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68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment
Leucine-rich repeat kinase 2 is a large protein with implications in genetic and sporadic causes of Parkinson's disease. The physiological functions of LRRK2 are largely unknown. In this report, we investigated whether LRRK2 alters neural transport using live-cell imaging techniques and human n...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222795/ https://www.ncbi.nlm.nih.gov/pubmed/28119604 http://dx.doi.org/10.3389/fnagi.2016.00337 |
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author | Thomas, Joseph M. Li, Tianxia Yang, Wei Xue, Fengtian Fishman, Paul S. Smith, Wanli W. |
author_facet | Thomas, Joseph M. Li, Tianxia Yang, Wei Xue, Fengtian Fishman, Paul S. Smith, Wanli W. |
author_sort | Thomas, Joseph M. |
collection | PubMed |
description | Leucine-rich repeat kinase 2 is a large protein with implications in genetic and sporadic causes of Parkinson's disease. The physiological functions of LRRK2 are largely unknown. In this report, we investigated whether LRRK2 alters neural transport using live-cell imaging techniques and human neuroblastoma SH-SY5Y cells. Our results demonstrated that expression of the PD-linked mutant, LRRK2-R1441C, induced mitochondrial, and lysosomal transport defects in neurites of SH-SY5Y cells. Most importantly, recently identified GTP-binding inhibitors, 68 and FX2149, can reduce LRRK2 GTP-binding activity and attenuates R1441C-induced mitochondrial and lysosomal transport impairments. These results provide direct evidence and an early mechanism for neurite injury underlying LRRK2-induced neurodegeneration. This is the first report to show that LRRK2 GTP-binding activity plays a critical role during neurite transport, suggesting inhibition of LRRK2 GTP-binding could be a potential novel strategy for PD intervention. |
format | Online Article Text |
id | pubmed-5222795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52227952017-01-24 68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment Thomas, Joseph M. Li, Tianxia Yang, Wei Xue, Fengtian Fishman, Paul S. Smith, Wanli W. Front Aging Neurosci Neuroscience Leucine-rich repeat kinase 2 is a large protein with implications in genetic and sporadic causes of Parkinson's disease. The physiological functions of LRRK2 are largely unknown. In this report, we investigated whether LRRK2 alters neural transport using live-cell imaging techniques and human neuroblastoma SH-SY5Y cells. Our results demonstrated that expression of the PD-linked mutant, LRRK2-R1441C, induced mitochondrial, and lysosomal transport defects in neurites of SH-SY5Y cells. Most importantly, recently identified GTP-binding inhibitors, 68 and FX2149, can reduce LRRK2 GTP-binding activity and attenuates R1441C-induced mitochondrial and lysosomal transport impairments. These results provide direct evidence and an early mechanism for neurite injury underlying LRRK2-induced neurodegeneration. This is the first report to show that LRRK2 GTP-binding activity plays a critical role during neurite transport, suggesting inhibition of LRRK2 GTP-binding could be a potential novel strategy for PD intervention. Frontiers Media S.A. 2017-01-10 /pmc/articles/PMC5222795/ /pubmed/28119604 http://dx.doi.org/10.3389/fnagi.2016.00337 Text en Copyright © 2017 Thomas, Li, Yang, Xue, Fishman and Smith. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Thomas, Joseph M. Li, Tianxia Yang, Wei Xue, Fengtian Fishman, Paul S. Smith, Wanli W. 68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment |
title | 68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment |
title_full | 68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment |
title_fullStr | 68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment |
title_full_unstemmed | 68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment |
title_short | 68 and FX2149 Attenuate Mutant LRRK2-R1441C-Induced Neural Transport Impairment |
title_sort | 68 and fx2149 attenuate mutant lrrk2-r1441c-induced neural transport impairment |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5222795/ https://www.ncbi.nlm.nih.gov/pubmed/28119604 http://dx.doi.org/10.3389/fnagi.2016.00337 |
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