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首页> 外文期刊>Frontiers in Cell and Developmental Biology >CircHmbox1 Targeting miRNA-1247-5p Is Involved in the Regulation of Bone Metabolism by TNF-α in Postmenopausal Osteoporosis
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CircHmbox1 Targeting miRNA-1247-5p Is Involved in the Regulation of Bone Metabolism by TNF-α in Postmenopausal Osteoporosis

机译:靶向miRNA-1247-5P的Circhmbox1参与通过绝经后骨质疏松症的TNF-α对骨代谢的调节

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Tumor necrosis factor-alpha (TNF-α) increases osteoclasts differentiation to enhance bone resorption and inhibits osteoblasts differentiation to impair bone formation, which play a central role in the pathogenesis 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 performed 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 the exosomal with low circHmbox1 expression from osteoclasts. Bioinformatics analysis and luciferase reporter were used to reveal the mechanisms of the circHmbox1/miR-1247-5p/Bcl6 interaction. In this study, we found that the level of circRNA-circHmbox1 was obviously decreased in the induction of osteoclasts differentiation by TNF-α in vivo and in vitro. CircHmbox1 could inhibit RANKL-induced osteoclasts differentiation primarily through binding to microRNA-1247-5p. TNF-α decreased osteoblasts differentiation by the exosomal with low circHmbox1 expression from osteoclasts. Mechanistic studies showed that microRNA-1247-5p regulated osteoclasts differentiation and osteoblasts differentiation by targeting B cell lymphoma 6, 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.
机译:肿瘤坏死因子 - α(TNF-α)增加了骨细胞分化以增强骨吸收,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)的发病机制中起着重要作用。最近的研究涉及圆形RNA(Circrnas)在骨质疏松症中的重要作用。本研究的目的是研究CircrNA是否可能涉及在PMOP中的TNF-α-调节的骨酸分化和成骨细胞分化中。进行QRT-PCR以检测TNF-α诱导的破骨细胞分化中CircrNA-Circhmbox1和miR-1247-5p的表达。进行蛋白质印迹,捕获染色,碱性磷酸酶染色,茜素红S染色,Transwell和细胞转染,以确认TNF-α通过疏松骨细胞的低circhmbox1表达抑制Exosomal的成骨细胞分化。生物信息学分析和荧光素酶报告者用于揭示Circhmbox1 / miR-1247-5p / bcl6相互作用的机制。在这项研究中,我们发现Circrna-circhmbox1的水平在体内和体外TNF-α的诱导分化中显然降低。 Circhmbox1可以抑制RANKL诱导的骨核苷酸分化,主要通过结合MicroRNA-1247-5P。 TNF-α通过疏口细胞的低circhmbox1表达降低了外泌素细胞分化。机械研究表明,通过靶向B细胞淋巴瘤6,MICRRNA-1247-5P调节的骨壳分化和成骨细胞分化,其证实在成骨细胞分化和疏口细胞分化中起相反的作用。我们的结果提供了Circhmbox1靶向miR-1247-5p的证据,参与了PMOP中TNF-α对骨代谢的调节。

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