成骨细胞
运行x2
间充质干细胞
化学
下调和上调
小RNA
碱性磷酸酶
污渍
细胞生物学
报告基因
分子生物学
细胞分化
基因表达
生物化学
基因
生物
体外
酶
作者
Qiting He,Hengshuo Zhang,Beibei Hu,Xuezhou Li,Yunpeng Wu,Pengfei Sun,Yuhua Jia,Lei Cheng,Yongyuan Guo
标识
DOI:10.1016/j.bej.2022.108386
摘要
Human adipose mesenchymal stem cells (hAMSCs) can differentiate into osteoblasts, which can enhance bone mass and bone formation. Circular RNA plays an important role in the osteoblast differentiation of mesenchymal stem cells, but the mechanism remains unclear. We used hAMSCs to study the role of circRNA hsa_circ_0001421/miR-608/SP7 axis in osteoblast differentiation. qRT-PCR, western blotting, alkaline phosphatase (ALP) activity measurement, and alizarin red staining (ARS) were used to evaluate the osteoblast differentiation ability of hAMSCs. Dual luciferase reporter gene assay to analyze the relationship of miR-608 with circRNA hsa_circ_0001421 and SP7. Our results showed that circRNA hsa_circ_0001421 could promote the osteoblast differentiation of hAMSCs. qRT-PCR and western blotting showed that the expression of osteogenic genes (ALP, RUNX2, and OCN) was upregulated, and ALP activity and ARS were significantly increased. The dual luciferase reporter gene assay showed that miR-608 competitively binds with circRNA hsa_circ_0001421 and SP7. MiR-608 inhibited the expression of SP7 and repressed the osteoblast differentiation of hAMSCs, whereas circRNA hsa_circ_0001421 inhibited the expression of miR-608 and reversed the downregulation of SP7 by miR-608. Taken together, the circRNA hsa_circ_0001421/miR-608/SP7 axis at least partially regulates the osteoblast differentiation of hAMSCs, which may be a potential target of hAMSCs for the treatment of osteoporosis.
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