Department of Obstetrics and Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Eur Rev Med Pharmacol Sci. 2017 Dec;21(24):5534-5541. doi: 10.26355/eurrev_201712_13989.
Postmenopausal osteoporosis (POMP) is a serious disorder with significant physical, psychosocial, and financial consequences, which greatly reduce the postmenopausal women's life quality. The related issues of postmenopausal osteoporosis are increasingly concerned by society. Past researches have shown that miRNAs play an important role in the occurrence and development of postmenopausal osteoporosis. However, the role of miR-218 and miR-618 in the osteoporosis regulation is still unclear.
First of all, we investigated the alteration of miR-218 and miR-618 during osteoclastogenesis of RAW264.7 cells. Next, we transfected RAW264.7 cells with miR-218 or miR-618 mimics and inhibitors to explore the influences of miR-218 and miR-618 on osteoclast differentiation. Then, we conducted bioinformatics analysis and luciferase reporter assay to identify and test the target gene of miR-218 and miR-618.
MiR-218 and miR-618 were down-regulated when RAW264.7 cells differentiated into osteoclasts. In addition, overexpression of miR-218 or miR-618 attenuated RAW264.7 cells differentiated into osteoclasts in vitro, whereas inhibition of miR-218 or miR-618 promoted this progress. This was demonstrated by increased expression of osteoclast-specific genes and TRAP staining. TLR-4 was confirmed to be the direct target of miR-218 and miR-618 by bioinformatics and luciferase reporter assay.
These results suggested that miR-218 and miR-618 play an important role in osteoclastogenesis via TLR-4/MyD88/NF-κB signaling pathway. Thus, targeting miR-218 and miR-618 promise a therapeutic potential in the treatment of osteoporosis.
绝经后骨质疏松症(POMP)是一种严重的疾病,具有显著的身体、心理社会和经济后果,极大地降低了绝经后妇女的生活质量。与绝经后骨质疏松症相关的问题越来越受到社会的关注。过去的研究表明,miRNA 在绝经后骨质疏松症的发生和发展中起重要作用。然而,miR-218 和 miR-618 在骨质疏松症调节中的作用尚不清楚。
首先,我们研究了 miR-218 和 miR-618 在 RAW264.7 细胞破骨细胞分化过程中的变化。接下来,我们用 miR-218 或 miR-618 模拟物和抑制剂转染 RAW264.7 细胞,以探讨 miR-218 和 miR-618 对破骨细胞分化的影响。然后,我们进行了生物信息学分析和荧光素酶报告基因检测,以鉴定和测试 miR-218 和 miR-618 的靶基因。
当 RAW264.7 细胞分化为破骨细胞时,miR-218 和 miR-618 下调。此外,miR-218 或 miR-618 的过表达在体外抑制了 RAW264.7 细胞分化为破骨细胞,而 miR-218 或 miR-618 的抑制促进了这一进程。这可以通过增加破骨细胞特异性基因的表达和 TRAP 染色来证明。生物信息学和荧光素酶报告基因检测证实 TLR-4 是 miR-218 和 miR-618 的直接靶基因。
这些结果表明,miR-218 和 miR-618 通过 TLR-4/MyD88/NF-κB 信号通路在破骨细胞分化中发挥重要作用。因此,针对 miR-218 和 miR-618 有望成为治疗骨质疏松症的一种治疗潜力。