Suppr超能文献

miR-218 和 miR-618 在绝经后骨质疏松症中的作用。

The function of miR-218 and miR-618 in postmenopausal osteoporosis.

机构信息

Department of Obstetrics and Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

Eur Rev Med Pharmacol Sci. 2017 Dec;21(24):5534-5541. doi: 10.26355/eurrev_201712_13989.

Abstract

OBJECTIVE

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.

MATERIALS AND METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

材料和方法

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。

结果

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。

结论

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验