College of Life Sciences, Shandong Agricultural University, Tai'an 271018, China.
College of Life Sciences, Shandong Agricultural University, Tai'an 271018, China
Biosci Rep. 2018 Jun 27;38(3). doi: 10.1042/BSR20171618. Print 2018 Jun 29.
In the present study, we explored the role of the interferon-inducible protein p202 in osteoblast differentiation of mouse bone marrow stromal cells (BMSCs). Both the mRNA and protein levels of p202 increased initially and decreased afterward in the course of BMSC osteogenesis. The intracellular distribution of this protein also changed in the differentiation process. p202 knockdown inhibited, while p202 overexpression enhanced, the osteoblast differentiation of BMSCs. This was identified by evaluation of expression of osteogenic markers, Alizarin Red S staining, and determination of alkaline phosphatase activity. Further study revealed that p202 disturbs the formation of Runx2/Ids complex and frees Runx2 to induce the differentiation process. The findings demonstrated that p202 plays a positive role in BMSC osteogenesis.
在本研究中,我们探讨了干扰素诱导蛋白 p202 在小鼠骨髓基质细胞(BMSC)成骨分化中的作用。在 BMSC 成骨过程中,p202 的 mRNA 和蛋白水平最初升高,随后降低。该蛋白的细胞内分布在分化过程中也发生了变化。p202 敲低抑制,而 p202 过表达增强,BMSC 的成骨分化。这是通过评估成骨标志物的表达、茜素红 S 染色和碱性磷酸酶活性来确定的。进一步的研究表明,p202 干扰 Runx2/Ids 复合物的形成并释放 Runx2 以诱导分化过程。研究结果表明,p202 在 BMSC 成骨中发挥积极作用。