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High mobility group AT-hook 2 regulates osteoblast differentiation and facial bone development.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2022 Jan 29; Vol. 590, pp. 68-74. Date of Electronic Publication: 2021 Dec 27. - Publication Year :
- 2022
-
Abstract
- The mutation and deletion of high mobility group AT-hook 2 (Hmga2) gene exhibit skeletal malformation, but almost nothing is known about the mechanism. This study examined morphological anomaly of facial bone in Hmga2 <superscript>-/-</superscript> mice and osteoblast differentiation of pre-osteoblast MC3T3-E1 cells with Hmga2 gene knockout (A2KO). Hmga2 <superscript>-/-</superscript> mice showed the size reduction of anterior frontal part of facial bones. Hmga2 protein and mRNA were expressed in mesenchymal cells at ossification area of nasal bone. A2KO cells differentiation into osteoblasts after reaching the proliferation plateau was strongly suppressed by alizarin red and alkaline phosphatase staining analyses. Expression of osteoblast-related genes, especially Osterix, was down-regulated in A2KO cells. These results demonstrate a close association of Hmga2 with osteoblast differentiation of mesenchymal cells and bone growth. Although future studies are needed, the present study suggests an involvement of Hmga2 in osteoblast-genesis and bone growth.<br />Competing Interests: Declaration of competing interest The authors declare that the research was conducted in the absence of any commercial of financial relationship that could be considered as a potential conflict of interest.<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Cell Line
Cell Proliferation
Cell Shape
Embryo, Mammalian metabolism
Gene Expression Regulation, Developmental
HMGA2 Protein genetics
Mice, Knockout
Mice
Bone Development
Cell Differentiation
Facial Bones growth & development
HMGA2 Protein metabolism
Osteoblasts cytology
Osteoblasts metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 590
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 34973532
- Full Text :
- https://doi.org/10.1016/j.bbrc.2021.12.093