Multi-omic approach characterises the neuroprotective role of retromer in regulating lysosomal health.
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Peer-reviewed
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Abstract
Retromer controls cellular homeostasis through regulating integral membrane protein sorting and transport and by controlling maturation of the endo-lysosomal network. Retromer dysfunction, which is linked to neurodegenerative disorders including Parkinson's and Alzheimer's diseases, manifests in complex cellular phenotypes, though the precise nature of this dysfunction, and its relation to neurodegeneration, remain unclear. Here, we perform an integrated multi-omics approach to provide precise insight into the impact of Retromer dysfunction on endo-lysosomal health and homeostasis within a human neuroglioma cell model. We quantify widespread changes to the lysosomal proteome, indicative of broad lysosomal dysfunction and inefficient autophagic lysosome reformation, coupled with a reconfigured cell surface proteome and secretome reflective of increased lysosomal exocytosis. Through this global proteomic approach and parallel transcriptomic analysis, we provide a holistic view of Retromer function in regulating lysosomal homeostasis and emphasise its role in neuroprotection.
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Acknowledgements: The authors thank the Wolfson Bioimaging Facility and Bristol Proteomics Facility for their support. px458 plasmids targeting exons 2 and 3 of VPS29 were cloned by Dr Kerrie McNally. P.J.C. was supported by the Wellcome Trust (104568/Z/14/Z and 220260/Z/20/Z), the Medical Research Council (MRC) (MR/L007363/1 and MR/P018807/1), the Lister Institute of Preventive Medicine, and the award of a Royal Society Noreen Murray Research Professorship (RSRP/R1/211004). J.L.D. was supported by a Wellcome Trust Dynamic Molecular Cell Biology PhD Studentship (203959/Z/16/Z) and a Wellcome Early Career Award (225128/Z/22/Z). J.R.E. is supported by a Sir Henry Dale Fellowship jointly funded by the Wellcome Trust and the Royal Society (216370/Z/19/Z). This work was supported by Italian Telethon Foundation (TIGEM institutional grant), European Research Council H2020 AdG (LYSOSOMICS 694282 to A.B.), Associazione Italiana per la Ricerca sul Cancro A.I.R.C. (IG-22103 to A.B.) and National Institute of Aging, NIH, USA (AG045781 to W.C.X.).
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2041-1723

