成骨细胞
骨钙素
小RNA
同源盒
碱性磷酸酶
Hox基因
C2C12型
化学
免疫印迹
细胞生物学
细胞分化
分子生物学
基因表达
生物
基因
生物化学
体外
酶
肌发生
作者
Jian Yin,Xiao Wei,Qingbin Zhao,Jungang Sun,Wenzheng Zhou,Wei Zhao
标识
DOI:10.1080/08923973.2022.2052895
摘要
Objective Recent studies have demonstrated that micro RNAs (miRNAs) are involved in bone formation and bone cell differentiation, but the role of miR-582-3p in osteoporosis is unclear. We want to study the mechanism of miR-582-3p on osteogenic differentiation.Method The expression of miR-582-3p and homeobox (Hox) A10 were analyzed by quantitative RT-PCR. The expression levels of HOXA10 protein were determined by Western blot. The target of HOXA10 was identified by bioinformatics and luciferase reporter gene assay.Results The results showed that miR-582-3p was up-regulated in OP tissues and down-regulated in osteogenic differentiated C2C12 cells compared with that in the control group. Overexpression of miR-582-3p resulted in reduced expression levels of osteocalcin (OC), alkaline phosphatase (ALP), and collagen, type I, α1 (COL1A1). miR-582-3p had a potential binding site with HOXA10. Moreover, miR-582-3p inhibited the expression of HOXA10, and overexpression of HOXA10 reduced the effect of miR-582-3p on osteoblast markers. HOXA10 was the target gene of miR-582-3p, which could inhibit the expression of HOXA10. Furthermore, HOXA10 reduced the role of miR-582-3p in osteoblast markers. miR-582-3p inhibited the development of osteoporosis by regulating HOXA10 and osteoblast differentiation.Conclusions miR-582-3p may be a therapeutic target of osteoporosis treatment.
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