Javascript must be enabled to continue!
Lysosomal recruitment of TSC2 is a universal response to cellular stress
View through CrossRef
AbstractmTORC1 promotes cell growth and is therefore inactivated upon unfavourable growth conditions. Signalling pathways downstream of most cellular stresses converge on TSC1/2, which serves as an integration point that inhibits mTORC1. The TSC1/2 complex was shown to translocate to lysosomes to inactivate mTORC1 in response to two stresses: amino-acid starvation and growth factor removal. Whether other stresses also regulate TSC2 localization is not known. How TSC2 localization responds to combinations of stresses and other stimuli is also unknown. We show that both amino acids and growth factors are required simultaneously to maintain TSC2 cytoplasmic; when one of the two is missing, TSC2 relocalizes to lysosomes. Furthermore, multiple different stresses that inhibit mTORC1 also drive TSC2 lysosomal accumulation. Our findings indicate that lysosomal recruitment of TSC2 is a universal response to stimuli that inactivate mTORC1, and that the presence of any single stress is sufficient to cause TSC2 lysosomal localization.
Springer Science and Business Media LLC
Title: Lysosomal recruitment of TSC2 is a universal response to cellular stress
Description:
AbstractmTORC1 promotes cell growth and is therefore inactivated upon unfavourable growth conditions.
Signalling pathways downstream of most cellular stresses converge on TSC1/2, which serves as an integration point that inhibits mTORC1.
The TSC1/2 complex was shown to translocate to lysosomes to inactivate mTORC1 in response to two stresses: amino-acid starvation and growth factor removal.
Whether other stresses also regulate TSC2 localization is not known.
How TSC2 localization responds to combinations of stresses and other stimuli is also unknown.
We show that both amino acids and growth factors are required simultaneously to maintain TSC2 cytoplasmic; when one of the two is missing, TSC2 relocalizes to lysosomes.
Furthermore, multiple different stresses that inhibit mTORC1 also drive TSC2 lysosomal accumulation.
Our findings indicate that lysosomal recruitment of TSC2 is a universal response to stimuli that inactivate mTORC1, and that the presence of any single stress is sufficient to cause TSC2 lysosomal localization.
Related Results
Abstract A01: Vps34 promotes macropinocytosis in Tsc2-deficient cells
Abstract A01: Vps34 promotes macropinocytosis in Tsc2-deficient cells
Abstract
Purpose: The mechanistic/mammalian target of rapamycin complex 1 (mTORC1) is constitutively active in many human cancers and in tuberous sclerosis complex (...
Abstract 1721: FOXO1, a downstream substrate of AKT, function as tumor suppressor in HCC carcinogenesis
Abstract 1721: FOXO1, a downstream substrate of AKT, function as tumor suppressor in HCC carcinogenesis
Abstract
Hepatocellular carcinoma (HCC) represents the fifth most common tumor types in the world and the third leading cause of cancer-related death. However, th...
The TSC1-TSC2 complex consists of multiple TSC1 and TSC2 subunits
The TSC1-TSC2 complex consists of multiple TSC1 and TSC2 subunits
Abstract
Background
Mutations to the TSC1 and TSC2 genes cause the disease tuberous sclerosis complex. The TSC1 and TSC2 gene products form a pro...
mTOR signaling and endometrial receptivity in infertile women with intramural uterine leiomyomas
mTOR signaling and endometrial receptivity in infertile women with intramural uterine leiomyomas
Abstract
Background
Receptive endometrium is a restraining factor in the establishment of pregnancy in several estrogen-dependent gynecological diso...
Abstract 5472: Loss of TSC2 function predicts optimal therapeutic response to combinations of MEK and mTOR inhibitors
Abstract 5472: Loss of TSC2 function predicts optimal therapeutic response to combinations of MEK and mTOR inhibitors
Abstract
The MAPK-RAS-PI3K signaling network is oncogenic in many human malignancies. The plasticity of cancer cell ‘circuitry’ is an important consideration in the ...
Vps34-mediated macropinocytosis in Tuberous Sclerosis Complex 2-deficient cells supports tumorigenesis
Vps34-mediated macropinocytosis in Tuberous Sclerosis Complex 2-deficient cells supports tumorigenesis
AbstractTuberous Sclerosis Complex (TSC), a rare genetic disorder with mechanistic target of rapamycin complex 1 (mTORC1) hyperactivation, is characterized by multi-organ hamartoma...
Institutional experience with nab-sirolimus in patients with malignancies harboring TSC1 or TSC2 mutations.
Institutional experience with nab-sirolimus in patients with malignancies harboring TSC1 or TSC2 mutations.
3111 Background: TSC1/ TSC2 genes are tumor suppressors in the mTOR pathway; mutated at low frequency across tumor types (̃1–2%). Retrospective analyses of patients (pts) with mTO...
The deubiquitinase USP32 regulates non-proteolytic ubiquitination in the endosomal-lysosomal system
The deubiquitinase USP32 regulates non-proteolytic ubiquitination in the endosomal-lysosomal system
The regulation of essential cellular processes requires tightly controlled and directed transport of proteins and membranes. The highly dynamic endosomal and lysosomal system forms...

