1,25(OH)2D3 inhibits osteogenic differentiation through activating β‑catenin signaling via downregulating bone morphogenetic protein 2.

The present study explored whether bone morphogenetic proteins (BMPs) and Wnt/beta-catenin signaling pathways were involved in the 1,25(OH)(2)D-3-induced inhibition of osteogenic differentiation in bone marrow-derived mesenchymal stem cells (BMSCs). To evaluate the osteogenic differentiation of BMSCs, the expression levels of ossification markers, including BMP2, Runt-related transcription factor 2 (Runx2), Msh homeobox 2 (Msx2), osteopontin (OPN) and osteocalcin (OCN), and the activity of alkaline phosphatase (ALP), as well as the calcified area observed by Alizarin red-S staining, were investigated. Chromatin immunoprecipitation (ChIP) assay was used to detect the effect of 1,25(OH)(2)D-3 on the DNA methylation and histone modification of BMP2, while an immunoprecipitation (IP) assay was performed to assess the crosstalk between Smad1 and disheveled-1 (Dvl-1) proteins. It was observed that 1,25(OH)(2)D-3 significantly decreased the expression levels of BMP2, Runx2, Msx2, OPN and OCN, and reduced ALP activity and the calcified area in BMSCs, whereas these effects were rescued by BMP2 overexpression. ChIP assay revealed that BMSCs treated with 1,25(OH)(2)D-3 exhibited a significant increase in H3K9me2 level and a decrease in the acetylation of histone H3 at the same BMP2 promoter region. In addition, 1,25(OH)(2)D-3 treatment promoted the nuclear accumulation of beta-catenin by downregulating BMP2. Furthermore, the beta-catenin signaling inhibitor XAV-939 weakened the inhibitory effect of 1,25(OH)(2)D-3 on osteogenic differentiation. Additionally, knockdown of beta-catenin rescued the attenuation in Dvl-1 and Smad1 interaction caused by 1,25(OH)(2)D-3. Overexpression of Smad1 also reversed the inhibitory effect of 1,25(OH)(2)D-3 on osteogenic differentiation. Taken together, the current study demonstrated that 1,25(OH)(2)D-3 inhibited the differentiation of BMSCs into osteoblast-like cells by inactivating BMP2 and activating Wnt/beta-catenin signaling.