Epiphyseal bone formation occurs via thyroid hormone regulation of chondrocyte to osteoblast transdifferentiation.
Epiphyseal bone formation occurs via thyroid hormone regulation of chondrocyte to osteoblast transdifferentiation.
复制标题
DOI:
10.1038/s41598-017-11050-1
复制
发表时间:
2017-09-05
影响因子:
4.6
通讯作者:
Mohan S
中科院分区:
文献类型:
--
作者:
Aghajanian P;Xing W;Cheng S;Mohan S
Endochondral ossification in the diaphysis of long bones has been studied in-depth during fetal development but not postnatally in the epiphysis. Immunohistochemical studies revealed that Sox9 and Col2 expressing immature chondrocytes in the epiphysis transition into prehypertrophic and hypetrophic chondrocytes and finally into osteoblasts expressing Col1 and BSP during postnatal day 7–10, when serum levels of thyroid hormone (TH) rise. Lineage tracing using Rosa-td tomato Col2-Cre-ERT2 mice treated with tamoxifen indicated that the same Col2 expressing chondrocytes expressed prehypertrophic, hypertrophic, and subsequently bone formation markers in a sequential manner in euthyroid but not hypothyroid mice, thus providing evidence that chondrocyte to osteoblast transdifferentiation is TH-dependent. Vascular invasion was apparent at the time of bone formation but not earlier. In vitro studies revealed that TH acting via TRα1 promoted expression of SHH while TRβ1 activation increased IHH but inhibited SHH expression. SHH promoted expression of markers of immature chondrocytes but inhibited chondrocyte hypertrophy while IHH promoted chondrocyte hypertrophy. Based on our data, we propose a model in which TH acting through TRα1 and TRβ1, respectively, fine tune levels of SHH and IHH and, thereby control the transit of proliferating immature chondrocytes into mature hypertrophic chondrocytes to become osteoblasts at the epiphysis.
登录
查看更多内容
影响因子:
4.8
作者:
Desouza LA;Sathanoori M;Kapoor R;Rajadhyaksha N;Gonzalez LE;Kottmann AH;Tole S;Vaidya VA
通讯作者:
Vaidya VA
影响因子:
4.6
作者:
Paul, Sandeep;Schindler, Simone;Crump, J. Gage
通讯作者:
Crump, J. Gage
影响因子:
7.2
作者:
Long, Fanxin;Ornitz, David M.
通讯作者:
Ornitz, David M.
DOI:
10.1038/mt.2013.222
发表时间:
2014-02
期刊:
Molecular therapy : the journal of the American Society of Gene Therapy
影响因子:
--
作者:
通讯作者:
--
影响因子:
11.4
作者:
Fraichard, A;Chassande, O;Samarut, J
通讯作者:
Samarut, J