An immunohistochemistry study of sox9, runx2, and osterix expression in the mandibular cartilages of newborn mouse.

The purpose of this study is to investigate the spacial expression pattern and functional significance of three key transcription factors related to bone and cartilage formation, namely, Sox9, Runx2, and Osterix in cartilages during the late development of mouse mandible. Immunohistochemical examina...

Descripción completa

Detalles Bibliográficos
Publicado en:BioMed Research International Vol. 2013; pp. 265380 - 265381
Autores principales: Zhang, Hong, Zhao, Xiaopeng, Zhang, Zhiguang, Chen, Weiwei, Zhang, Xinli
Formato: research Journal Article
Publicado: Wiley-Blackwell 2013
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=109857916&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 109857916
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        23146133
        FT2T
      jtl: BioMed Research International
      issn: 23146133
      maglogo: N
    pubinfo:
      dt: 2013
      vid: 2013
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
    artinfo:
      ui:
        109857916
        2012152563
        10.1155/2013/265380
        NLM23762831
        PMC3671271
        109857916
      ppf: 265380
      ppct: 1
      formats:
        fmt:
          @attributes:
            type: P
      tig:
        atl: An immunohistochemistry study of sox9, runx2, and osterix expression in the mandibular cartilages of newborn mouse.
      aug:
        au:
          Zhang, Hong
          Zhao, Xiaopeng
          Zhang, Zhiguang
          Chen, Weiwei
          Zhang, Xinli
        affil: Department of Orthodontics, Guanghua School of Stomatology, Sun Yat-Sen University, Guangzhou 510055, China ; Dental and Craniofacial Research Institute, School of Dentistry, University of California, Los Angeles, CA, 90095, USA.
      sug:
        subj:
          Cartilage Metabolism
          Mandible Metabolism
          Proteins Metabolism
          Transcription Factors Metabolism
          Animal Population Groups
          Animal Studies
          Cartilage
          Chondrocytes
          Chondrocytes Metabolism
          Immunohistochemistry
          Mandible
          Mice
          Models, Biological
          Osteoblasts
          Osteoblasts Metabolism
      ab: The purpose of this study is to investigate the spacial expression pattern and functional significance of three key transcription factors related to bone and cartilage formation, namely, Sox9, Runx2, and Osterix in cartilages during the late development of mouse mandible. Immunohistochemical examinations of Sox9, Runx2, and Osterix were conducted in the mandibular cartilages of the 15 neonatal C57BL/6N mice. In secondary cartilages, both Sox9 and Runx2 were weakly expressed in the polymorphic cell zone, strongly expressed in the flattened cell zone and throughout the entire hypertrophic cell zone. Similarly, both transcriptional factors were weakly expressed in the uncalcified Meckel's cartilage while strongly expressed in the rostral cartilage. Meanwhile, Osterix was at an extremely low level in cells of the flattened cell zone and the upper hypertrophic cell zone in secondary cartilages. Surprisingly, Osterix was intensely expressed in hypertrophic chondrocytes in the center of the uncalcified Meckel's cartilage while moderately expressed in part of hypertrophic chondrocytes in the rostral process. Consequently, it is suggested that Sox9 is a main and unique positive regulator in the hypertrophic differentiation process of mandibular secondary cartilages, in addition to Runx2. Furthermore, Osterix is likely responsible for phenotypic conversion of Meckel's chondrocytes during its degeneration.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N