{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T00:39:26Z","timestamp":1793320766104,"version":"4.5.0"},"reference-count":45,"publisher":"American Association for the Advancement of Science (AAAS)","issue":"724","content-domain":{"domain":["www.science.org"],"crossmark-restriction":true},"short-container-title":["Sci. Transl. Med."],"published-print":{"date-parts":[[2023,11,29]]},"abstract":"<jats:p>\n                    Pathologic \u03b1-synuclein plays an important role in the pathogenesis of \u03b1-synucleinopathies such as Parkinson\u2019s disease (PD). Disruption of proteostasis is thought to be central to pathologic \u03b1-synuclein toxicity; however, the molecular mechanism of this deregulation is poorly understood. Complementary proteomic approaches in cellular and animal models of PD were used to identify and characterize the pathologic \u03b1-synuclein interactome. We report that the highest biological processes that interacted with pathologic \u03b1-synuclein in mice included RNA processing and translation initiation. Regulation of catabolic processes that include autophagy were also identified. Pathologic \u03b1-synuclein was found to bind with the tuberous sclerosis protein 2 (TSC2) and to trigger the activation of the mammalian target of rapamycin (mTOR) complex 1 (mTORC1), which augmented mRNA translation and protein synthesis, leading to neurodegeneration. Genetic and pharmacologic inhibition of mTOR and protein synthesis rescued the dopamine neuron loss, behavioral deficits, and aberrant biochemical signaling in the \u03b1-synuclein preformed fibril mouse model and\n                    <jats:italic>Drosophila<\/jats:italic>\n                    transgenic models of pathologic \u03b1-synuclein\u2013induced degeneration. Pathologic \u03b1-synuclein furthermore led to a destabilization of the TSC1-TSC2 complex, which plays an important role in mTORC1 activity. Constitutive overexpression of TSC2 rescued motor deficits and neuropathology in \u03b1-synuclein flies. Biochemical examination of PD postmortem brain tissues also suggested deregulated mTORC1 signaling. These findings establish a connection between mRNA translation deregulation and mTORC1 pathway activation that is induced by pathologic \u03b1-synuclein in cellular and animal models of PD.\n                  <\/jats:p>","DOI":"10.1126\/scitranslmed.add0499","type":"journal-article","created":{"date-parts":[[2023,11,29]],"date-time":"2023-11-29T13:59:02Z","timestamp":1701266342000},"update-policy":"https:\/\/doi.org\/10.34133\/aaas_crossmark","source":"Crossref","is-referenced-by-count":72,"title":["Enhanced mTORC1 signaling and protein synthesis in pathologic \u03b1-synuclein cellular and animal models of Parkinson\u2019s disease"],"prefix":"10.1126","volume":"15","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9744-9220","authenticated-orcid":true,"given":"Mohammed Repon","family":"Khan","sequence":"first","affiliation":[{"name":"Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, 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