SARM1 Ablation Is Protective and Preserves Spatial Vision in an In Vivo Mouse Model of Retinal Ganglion Cell Degeneration.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
30 Jan 2022
Historique:
received: 27 10 2021
revised: 21 01 2022
accepted: 26 01 2022
entrez: 15 2 2022
pubmed: 16 2 2022
medline: 15 3 2022
Statut: epublish

Résumé

The challenge of developing gene therapies for genetic forms of blindness is heightened by the heterogeneity of these conditions. However, mechanistic commonalities indicate key pathways that may be targeted in a gene-independent approach. Mitochondrial dysfunction and axon degeneration are common features of many neurodegenerative conditions including retinal degenerations. Here we explore the neuroprotective effect afforded by the absence of sterile alpha and Toll/interleukin-1 receptor motif-containing 1 (SARM1), a prodegenerative NADase, in a rotenone-induced mouse model of retinal ganglion cell loss and visual dysfunction.

Identifiants

pubmed: 35163535
pii: ijms23031606
doi: 10.3390/ijms23031606
pmc: PMC8835928
pii:
doi:

Substances chimiques

Armadillo Domain Proteins 0
Cytoskeletal Proteins 0
SARM1 protein, mouse 0
Rotenone 03L9OT429T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Science Foundation Ireland
ID : 16/IA/4452
Pays : Ireland
Organisme : Science Foundation Ireland
ID : 16/IA/4376
Pays : Ireland
Organisme : Irish Research Council
ID : GOIPG/2017/1631
Organisme : Health Research Board of Ireland
ID : HRAPOR-2015-1140
Organisme : Fighting Blindness Ireland - Health Research Board of Ireland - Health Research Charities Ireland
ID : MRCG-2012-4
Organisme : Fighting Blindness Ireland - Health Research Board of Ireland - Health Research Charities Ireland
ID : MRCG-2016-14

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Auteurs

Laura K Finnegan (LK)

Department of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.

Naomi Chadderton (N)

Department of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.

Paul F Kenna (PF)

Department of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.
The Research Foundation, Royal Victoria Eye and Ear Hospital, D02 XK51 Dublin, Ireland.

Arpad Palfi (A)

Department of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.

Michael Carty (M)

Trinity Biomedical Sciences Institute, The School of Biochemistry and Immunology, Trinity College Dublin, D02 R590 Dublin, Ireland.

Andrew G Bowie (AG)

Trinity Biomedical Sciences Institute, The School of Biochemistry and Immunology, Trinity College Dublin, D02 R590 Dublin, Ireland.

Sophia Millington-Ward (S)

Department of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.

G Jane Farrar (GJ)

Department of Genetics, The School of Genetics and Microbiology, Trinity College Dublin, D02 VF25 Dublin, Ireland.

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Classifications MeSH