論文

査読有り 国際誌
2019年5月

Runx2 is required for postnatal intervertebral disc tissue growth and development.

Journal of cellular physiology
  • Lifan Liao
  • ,
  • Hua Jiang
  • ,
  • Yunshan Fan
  • ,
  • Ronald S Lu
  • ,
  • Changli Wei
  • ,
  • Takeshi Takarada
  • ,
  • Shisheng He
  • ,
  • Di Chen

234
5
開始ページ
6679
終了ページ
6687
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1002/jcp.27410

Runx2 plays an essential role in embryonic disc tissue development in mice. However, the role of runt-related transcription factor 2 (Runx2) in postnatal disc tissue growth and development has not been defined. In the present studies, we generated Runx2 conditional knockout (KO) mice (Runx2Agc1ER ), in which Runx2 was deleted in Aggrecan-expressing cells in disc tissue at postnatal 2-weeks of age. We then analyzed changes in disc tissue growth and development using histology and immunohistochemical methods in 3-month-old mice. We found that large vacuolated notochordal cells were accumulated in the nucleus pulposus (NP) in Runx2 KO mice. The growth plate cartilage tissue in the disc was thicker in Runx2 KO mice. We also found a significant upregulation of Indian hedgehog (Ihh) expression in the cells in NP cells and in annulus fibrosus cells of Runx2 KO mice. These results demonstrated that Runx2 may play an important role in postnatal disc tissue development through interacting with Ihh signaling.

リンク情報
DOI
https://doi.org/10.1002/jcp.27410
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30341902
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460473
ID情報
  • DOI : 10.1002/jcp.27410
  • ISSN : 0021-9541
  • PubMed ID : 30341902
  • PubMed Central 記事ID : PMC6460473

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