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长链非编码RNA Pvt1通过在外周神经损伤后海绵化微小RNA-214并靶向c-Jun来促进雪旺细胞的增殖和迁移。

Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury.

作者信息

Pan Bin, Guo Di, Jing Li, Li Ke, Li Xin, Li Gen, Gao Xiao, Li Zhi-Wen, Zhao Wei, Feng Hu, Cao Meng-Han

机构信息

Department of Orthopedics, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.

Department of Orthopedics, The Second Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu Province, China.

出版信息

Neural Regen Res. 2023 May;18(5):1147-1153. doi: 10.4103/1673-5374.353497.

Abstract

Research has shown that long-chain noncoding RNAs (lncRNAs) are involved in the regulation of a variety of biological processes, including peripheral nerve regeneration, in part by acting as competing endogenous RNAs. c-Jun plays a key role in the repair of peripheral nerve injury. However, the precise underlying mechanism of c-Jun remains unclear. In this study, we performed microarray and bioinformatics analysis of mouse crush-injured sciatic nerves and found that the lncRNA Pvt1 was overexpressed in Schwann cells after peripheral nerve injury. Mechanistic studies revealed that Pvt1 increased c-Jun expression through sponging miRNA-214. We overexpressed Pvt1 in Schwann cells cultured in vitro and found that the proliferation and migration of Schwann cells were enhanced, and overexpression of miRNA-214 counteracted the effects of Pvt1 overexpression on Schwann cell proliferation and migration. We conducted in vivo analyses and injected Schwann cells overexpressing Pvt1 into injured sciatic nerves of mice. Schwann cells overexpressing Pvt1 enhanced the regeneration of injured sciatic nerves following peripheral nerve injury and the locomotor function of mice was improved. Our findings reveal the role of lncRNAs in the repair of peripheral nerve injury and highlight lncRNA Pvt1 as a novel potential treatment target for peripheral nerve injury.

摘要

研究表明,长链非编码RNA(lncRNA)参与多种生物过程的调控,包括外周神经再生,部分是通过作为竞争性内源性RNA发挥作用。c-Jun在外周神经损伤修复中起关键作用。然而,c-Jun的确切潜在机制仍不清楚。在本研究中,我们对小鼠挤压损伤的坐骨神经进行了微阵列和生物信息学分析,发现lncRNA Pvt1在外周神经损伤后在雪旺细胞中过表达。机制研究表明,Pvt1通过吸附miRNA-214增加c-Jun的表达。我们在体外培养的雪旺细胞中过表达Pvt1,发现雪旺细胞的增殖和迁移增强,而miRNA-

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b56d/9827779/571c78a32502/NRR-18-1147-g002.jpg

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