PINK1-mediated Drp1
Journal
Signal transduction and targeted therapy
ISSN: 2059-3635
Titre abrégé: Signal Transduct Target Ther
Pays: England
ID NLM: 101676423
Informations de publication
Date de publication:
15 04 2022
15 04 2022
Historique:
received:
21
09
2021
accepted:
14
02
2022
revised:
09
02
2022
entrez:
15
4
2022
pubmed:
16
4
2022
medline:
19
4
2022
Statut:
epublish
Résumé
Dynamic change of mitochondrial morphology and distribution along neuronal branches are essential for neural circuitry formation and synaptic efficacy. However, the underlying mechanism remains elusive. We show here that Pink1 knockout (KO) mice display defective dendritic spine maturation, reduced axonal synaptic vesicles, abnormal synaptic connection, and attenuated long-term synaptic potentiation (LTP). Drp1 activation via S616 phosphorylation rescues deficits of spine maturation in Pink1 KO neurons. Notably, mice harboring a knockin (KI) phosphor-null Drp1
Identifiants
pubmed: 35422062
doi: 10.1038/s41392-022-00933-z
pii: 10.1038/s41392-022-00933-z
pmc: PMC9010405
doi:
Substances chimiques
Protein Kinases
EC 2.7.-
PTEN-induced putative kinase
EC 2.7.11.1
Dynamins
EC 3.6.5.5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
103Subventions
Organisme : NIDDK NIH HHS
ID : R01 DK002001
Pays : United States
Organisme : NIDDK NIH HHS
ID : R56 DK002001
Pays : United States
Informations de copyright
© 2022. The Author(s).
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