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靶向miRNA-1247-5p的CircHmbox1参与肿瘤坏死因子-α对绝经后骨质疏松症骨代谢的调节

CircHmbox1 Targeting miRNA-1247-5p Is Involved in the Regulation of Bone Metabolism by TNF-α in Postmenopausal Osteoporosis.

作者信息

Liu Zhuochao, Li Changwei, Huang Ping, Hu Fangqiong, Jiang Min, Xu Xing, Li Bin, Deng Lianfu, Ye Tianwen, Guo Lei

机构信息

Department of Orthopedics, Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Shanghai Institute of Traumatology and Orthopedics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Orthopedic Surgery, Changzheng Hospital, Second Military Medical University, Shanghai, China.

出版信息

Front Cell Dev Biol. 2020 Dec 23;8:594785. doi: 10.3389/fcell.2020.594785. eCollection 2020.

Abstract

Tumor necrosis factor-alpha (TNF-α) promotes osteoclasts differentiation to enhance bone resorption and inhibits osteoblasts differentiation to impair bone formation, which plays a central role in the development of postmenopausal osteoporosis (PMOP). Recent studies implicated an important role of circular RNAs (circRNAs) in osteoporosis. The purpose of this study is to investigate whether circRNAs might be implicated in TNF-α-regulated osteoclasts differentiation and osteoblasts differentiation in PMOP. QRT-PCR was applied to detect expression of circRNA-circHmbox1 and miR-1247-5p in TNF-α-induced osteoclasts differentiation. Western blot, TRAP staining, alkaline phosphatase staining, alizarin red S staining, transwell and cell transfection were conducted to confirm that TNF-α inhibited osteoblasts differentiation by exosomal with low circHmbox1 expression from osteoclasts. Bioinformatics analysis and luciferase reporter revealed the mechanisms of the circHmbox1/miR-1247-5p/B cell lymphoma 6 (Bcl6) interaction. In this study, we found that the level of circRNA-circHmbox1 was obviously reduced in TNF-α-induced osteoclast formation and . CircHmbox1 could inhibit RANKL-induced osteoclasts differentiation primarily through binding to microRNA-1247-5p. TNF-α decreased osteoblasts differentiation by exosomal with low circHmbox1 expression from osteoclasts. Mechanistic studies showed that microRNA-1247-5p regulated osteoclasts differentiation and osteoblasts differentiation by targeting Bcl6, which was confirmed to play opposite roles in osteoblasts differentiation and osteoclasts differentiation. Our results provide evidence that circHmbox1-targeting miR-1247-5p is involved in the regulation of bone metabolisms by TNF-α in PMOP.

摘要

肿瘤坏死因子-α(TNF-α)促进破骨细胞分化以增强骨吸收,并抑制成骨细胞分化以损害骨形成,这在绝经后骨质疏松症(PMOP)的发展中起核心作用。最近的研究表明环状RNA(circRNAs)在骨质疏松症中起重要作用。本研究的目的是探讨circRNAs是否可能参与PMOP中TNF-α调节的破骨细胞分化和成骨细胞分化。应用QRT-PCR检测circRNA-circHmbox1和miR-1247-5p在TNF-α诱导的破骨细胞分化中的表达。进行蛋白质免疫印迹、抗酒石酸酸性磷酸酶染色、碱性磷酸酶染色、茜素红S染色、Transwell实验和细胞转染,以证实TNF-α通过来自破骨细胞的低circHmbox1表达的外泌体抑制成骨细胞分化。生物信息学分析和荧光素酶报告基因揭示了circHmbox1/miR-1247-5p/B细胞淋巴瘤6(Bcl6)相互作用的机制。在本研究中,我们发现circRNA-circHmbox1的水平在TNF-α诱导的破骨细胞形成中明显降低。CircHmbox1主要通过与微小RNA-1247-5p结合来抑制RANKL诱导的破骨细胞分化。TNF-α通过来自破骨细胞的低circHmbox1表达的外泌体降低成骨细胞分化。机制研究表明,微小RNA-1247-5p通过靶向Bcl6调节破骨细胞分化和成骨细胞分化,这被证实在成骨细胞分化和破骨细胞分化中起相反作用。我们的结果提供了证据,表明靶向circHmbox1的miR-1247-5p参与了PMOP中TNF-α对骨代谢的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e578/7786182/1cfd24c0890a/fcell-08-594785-g001.jpg

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