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Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration

MicroRNAs refer to a class of endogenous, short non-coding RNAs that mediate numerous biological functions. MicroRNAs regulate various physiological and pathological activities of peripheral nerves, including peripheral nerve repair and regeneration. Previously, using a rat sciatic nerve injury mode...

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Autores principales: Ji, Xi-Meng, Wang, Shan-Shan, Cai, Xiao-Dong, Wang, Xing-Hui, Liu, Qian-Yan, Wang, Pan, Cheng, Zhang-Chun, Qian, Tian-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557103/
https://www.ncbi.nlm.nih.gov/pubmed/31089066
http://dx.doi.org/10.4103/1673-5374.255996
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author Ji, Xi-Meng
Wang, Shan-Shan
Cai, Xiao-Dong
Wang, Xing-Hui
Liu, Qian-Yan
Wang, Pan
Cheng, Zhang-Chun
Qian, Tian-Mei
author_facet Ji, Xi-Meng
Wang, Shan-Shan
Cai, Xiao-Dong
Wang, Xing-Hui
Liu, Qian-Yan
Wang, Pan
Cheng, Zhang-Chun
Qian, Tian-Mei
author_sort Ji, Xi-Meng
collection PubMed
description MicroRNAs refer to a class of endogenous, short non-coding RNAs that mediate numerous biological functions. MicroRNAs regulate various physiological and pathological activities of peripheral nerves, including peripheral nerve repair and regeneration. Previously, using a rat sciatic nerve injury model, we identified many functionally annotated novel microRNAs, including miR-sc14. Here, we used real-time reverse transcription-polymerase chain reaction to examine miR-sc14 expression in rat sciatic nerve stumps. Our results show that miR-sc14 is noticeably altered following sciatic nerve injury, being up-regulated at 1 day and diminished at 7 days. EdU and transwell chamber assay results showed that miR-sc14 mimic promoted proliferation and migration of Schwann cells, while miR-sc14 inhibitor suppressed their proliferation and migration. Additionally, bioinformatic analysis examined potential target genes of miR-sc14, and found that fibroblast growth factor receptor 2 might be a potential target gene. Specifically, our results show changes of miR-sc14 expression in the sciatic nerve of rats at different time points after nerve injury. Appropriately, up-regulation of miR-sc14 promoted proliferation and migration of Schwann cells. Consequently, miR-sc14 may be an intervention target to promote repair of peripheral nerve injury. The study was approved by the Jiangsu Provincial Laboratory Animal Management Committee, China on March 4, 2015 (approval No. 20150304-004).
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spelling pubmed-65571032019-09-01 Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration Ji, Xi-Meng Wang, Shan-Shan Cai, Xiao-Dong Wang, Xing-Hui Liu, Qian-Yan Wang, Pan Cheng, Zhang-Chun Qian, Tian-Mei Neural Regen Res Research Article MicroRNAs refer to a class of endogenous, short non-coding RNAs that mediate numerous biological functions. MicroRNAs regulate various physiological and pathological activities of peripheral nerves, including peripheral nerve repair and regeneration. Previously, using a rat sciatic nerve injury model, we identified many functionally annotated novel microRNAs, including miR-sc14. Here, we used real-time reverse transcription-polymerase chain reaction to examine miR-sc14 expression in rat sciatic nerve stumps. Our results show that miR-sc14 is noticeably altered following sciatic nerve injury, being up-regulated at 1 day and diminished at 7 days. EdU and transwell chamber assay results showed that miR-sc14 mimic promoted proliferation and migration of Schwann cells, while miR-sc14 inhibitor suppressed their proliferation and migration. Additionally, bioinformatic analysis examined potential target genes of miR-sc14, and found that fibroblast growth factor receptor 2 might be a potential target gene. Specifically, our results show changes of miR-sc14 expression in the sciatic nerve of rats at different time points after nerve injury. Appropriately, up-regulation of miR-sc14 promoted proliferation and migration of Schwann cells. Consequently, miR-sc14 may be an intervention target to promote repair of peripheral nerve injury. The study was approved by the Jiangsu Provincial Laboratory Animal Management Committee, China on March 4, 2015 (approval No. 20150304-004). Wolters Kluwer - Medknow 2019-09 /pmc/articles/PMC6557103/ /pubmed/31089066 http://dx.doi.org/10.4103/1673-5374.255996 Text en Copyright: © Neural Regeneration Research http://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
Ji, Xi-Meng
Wang, Shan-Shan
Cai, Xiao-Dong
Wang, Xing-Hui
Liu, Qian-Yan
Wang, Pan
Cheng, Zhang-Chun
Qian, Tian-Mei
Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration
title Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration
title_full Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration
title_fullStr Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration
title_full_unstemmed Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration
title_short Novel miRNA, miR-sc14, promotes Schwann cell proliferation and migration
title_sort novel mirna, mir-sc14, promotes schwann cell proliferation and migration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557103/
https://www.ncbi.nlm.nih.gov/pubmed/31089066
http://dx.doi.org/10.4103/1673-5374.255996
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