AAV-Mediated GALC Gene Therapy Rescues Alpha-Synucleinopathy in the Spinal Cord of a Leukodystrophic Lysosomal Storage Disease Mouse Model.
Parkinson's disease
alpha-synuclein
globoid cell leukodystrophy
proteinopathies
spinal cord
Journal
Frontiers in cellular neuroscience
ISSN: 1662-5102
Titre abrégé: Front Cell Neurosci
Pays: Switzerland
ID NLM: 101477935
Informations de publication
Date de publication:
2020
2020
Historique:
received:
20
10
2020
accepted:
30
11
2020
entrez:
11
1
2021
pubmed:
12
1
2021
medline:
12
1
2021
Statut:
epublish
Résumé
Krabbe's disease (KD) is primarily a demyelinating disorder, but recent studies have identified the presence of neuronal protein aggregates in the brain, at least partially composed by alpha-synuclein (α-syn). The role of this protein aggregation in the pathogenesis of KD is largely unknown, but it has added KD to a growing list of lysosomal storage diseases that can be also be considered as proteinopathies. While the presence of these protein aggregates within the KD brain is now appreciated, the remainder of the central nervous system (CNS) remains uncharacterized. This study is the first to report the presence of thioflavin-S reactive inclusions throughout the spinal cord of both murine and human spinal tissue. Stereological analysis revealed the temporal and spatial accumulation of these inclusions within the neurons of the ventral spinal cord vs. those located in the dorsal cord. This study also confirmed that these thio-S positive accumulations are present within neuronal populations and are made up at least in part by α-syn in both the twitcher mouse and cord autopsied material from affected human patients. Significantly, neonatal gene therapy for galactosylceramidase, a treatment that strongly improves the survival and health of KD mice, but not bone marrow transplantation prevents the formation of these inclusions in spinal neurons. These results expand the understanding of α-syn protein aggregation within the CNS of individuals afflicted with KD and underlines the tractability of this problem via early gene therapy, with potential impact to other synucleinopathies such as PD.
Identifiants
pubmed: 33424556
doi: 10.3389/fncel.2020.619712
pmc: PMC7785790
doi:
Types de publication
Journal Article
Langues
eng
Pagination
619712Informations de copyright
Copyright © 2020 Marshall, Issa, Heller, Nguyen and Bongarzone.
Déclaration de conflit d'intérêts
EB is a consultant for Lysosomal Therapeutics Inc., E-Scape Bio, Gain Therapeutics, Affinia, and Neurogene. Neither entity provided support in the form of salaries for any listed author nor played additional roles in the study design, data collection, analysis, decision to publish, or preparation of the manuscript. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Mol Genet Metab. 2012 Sep;107(1-2):186-96
pubmed: 22704480
Acta Neuropathol. 1984;62(4):298-308
pubmed: 6730907
Front Aging Neurosci. 2018 Dec 13;10:402
pubmed: 30618709
J Neuropathol Exp Neurol. 1971 Jan;30(1):145
pubmed: 5542535
Brain. 2013 Sep;136(Pt 9):2649-51
pubmed: 24137751
J Pathol. 2014 Apr;232(5):509-21
pubmed: 24415155
Neurology. 2019 Aug 13;93(7):302-309
pubmed: 31405935
Acta Neuropathol. 2012 Nov;124(5):643-64
pubmed: 22926675
Mov Disord. 2011 Aug 1;26(9):1593-604
pubmed: 21618611
Mol Genet Metab. 2011 Apr;102(4):436-47
pubmed: 21257328
J Biol Chem. 2011 Aug 12;286(32):28080-8
pubmed: 21653695
Front Oncol. 2019 Apr 24;9:297
pubmed: 31069169
Acta Neuropathol. 2016 Apr;131(4):539-48
pubmed: 26820848
Cell. 2011 Jul 8;146(1):37-52
pubmed: 21700325
N Engl J Med. 2009 Oct 22;361(17):1651-61
pubmed: 19846850
Brain. 2014 May;137(Pt 5):1304-22
pubmed: 24531622
J Neurosci Res. 2016 Dec;94(12):1520-1530
pubmed: 27426866
J Clin Invest. 2020 Sep 1;130(9):4906-4920
pubmed: 32773406
Nature. 1997 Aug 28;388(6645):839-40
pubmed: 9278044
J Inherit Metab Dis. 2010 Apr;33(2):167-73
pubmed: 20177787
Behav Brain Res. 1987 Aug;25(2):143-53
pubmed: 3675825
J Neurosci. 2013 Jun 12;33(24):10048-56
pubmed: 23761900
J Lipid Res. 1980 Jan;21(1):53-64
pubmed: 7354254
Neuropathology. 2007 Oct;27(5):484-93
pubmed: 18018485
Mol Ther. 2018 Mar 7;26(3):874-889
pubmed: 29433937
J Neurosci Res. 2016 Nov;94(11):1328-32
pubmed: 27638614
J Neuropathol Exp Neurol. 1977 Jan;36(1):84-99
pubmed: 833619
Pediatrics. 2006 Sep;118(3):e879-89
pubmed: 16923928
Neurotoxicology. 2009 Nov;30(6):1127-32
pubmed: 19576930
J Neurol Neurosurg Psychiatry. 2008 Apr;79(4):368-76
pubmed: 18344392
Neuropathology. 2008 Feb;28(1):74-80
pubmed: 18031467
ASN Neuro. 2011;3(4):
pubmed: 21929508
J Inherit Metab Dis. 2013 May;36(3):575-80
pubmed: 22968580
Orphanet J Rare Dis. 2019 Feb 18;14(1):46
pubmed: 30777126
J Neurosci. 1992 Dec;12(12):4890-7
pubmed: 1281497
Acta Neuropathol. 2011 Jul;122(1):35-48
pubmed: 21373782
Neurobiol Dis. 2012 May;46(2):325-35
pubmed: 22326830
Ann Neurol. 2012 Oct;72(4):517-24
pubmed: 23109146
Am J Med Genet A. 2012 Nov;158A(11):2835-42
pubmed: 22991292
Biol Blood Marrow Transplant. 2018 Nov;24(11):2233-2238
pubmed: 29933067
Ann Neurol. 2015 Jul;78(1):142-9
pubmed: 25893830
Lancet Neurol. 2006 Mar;5(3):235-45
pubmed: 16488379
Nat Genet. 2017 Oct;49(10):1511-1516
pubmed: 28892059
Sci Rep. 2018 Aug 20;8(1):12462
pubmed: 30127535
PLoS One. 2017 Sep 14;12(9):e0184731
pubmed: 28910367
Acta Neuropathol. 2007 Apr;113(4):421-9
pubmed: 17294202
J Neurosci. 2011 Jul 6;31(27):9945-57
pubmed: 21734286
J Neurochem. 1996 Mar;66(3):1118-24
pubmed: 8769874
J Neurosci Res. 2016 Nov;94(11):1138-51
pubmed: 27638599
Neuron. 2017 Feb 22;93(4):737-746
pubmed: 28231462
J Spinal Cord Med. 2020 Nov;43(6):832-845
pubmed: 30620687
Science. 1984 May 18;224(4650):753-5
pubmed: 6719111
PLoS One. 2018 Feb 26;13(2):e0193438
pubmed: 29481565