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Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration
MicroRNAs (miRNAs) can regulate the modulation of the phenotype of Schwann cells. Numerous novel miRNAs have been discovered and identified in rat sciatic nerve segments, including miR-3099. In the current study, miR-3099 expression levels following peripheral nerve injury were measured in the proxi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334613/ https://www.ncbi.nlm.nih.gov/pubmed/30539823 http://dx.doi.org/10.4103/1673-5374.245478 |
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author | Liu, Qian-Yan Miao, Yang Wang, Xing-Hui Wang, Pan Cheng, Zhang-Chun Qian, Tian-Mei |
author_facet | Liu, Qian-Yan Miao, Yang Wang, Xing-Hui Wang, Pan Cheng, Zhang-Chun Qian, Tian-Mei |
author_sort | Liu, Qian-Yan |
collection | PubMed |
description | MicroRNAs (miRNAs) can regulate the modulation of the phenotype of Schwann cells. Numerous novel miRNAs have been discovered and identified in rat sciatic nerve segments, including miR-3099. In the current study, miR-3099 expression levels following peripheral nerve injury were measured in the proximal stumps of rat sciatic nerves after surgical crush. Real-time reverse transcription-polymerase chain reaction was used to determine miR-3099 expression in the crushed nerve segment at 0, 1, 4, 7, and 14 days post sciatic nerve injury, which was consistent with Solexa sequencing outcomes. Expression of miR-3099 was up-regulated following peripheral nerve injury. EdU and transwell chamber assays were used to observe the effect of miR-3099 on Schwann cell proliferation and migration. The results showed that increased miR-3099 expression promoted the proliferation and migration of Schwann cells. However, reduced miR-3099 expression suppressed the proliferation and migration of Schwann cells. The potential target genes of miR-3099 were also investigated by bioinformatic tools and high-throughput outcomes. miR-3099 targets genes Aqp4, St8sia2, Tnfsf15, and Zbtb16 and affects the proliferation and migration of Schwann cells. This study examined the levels of miR-3099 at different time points following peripheral nerve injury. Our results confirmed that increased miR-3099 level induced by peripheral nerve injury can promote the proliferation and migration of Schwann cells. |
format | Online Article Text |
id | pubmed-6334613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63346132019-03-01 Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration Liu, Qian-Yan Miao, Yang Wang, Xing-Hui Wang, Pan Cheng, Zhang-Chun Qian, Tian-Mei Neural Regen Res Research Article MicroRNAs (miRNAs) can regulate the modulation of the phenotype of Schwann cells. Numerous novel miRNAs have been discovered and identified in rat sciatic nerve segments, including miR-3099. In the current study, miR-3099 expression levels following peripheral nerve injury were measured in the proximal stumps of rat sciatic nerves after surgical crush. Real-time reverse transcription-polymerase chain reaction was used to determine miR-3099 expression in the crushed nerve segment at 0, 1, 4, 7, and 14 days post sciatic nerve injury, which was consistent with Solexa sequencing outcomes. Expression of miR-3099 was up-regulated following peripheral nerve injury. EdU and transwell chamber assays were used to observe the effect of miR-3099 on Schwann cell proliferation and migration. The results showed that increased miR-3099 expression promoted the proliferation and migration of Schwann cells. However, reduced miR-3099 expression suppressed the proliferation and migration of Schwann cells. The potential target genes of miR-3099 were also investigated by bioinformatic tools and high-throughput outcomes. miR-3099 targets genes Aqp4, St8sia2, Tnfsf15, and Zbtb16 and affects the proliferation and migration of Schwann cells. This study examined the levels of miR-3099 at different time points following peripheral nerve injury. Our results confirmed that increased miR-3099 level induced by peripheral nerve injury can promote the proliferation and migration of Schwann cells. Medknow Publications & Media Pvt Ltd 2019-03 /pmc/articles/PMC6334613/ /pubmed/30539823 http://dx.doi.org/10.4103/1673-5374.245478 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 Liu, Qian-Yan Miao, Yang Wang, Xing-Hui Wang, Pan Cheng, Zhang-Chun Qian, Tian-Mei Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration |
title | Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration |
title_full | Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration |
title_fullStr | Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration |
title_full_unstemmed | Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration |
title_short | Increased levels of miR-3099 induced by peripheral nerve injury promote Schwann cell proliferation and migration |
title_sort | increased levels of mir-3099 induced by peripheral nerve injury promote schwann cell proliferation and migration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6334613/ https://www.ncbi.nlm.nih.gov/pubmed/30539823 http://dx.doi.org/10.4103/1673-5374.245478 |
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