Department of Molecular Biology, University of Geneva, Geneva, Switzerland.
Department of Biochemistry, University of Geneva, Geneva, Switzerland.
Nat Cell Biol. 2018 Sep;20(9):1043-1051. doi: 10.1038/s41556-018-0150-z. Epub 2018 Aug 27.
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.
雷帕霉素复合物 2(TORC2)的靶标在维持质膜(PM)张力的动态平衡中发挥关键作用。PM 张力增加后 TORC2 的激活涉及 Slm1 和 2 旁系同源物从称为 eisosomes 的 PM 内陷中的再分布到包含 TORC2 的膜隔室。Slm1/2 再定位是如何触发的,以及这是否/如何在 PM 张力降低时在 TORC2 失活中发挥作用尚不清楚。使用渗透压冲击和棕榈酰肉碱作为正交工具来操纵 PM 张力,我们证明 PM 张力的降低会触发预先存在的磷脂酰肌醇-4,5-二磷酸自发地、能量独立地重新形成离散的内陷膜结构域,这些结构域会聚集并使 TORC2 失活。这些结果表明,增加和减少的膜张力是通过不同的机制感知的,突出了膜脂质相分离在机械转导中的作用。