17
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Loss of Sox9 function results in defective chondrocyte differentiation of mouse embryonic stem cells in vitro.

      The International journal of developmental biology

      Amino Acid Sequence, Animals, Base Sequence, Cartilage, cytology, growth & development, Cell Differentiation, genetics, physiology, Chondrocytes, chemistry, metabolism, Chondrogenesis, Clone Cells, Collagen Type II, DNA, Embryonic Stem Cells, Exons, Gene Expression Regulation, Developmental, Gene Targeting, High Mobility Group Proteins, deficiency, Mice, Molecular Sequence Data, Reverse Transcriptase Polymerase Chain Reaction, SOX9 Transcription Factor, Transcription Factors

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The transcription factor Sox9 plays an important role during chondrogenesis. After early conditional inactivation of Sox9 in mesenchymal limb bud cells of mice, mesenchymal condensations as well as cartilage and bone are completely absent in the developing limbs. We analyzed chondrogenic differentiation of Sox9-/- mouse embryonic stem cells in vitro, using two clones with different targeted mutations. We found that the development of mature and hypertrophic chondrocytes is completely inhibited in the absence of Sox9 confirming that Sox9 is required for the formation of cartilage. In contrast, Sox9+/- mouse embryonic stem cells showed continuous but reduced differentiation into mature chondrocytes. Interestingly, the formation of early chondrogenic condensations expressing characteristic marker genes such as scleraxis, Sox5 and Sox6 was not inhibited in the absence of Sox9 in vitro. Thus, we propose that the earliest step of chondrogenesis could be regulated by a non cell-autonomous function of Sox9.

          Related collections

          Author and article information

          Journal
          18415932
          10.1387/ijdb.072490gh

          Comments

          Comment on this article