FOXO1 expression in chondrocytes modulates cartilage production and removal in fracture healing.
Cartilage
Chondrocyte
Fracture
Healing
Inflammation
Osteoclast
Journal
Bone
ISSN: 1873-2763
Titre abrégé: Bone
Pays: United States
ID NLM: 8504048
Informations de publication
Date de publication:
07 2021
07 2021
Historique:
received:
26
02
2020
revised:
15
02
2021
accepted:
24
02
2021
pubmed:
5
3
2021
medline:
10
7
2021
entrez:
4
3
2021
Statut:
ppublish
Résumé
Fracture healing is a multistage process characterized by inflammation, cartilage formation, bone deposition, and remodeling. Chondrocytes are important in producing cartilage that forms the initial anlagen for the hard callus needed to stabilize the fracture site. We examined the role of FOXO1 by selective ablation of FOXO1 in chondrocytes mediated by Col2α1 driven Cre recombinase. Experimental mice with lineage-specific FOXO1 deletion (Col2α1Cre
Identifiants
pubmed: 33662610
pii: S8756-3282(21)00067-3
doi: 10.1016/j.bone.2021.115905
pmc: PMC8106874
mid: NIHMS1685192
pii:
doi:
Substances chimiques
Forkhead Box Protein O1
0
Foxo1 protein, mouse
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
115905Subventions
Organisme : NIAMS NIH HHS
ID : R01 AR060055
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE017732
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE027074
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR069619
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE019108
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Inc. All rights reserved.
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