inactivate TORC2. These results demonstrate that increased and decreased membrane tension are sensed through different mechanisms, highlighting a role for membrane lipid phase separation in mechanotransduction.

SUBMITTER: Riggi M 

PROVIDER: S-EPMC6237274 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

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Decrease in plasma membrane tension triggers PtdIns(4,5)P<sub>2</sub> phase separation to inactivate TORC2.

Riggi Margot M   Niewola-Staszkowska Karolina K   Chiaruttini Nicolas N   Colom Adai A   Kusmider Beata B   Mercier Vincent V   Soleimanpour Saeideh S   Stahl Michael M   Matile Stefan S   Roux Aurélien A   Loewith Robbie R  

Nature cell biology 20180827 9


The target of rapamycin complex 2 (TORC2) plays a key role in maintaining the homeostasis of plasma membrane (PM) tension. TORC2 activation following increased PM tension involves redistribution of the Slm1 and 2 paralogues 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 with decreased PM tension, is unknown. Using osmotic shocks and palmitoylcarnitine as orthogonal to  ...[more]

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