Regulation of Skeletal Development and Maintenance by Runx2 and Sp7.
Cbfb
Runx2
Sp7
bone matrix protein genes
chondrocyte differentiation
osteoarthritis
osteoblast differentiation
osteoblast proliferation
osteocalcin
osteocyte processes
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
20 Sep 2024
20 Sep 2024
Historique:
received:
29
07
2024
revised:
16
09
2024
accepted:
18
09
2024
medline:
29
9
2024
pubmed:
28
9
2024
entrez:
28
9
2024
Statut:
epublish
Résumé
Runx2 (runt related transcription factor 2) and Sp7 (Sp7 transcription factor 7) are crucial transcription factors for bone development. The cotranscription factor Cbfb (core binding factor beta), which enhances the DNA-binding capacity of Runx2 and stabilizes the Runx2 protein, is necessary for bone development. Runx2 is essential for chondrocyte maturation, and Sp7 is partly involved. Runx2 induces the commitment of multipotent mesenchymal cells to osteoblast lineage cells and enhances the proliferation of osteoprogenitors. Reciprocal regulation between Runx2 and the Hedgehog, fibroblast growth factor (Fgf), Wnt, and parathyroid hormone-like hormone (Pthlh) signaling pathways and Dlx5 (distal-less homeobox 5) plays an important role in these processes. The induction of Fgfr2 (Fgf receptor 2) and Fgfr3 expression by Runx2 is important for the proliferation of osteoblast lineage cells. Runx2 induces Sp7 expression, and Runx2
Identifiants
pubmed: 39337587
pii: ijms251810102
doi: 10.3390/ijms251810102
pii:
doi:
Substances chimiques
Core Binding Factor Alpha 1 Subunit
0
Sp7 Transcription Factor
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : the Japanese Ministry of Education, Culture, Sports, Science and Technology
ID : 23H00440