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LncRNA PVT1 Regulates Chondrocyte Apoptosis in Osteoarthritis by Acting as a Sponge for miR-488-3p

机译:LNCRNA PVT1通过作为MIR-488-3P的海绵调节骨关节炎的软骨细胞凋亡

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摘要

Long noncoding RNAs (lncRNAs) have been known to be involved in multiple diverse diseases, including osteoarthritis (OA). The present study aims at exploring the biological role of lncRNA plasmacytoma variant translocation 1 (PVT1) in OA and the underlying mechanism. Results showed that the expression of PVT1 was upregulated in OA chondrocytes compared with normal chondrocytes, silencing PVT1 inhibited the apoptosis of OA chondrocytes, and overexpression of PVT1 promoted the apoptosis of normal chondrocytes. To further investigate the underlying mechanism, miR-488-3p was predicted to be a targeted microRNA of PVT1. Different methods, including MS2 RNA immunoprecipitation (RIP), luciferase activity, and anti-AGO2 RIP, were performed to detect the interaction between PVT1 and miR-488-3p, which suggested that PVT1 negatively regulated miR-488-3p in OA chondrocytes. Moreover, PVT1 promoted the apoptosis of OA and normal chondrocytes through miR-488-3p. Collectively, this study revealed that lncRNA PVT1 regulated the apoptosis of chondrocytes by acting as a sponge for miR-488-3p in OA. PVT1 may be considered a new therapeutic target for the treatment of OA.
机译:已知长期非编码RNA(LNCRNA)参与多种不同的疾病,包括骨关节炎(OA)。本研究旨在探讨液体和潜在机制中LNCRNA血浆浆瘤变异易位1(PVT1)的生物学作用。结果表明,与正常软骨细胞相比,在OA软骨细胞中升高了PVT1的表达,沉默PVT1抑制了OA软骨细胞的凋亡,PVT1的过表达促进了正常软骨细胞的凋亡。为了进一步研究潜在的机制,预测MIR-488-3P是PVT1的靶向microRNA。进行不同的方法,包括MS2 RNA免疫沉积件(RIP),荧光素酶活性和抗Agay2 RIP,以检测PVT1和MIR-488-3P之间的相互作用,这表明PVT1在OA软骨细胞中对miR-488-3P负调节。此外,PVT1通过MIR-488-3P促进OA和正常软骨细胞的凋亡。集体,本研究表明,LNCRNA PVT1通过用作OA中的miR-488-3p的海绵来调节软骨细胞的凋亡。 PVT1可被认为是治疗OA的新治疗靶标。

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