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Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis

Ubiquitin C-terminal hydrolase L1 (UCH-L1) is a deubiquitinating enzyme that is highly expressed in neurons, and gathering evidence indicates that UCH-L1 may play pathogenic roles in many neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease (PD). Additionally, li...

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Autores principales: Kang, Seo-Jun, Kim, Jin Soo, Park, Sang Myun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221840/
https://www.ncbi.nlm.nih.gov/pubmed/30429647
http://dx.doi.org/10.5607/en.2018.27.5.377
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author Kang, Seo-Jun
Kim, Jin Soo
Park, Sang Myun
author_facet Kang, Seo-Jun
Kim, Jin Soo
Park, Sang Myun
author_sort Kang, Seo-Jun
collection PubMed
description Ubiquitin C-terminal hydrolase L1 (UCH-L1) is a deubiquitinating enzyme that is highly expressed in neurons, and gathering evidence indicates that UCH-L1 may play pathogenic roles in many neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease (PD). Additionally, lipid rafts have attracted interest in neurodegeneration as playing a common role in many neurodegenerative diseases. In the present study, we demonstrated that UCH-L1 associates with lipid rafts as with other PD-associated gene products. In addition, UCH-L1 regulates lipid raft-dependent endocytosis and it is not dependent on the expression and degradation of caveolin-1 or flotillin-1. Finally, UCH-L1 regulates cell-to-cell transmission of α-synuclein. This study provides evidence that many PD-associated gene products share common signaling pathways to explain the pathogenesis of PD.
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spelling pubmed-62218402018-11-14 Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis Kang, Seo-Jun Kim, Jin Soo Park, Sang Myun Exp Neurobiol Original Article Ubiquitin C-terminal hydrolase L1 (UCH-L1) is a deubiquitinating enzyme that is highly expressed in neurons, and gathering evidence indicates that UCH-L1 may play pathogenic roles in many neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease (PD). Additionally, lipid rafts have attracted interest in neurodegeneration as playing a common role in many neurodegenerative diseases. In the present study, we demonstrated that UCH-L1 associates with lipid rafts as with other PD-associated gene products. In addition, UCH-L1 regulates lipid raft-dependent endocytosis and it is not dependent on the expression and degradation of caveolin-1 or flotillin-1. Finally, UCH-L1 regulates cell-to-cell transmission of α-synuclein. This study provides evidence that many PD-associated gene products share common signaling pathways to explain the pathogenesis of PD. The Korean Society for Brain and Neural Science 2018-10 2018-10-31 /pmc/articles/PMC6221840/ /pubmed/30429647 http://dx.doi.org/10.5607/en.2018.27.5.377 Text en Copyright © Experimental Neurobiology 2018. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kang, Seo-Jun
Kim, Jin Soo
Park, Sang Myun
Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis
title Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis
title_full Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis
title_fullStr Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis
title_full_unstemmed Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis
title_short Ubiquitin C-terminal Hydrolase L1 Regulates Lipid Raft-dependent Endocytosis
title_sort ubiquitin c-terminal hydrolase l1 regulates lipid raft-dependent endocytosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221840/
https://www.ncbi.nlm.nih.gov/pubmed/30429647
http://dx.doi.org/10.5607/en.2018.27.5.377
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