| Literature DB >> 22749019 |
Alejo Efeyan1, Roberto Zoncu, David M Sabatini.
Abstract
The mechanistic target of rapamycin (mTOR) kinase controls growth and metabolism, and its deregulation underlies the pathogenesis of many diseases, including cancer, neurodegeneration, and diabetes. mTOR complex 1 (mTORC1) integrates signals arising from nutrients, energy, and growth factors, but how exactly these signals are propagated await to be fully understood. Recent findings have placed the lysosome, a key mediator of cellular catabolism, at the core of mTORC1 regulation by amino acids. A multiprotein complex that includes the Rag GTPases, Ragulator, and the v-ATPase forms an amino acid-sensing machinery on the lysosomal surface that affects the decision between cell growth and catabolism at multiple levels. The involvement of a catabolic organelle in growth signaling may have important implications for our understanding of mTORC1-related pathologies.Entities:
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Year: 2012 PMID: 22749019 PMCID: PMC3432651 DOI: 10.1016/j.molmed.2012.05.007
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951