FNDC-1-mediated mitophagy and ATFS-1 coordinate to protect against hypoxia-reoxygenation.
Animals
Animals, Genetically Modified
Caenorhabditis elegans
/ genetics
Caenorhabditis elegans Proteins
/ genetics
Genes, Helminth
Hypoxia
/ genetics
Loss of Function Mutation
Membrane Proteins
/ genetics
Mitochondrial Proteins
/ genetics
Mitophagy
/ genetics
Reperfusion Injury
/ genetics
Transcription Factors
/ genetics
C. elegans
hypoxia-reoxygenation (HR)
metabolism
mitochondrial unfolded protein response (UPRmt)
mitophagy
Journal
Autophagy
ISSN: 1554-8635
Titre abrégé: Autophagy
Pays: United States
ID NLM: 101265188
Informations de publication
Date de publication:
11 2021
11 2021
Historique:
pubmed:
9
1
2021
medline:
25
3
2022
entrez:
8
1
2021
Statut:
ppublish
Résumé
Mitochondrial quality control (MQC) balances organelle adaptation and elimination, and mechanistic crosstalk between the underlying molecular processes affects subsequent stress outcomes. FUNDC1 (FUN14 domain containing 1) is a mammalian mitophagy receptor that responds to hypoxia-reoxygenation (HR) stress. Here, we provide evidence that FNDC-1 is the
Identifiants
pubmed: 33416042
doi: 10.1080/15548627.2021.1872885
pmc: PMC8632273
doi:
Substances chimiques
ATFS-1 protein, C elegans
0
Caenorhabditis elegans Proteins
0
Membrane Proteins
0
Mitochondrial Proteins
0
Transcription Factors
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
3389-3401Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL071158
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS092558
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM101972
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL127891
Pays : United States
Organisme : NINDS NIH HHS
ID : R21 NS102780
Pays : United States
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