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Long non-coding RNA-DANCR in human circulating monocytes: a potential biomarker associated with postmenopausal osteoporosis

机译:人循环单核细胞中长的非编码RNA-DANCR:与绝经后骨质疏松症相关的潜在生物标志物

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摘要

Osteoporosis is a common disease characterized by low bone mineral density (BMD) and low trauma fractures, mainly resulting from exceeding bone resorption by osteoclasts over bone formation by osteoblasts. Circulating monocytes are directly involved in osteoclastogenesis, and lncRNAs are believed to be involved in the osteoblast differentiation. However, no study has been conducted to identify the roles of lncRNA in circulating monocytes associated with human osteoporosis. In this study, we found significant upregulation of DANCR in the blood mononuclear cells (MNCs) from low-BMD patients with the qRT-PCR analyses. We further found that DANCR promoted the expression of IL6 and TNF-alpha at both mRNA level and protein level in MNCs. After deletion of DANCR with siRNAs, the levels of IL6 and TNF-alpha are decreased in the MNCs from low-BMD postmenopausal women. Moreover, DANCR level was correlated with IL6 and TNF-alpha in postmenopausal women with low BMD. Furthermore, we found that DANCR-induced IL6 and TNF-alpha in MNCs had bone-resorbing activity. These results indicate that DANCR is involved in the pathology of osteoporosis and may be as a biomarker for postmenopausal osteoporosis.
机译:骨质疏松症是一种常见的疾病,其特征在于骨矿物密度低(BMD)和低创伤骨折,主要导致骨细胞通过成骨细胞的骨形成超过骨细胞的重吸收。循环单核细胞直接参与骨核细胞发生,并且据信LNCRNA参与成骨细胞分化。然而,未进行研究以确定LNCRNA在与人骨质疏松症相关的循环单核细胞中的作用。在这项研究中,我们发现,来自低BMD患者的QRT-PCR分析的血液单核细胞(MNC)中的DANCR显着上调。我们进一步发现,DANCR在MNC中促进了MRNA水平和蛋白质水平的IL6和TNF-α表达。用siRNA删除DANCR后,IL6和TNF-α的水平在低BMD绝经后妇女的MNC中降低。此外,DANCR水平与低BMD的绝经后妇女中的IL6和TNF-α相关。此外,我们发现丹佛诱导的IL6和MNC中的TNF-α具有骨再吸收活性。这些结果表明,DANCR参与了骨质疏松症的病理学,并且可以作为绝经后骨质疏松症的生物标志物。

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