{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,2]],"date-time":"2026-10-02T13:11:30Z","timestamp":1790946690522,"version":"4.1.0"},"reference-count":59,"publisher":"MDPI AG","issue":"15","license":[{"start":{"date-parts":[[2022,7,29]],"date-time":"2022-07-29T00:00:00Z","timestamp":1659052800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Ministero dell\u2019Universit\u00e0 e della Ricerca","award":["PRIN 2017"],"award-info":[{"award-number":["PRIN 2017"]}]},{"name":"Ministero dell\u2019Universit\u00e0 e della Ricerca","award":["cariplo2015"],"award-info":[{"award-number":["cariplo2015"]}]},{"name":"Cariplo foundation","award":["PRIN 2017"],"award-info":[{"award-number":["PRIN 2017"]}]},{"name":"Cariplo foundation","award":["cariplo2015"],"award-info":[{"award-number":["cariplo2015"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cells"],"abstract":"<jats:p>\u03b2-glucocerebrosidase is a lysosomal hydrolase involved in the catabolism of the sphingolipid glucosylceramide. Biallelic loss of function mutations in this enzyme are responsible for the onset of Gaucher disease, while monoallelic \u03b2-glucocerebrosidase mutations represent the first genetic risk factor for Parkinson\u2019s disease. Despite this evidence, the molecular mechanism linking the impairment in \u03b2-glucocerebrosidase activity with the onset of neurodegeneration in still unknown. In this frame, we developed two in vitro neuronal models of \u03b2-glucocerebrosidase deficiency, represented by mouse cerebellar granule neurons and human-induced pluripotent stem cells-derived dopaminergic neurons treated with the specific \u03b2-glucocerebrosidase inhibitor conduritol B epoxide. Neurons deficient for \u03b2-glucocerebrosidase activity showed a lysosomal accumulation of glucosylceramide and the onset of neuronal damage. Moreover, we found that neurons react to the lysosomal impairment by the induction of their biogenesis and exocytosis. This latter event was responsible for glucosylceramide accumulation also at the plasma membrane level, with an alteration in lipid and protein composition of specific signaling microdomains. Collectively, our data suggest that \u03b2-glucocerebrosidase loss of function impairs the lysosomal compartment, establishing a lysosome\u2013plasma membrane axis responsible for modifications in the plasma membrane architecture and possible alterations of intracellular signaling pathways, leading to neuronal damage.<\/jats:p>","DOI":"10.3390\/cells11152343","type":"journal-article","created":{"date-parts":[[2022,7,31]],"date-time":"2022-07-31T21:49:02Z","timestamp":1659304142000},"page":"2343","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":22,"title":["\u03b2-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration"],"prefix":"10.3390","volume":"11","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3099-3395","authenticated-orcid":false,"given":"Giulia","family":"Lunghi","sequence":"first","affiliation":[{"name":"Department of Medical 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Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0972-610X","authenticated-orcid":false,"given":"Giulia","family":"Sold\u00e0","sequence":"additional","affiliation":[{"name":"Department of Biomedical Sciences, Humanitas University, 20090 Milan, Italy"},{"name":"Humanitas Clinical and Research Center\u2014IRCCS, Via Manzoni 56, 20072 Milan, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6478-026X","authenticated-orcid":false,"given":"Alessio","family":"Di Fonzo","sequence":"additional","affiliation":[{"name":"IRCCS Foundation Ca\u2019 Granda Ospedale Maggiore Policlinico, Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5375-2404","authenticated-orcid":false,"given":"Emanuele","family":"Frattini","sequence":"additional","affiliation":[{"name":"IRCCS Foundation Ca\u2019 Granda Ospedale Maggiore Policlinico, Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Manuela","family":"Magni","sequence":"additional","affiliation":[{"name":"IRCCS Foundation Ca\u2019 Granda Ospedale Maggiore Policlinico, Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, 20122 Milan, Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2112-4753","authenticated-orcid":false,"given":"Nara","family":"Liessi","sequence":"additional","affiliation":[{"name":"Analytical Chemistry 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