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ER-lysosome contacts enable cholesterol sensing by mTORC1 and drive aberrant growth signalling in Niemann-Pick type C.

Chun-Yan Lim | Oliver B Davis | Hijai R Shin | Justin Zhang | Charles A Berdan | Xuntian Jiang | Jessica L Counihan | Daniel S Ory | Daniel K Nomura | Roberto Zoncu
Nature cell biology | 2019

Cholesterol activates the master growth regulator, mTORC1 kinase, by promoting its recruitment to the surface of lysosomes by the Rag guanosine triphosphatases (GTPases). The mechanisms that regulate lysosomal cholesterol content to enable mTORC1 signalling are unknown. Here, we show that oxysterol binding protein (OSBP) and its anchors at the endoplasmic reticulum (ER), VAPA and VAPB, deliver cholesterol across ER-lysosome contacts to activate mTORC1. In cells lacking OSBP, but not other VAP-interacting cholesterol carriers, the recruitment of mTORC1 by the Rag GTPases is inhibited owing to impaired transport of cholesterol to lysosomes. By contrast, OSBP-mediated cholesterol trafficking drives constitutive mTORC1 activation in a disease model caused by the loss of the lysosomal cholesterol transporter, Niemann-Pick C1 (NPC1). Chemical and genetic inactivation of OSBP suppresses aberrant mTORC1 signalling and restores autophagic function in cellular models of Niemann-Pick type C (NPC). Thus, ER-lysosome contacts are signalling hubs that enable cholesterol sensing by mTORC1, and targeting the sterol-transfer activity of these signalling hubs could be beneficial in patients with NPC.

Pubmed ID: 31548609

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: DP2 CA195761
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK056341
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM127763
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL067773

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