Details

Autor(en) / Beteiligte

• Yan, Xue
• Fan, Deng‐Yun
• Pi, Ya‐Lei
• Zhang, Ya‐Nan
• Fu, Peng‐Jiu
• Zhang, Hui‐Feng

Titel

ERα/β/DMP1 axis promotes trans‐differentiation of chondrocytes to bone cells through GSK‐3β/β‐catenin pathway

Ist Teil von

• Journal of anatomy, 2022-06, Vol.240 (6), p.1152-1161

Ort / Verlag

England: Wiley Subscription Services, Inc

Erscheinungsjahr

2022

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• Estrogen‐induced premature closing of the growth plate in the long bones is a major cause of short stature after premature puberty. Recent studies have found that chondrocytes can directly trans‐differentiate into osteoblasts in the process of endochondral bone formation, which indicates that cartilage formation and osteogenesis may be a continuous biological process. However, whether estrogen promotes the direct trans‐differentiation of chondrocytes into osteoblasts remains largely unknown. Chondrocytes were treated with different concentrations of 17β‐estradiol, and Alizarin Red staining and alkaline phosphatase activity assay were used to detected osteogenesis. Specific short hairpin RNA and tamoxifen were used to block the estrogen receptor (ER) pathway and osteogenic marker genes and downstream gene expression were detected using real‐time quantitative polymerase chain reaction, western blot, and immunohistochemistry staining. The findings showed that 17β‐estradiol promoted the chondrocyte osteogenesis in vitro, even at high concentrations. In addition, blocking of the ERα/β pathway inhibited the trans‐differentiation of chondrocytes into osteogenic cells. Furthermore, we found that dentin matrix protein 1 (DMP1), which is a direct downstream molecular of ER, was involved in 17β‐estradiol/ER pathway‐regulated osteogenesis. As well, glycogen synthase kinase‐3 beta (GSK‐3β)/β‐catenin signal pathway also participates in ERα/β/DMP1‐regulated chondrocyte osteogenesis. The GSK‐3β/β‐catenin signal pathway was involved in ERα/β/DMP1‐regulated chondrocyte osteogenesis. These findings suggest that ER/DMP1/GSK‐3β/β‐catenin plays a vital role in estrogen regulation of chondrocyte osteogenesis and provide a therapeutic target for short stature caused by epiphyseal fusion. Here, we demonstrate that 17β‐estradiol promotes the chondrocyte osteogenesis in vitro and obstruction of the estrogen receptor (ER)α/β pathway inhibits the trans‐differentiation of chondrocytes into osteogenic cells. Dentin matrix protein 1 (DMP1), which is a direct downstream molecular of ER, was involved in 17β‐estradiol/ER pathway‐regulated osteogenesis. The glycogen synthase kinase‐3 beta (GSK‐3β)/β‐catenin signal pathway also participates in osteogenesis regulated by ERα/β/DMP1 chondrocytes.