mtDNA variability determines spontaneous joint aging damage in a conplastic mouse model.
8-Hydroxy-2'-Deoxyguanosine
Aging
/ physiology
Animals
Beclin-1
/ genetics
Caspase 3
/ metabolism
DNA, Mitochondrial
/ genetics
Disease Models, Animal
Ki-67 Antigen
/ metabolism
Matrix Metalloproteinase 13
/ metabolism
Mice
Mice, Inbred C57BL
Mitochondria
/ metabolism
Osteoarthritis
/ genetics
beta-Galactosidase
/ metabolism
autophagy
conplastic mice
mtDNA
oxidative stress
senescence
Journal
Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617
Informations de publication
Date de publication:
02 Jul 2022
02 Jul 2022
Historique:
received:
20
10
2021
accepted:
14
06
2022
pubmed:
3
7
2022
medline:
25
8
2022
entrez:
2
7
2022
Statut:
ppublish
Résumé
Mitochondria and mtDNA variations contribute to specific aspects of the aging process. Here, we aimed to investigate the influence of mtDNA variation on joint damage in a model of aging using conplastic mice. A conplastic (BL/6
Identifiants
pubmed: 35779570
pii: 204153
doi: 10.18632/aging.204153
pmc: PMC9417242
doi:
Substances chimiques
Beclin-1
0
DNA, Mitochondrial
0
Ki-67 Antigen
0
8-Hydroxy-2'-Deoxyguanosine
88847-89-6
beta-Galactosidase
EC 3.2.1.23
Caspase 3
EC 3.4.22.-
Matrix Metalloproteinase 13
EC 3.4.24.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
5966-5983Références
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