Role of c-Myb in chondrogenesis
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25845979
DOI
10.1016/j.bone.2015.02.031
PII: S8756-3282(15)00107-6
Knihovny.cz E-resources
- Keywords
- Chondrogenesis, Endochondral bone, Micromass cultures, Mouse limbs, Up- and down-regulation, siRNA,
- MeSH
- Biomarkers metabolism MeSH
- Cell Differentiation MeSH
- Chondrogenesis physiology MeSH
- In Situ Hybridization MeSH
- Extremities embryology MeSH
- Mice MeSH
- Proto-Oncogene Proteins c-myb genetics physiology MeSH
- Gene Silencing MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- Proto-Oncogene Proteins c-myb MeSH
The Myb locus encodes the c-Myb transcription factor involved in controlling a broad variety of cellular processes. Recently, it has been shown that c-Myb may play a specific role in hard tissue formation; however, all of these results were gathered from an analysis of intramembranous ossification. To investigate a possible role of c-Myb in endochondral ossification, we carried out our study on the long bones of mouse limbs during embryonic development. Firstly, the c-myb expression pattern was analyzed by in situ hybridization during endochondral ossification of long bones. c-myb positive areas were found in proliferating as well as hypertrophic zones of the growth plate. At early embryonic stages, localized expression was also observed in the perichondrium and interdigital areas. The c-Myb protein was found in proliferating chondrocytes and in the perichondrium of the forelimb bones (E14.5-E17.5). Furthermore, protein was detected in pre-hypertrophic as well as hypertrophic chondrocytes. Gain-of-function and loss-of-function approaches were used to test the effect of altered c-myb expression on chondrogenesis in micromass cultures established from forelimb buds of mouse embryos. A loss-of-function approach using c-myb specific siRNA decreased nodule formation, as well as downregulated the level of Sox9 expression, a major marker of chondrogenesis. Transient c-myb overexpression markedly increased the formation of cartilage nodules and the production of extracellular matrix as detected by intense staining with Alcian blue. Moreover, the expression of early chondrogenic genes such as Sox9, Col2a1 and activity of a Col2-LUC reporter were increased in the cells overexpressing c-myb while late chondrogenic markers such as Col10a1 and Mmp13 were not significantly changed or were downregulated. Taken together, the results of this study demonstrate that the c-Myb transcription factor is involved in the regulation and promotion of endochondral bone formation.
Department of Craniofacial Development and Stem Cell Biology King's College London London UK
Department of Experimental Biology Faculty of Science Masaryk University Brno Czech Republic
Institute of Anatomy Charles University Prague Czech Republic
References provided by Crossref.org
Overexpression of c-Myb is associated with suppression of distant metastases in colorectal carcinoma
Caspases and osteogenic markers--in vitro screening of inhibition impact