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

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 prec...

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Autores principales: Pan, Bin, Guo, Di, Jing, Li, Li, Ke, Li, Xin, Li, Gen, Gao, Xiao, Li, Zhi-Wen, Zhao, Wei, Feng, Hu, Cao, Meng-Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827779/
https://www.ncbi.nlm.nih.gov/pubmed/36255005
http://dx.doi.org/10.4103/1673-5374.353497
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author Pan, Bin
Guo, Di
Jing, Li
Li, Ke
Li, Xin
Li, Gen
Gao, Xiao
Li, Zhi-Wen
Zhao, Wei
Feng, Hu
Cao, Meng-Han
author_facet Pan, Bin
Guo, Di
Jing, Li
Li, Ke
Li, Xin
Li, Gen
Gao, Xiao
Li, Zhi-Wen
Zhao, Wei
Feng, Hu
Cao, Meng-Han
author_sort Pan, Bin
collection PubMed
description 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.
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spelling pubmed-98277792023-01-10 Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury Pan, Bin Guo, Di Jing, Li Li, Ke Li, Xin Li, Gen Gao, Xiao Li, Zhi-Wen Zhao, Wei Feng, Hu Cao, Meng-Han Neural Regen Res Research Article 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. Wolters Kluwer - Medknow 2022-10-10 /pmc/articles/PMC9827779/ /pubmed/36255005 http://dx.doi.org/10.4103/1673-5374.353497 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Pan, Bin
Guo, Di
Jing, Li
Li, Ke
Li, Xin
Li, Gen
Gao, Xiao
Li, Zhi-Wen
Zhao, Wei
Feng, Hu
Cao, Meng-Han
Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury
title Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury
title_full Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury
title_fullStr Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury
title_full_unstemmed Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury
title_short Long noncoding RNA Pvt1 promotes the proliferation and migration of Schwann cells by sponging microRNA-214 and targeting c-Jun following peripheral nerve injury
title_sort long noncoding rna pvt1 promotes the proliferation and migration of schwann cells by sponging microrna-214 and targeting c-jun following peripheral nerve injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827779/
https://www.ncbi.nlm.nih.gov/pubmed/36255005
http://dx.doi.org/10.4103/1673-5374.353497
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