Overexpression of transcription factor FoxA2 in the developing skeleton causes an enlargement of the cartilage hypertrophic zone, but it does not trigger ectopic differentiation in immature chondrocytes.
Alkaline Phosphatase
/ metabolism
Animals
Bone and Bones
/ metabolism
Cartilage
/ metabolism
Cell Differentiation
/ genetics
Chondrocytes
/ metabolism
Core Binding Factor Alpha 1 Subunit
/ genetics
Hepatocyte Nuclear Factor 3-beta
/ genetics
Hypertrophy
Matrix Metalloproteinase 13
/ genetics
Mice
Transcription Factors
/ metabolism
Cartilage biology
Chondrocyte hypertrophy
Endochondral ossification
FoxA2
Runx2
Journal
Bone
ISSN: 1873-2763
Titre abrégé: Bone
Pays: United States
ID NLM: 8504048
Informations de publication
Date de publication:
07 2022
07 2022
Historique:
received:
21
12
2021
revised:
01
04
2022
accepted:
04
04
2022
pubmed:
11
4
2022
medline:
25
5
2022
entrez:
10
4
2022
Statut:
ppublish
Résumé
We previously found that FoxA factors are necessary for chondrocyte differentiation. To investigate whether FoxA factors alone are sufficient to drive chondrocyte hypertrophy, we build a FoxA2 transgenic mouse in which FoxA2 cDNA is driven by a reiterated Tetracycline Response Element (TRE) and a minimal CMV promoter. This transgenic line was crossed with a col2CRE;Rosa26
Identifiants
pubmed: 35398294
pii: S8756-3282(22)00094-1
doi: 10.1016/j.bone.2022.116418
pmc: PMC9133231
mid: NIHMS1808852
pii:
doi:
Substances chimiques
Core Binding Factor Alpha 1 Subunit
0
Foxa2 protein, mouse
0
Transcription Factors
0
Hepatocyte Nuclear Factor 3-beta
135845-92-0
Alkaline Phosphatase
EC 3.1.3.1
Matrix Metalloproteinase 13
EC 3.4.24.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
116418Subventions
Organisme : NIAMS NIH HHS
ID : R01 AR060735
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR069671
Pays : United States
Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.
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