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MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42
OBJECTIVE: Neural stem cells play an important role in the recovery and regeneration of peripheral nerve injury, and the microRNA-7 (miR-7) regulates differentiation of neural stem cells. This study aimed to explore the role of miR-7 in neural stem cells homing and proliferation and its influence on...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5912295/ https://www.ncbi.nlm.nih.gov/pubmed/29663842 http://dx.doi.org/10.1177/1744806918766793 |
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author | Zhou, Nan Hao, Shuang Huang, Zongqiang Wang, Weiwei Yan, Penghui Zhou, Wei Zhu, Qihang Liu, Xiaokang |
author_facet | Zhou, Nan Hao, Shuang Huang, Zongqiang Wang, Weiwei Yan, Penghui Zhou, Wei Zhu, Qihang Liu, Xiaokang |
author_sort | Zhou, Nan |
collection | PubMed |
description | OBJECTIVE: Neural stem cells play an important role in the recovery and regeneration of peripheral nerve injury, and the microRNA-7 (miR-7) regulates differentiation of neural stem cells. This study aimed to explore the role of miR-7 in neural stem cells homing and proliferation and its influence on peripheral nerve injury repair. METHODS: The mice model of peripheral nerve injury was created by segmental sciatic nerve defect (sciatic nerve injury), and neural stem cells treatment was performed with a gelatin hydrogel conduit containing neural stem cells inserted into the sciatic nerve injury mice. The Sciatic Function Index was used to quantify sciatic nerve functional recovery in the mice. The messenger RNA and protein expression were detected by reverse transcription polymerase chain reaction and Western blot, respectively. Luciferase reporter assay was used to confirm the binding between miR-7 and the 3’UTR of cell division cycle protein 42 (cdc42). The neural stem cells migration and proliferation were analyzed by transwell assay and a Cell-LightTM EdU DNA Cell Proliferation kit, respectively. RESULTS: Neural stem cells treatment significantly promoted nerve repair in sciatic nerve injury mice. MiR-7 expression was decreased in sciatic nerve injury mice with neural stem cells treatment, and miR-7 mimic transfected into neural stem cells suppressed migration and proliferation, while miR-7 inhibitor promoted migration and proliferation. The expression level and effect of cdc42 on neural stem cells migration and proliferation were opposite to miR-7, and the luciferase reporter assay proved that cdc42 was a target of miR-7. Using co-transfection into neural stem cells, we found pcDNA3.1-cdc42 and si-cdc42 could reverse respectively the role of miR-7 mimic and miR-7 inhibitor on neural stem cells migration and proliferation. In addition, miR-7 mimic-transfected neural stem cells could abolish the protective role of neural stem cells on peripheral nerve injury. CONCLUSION: MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42. |
format | Online Article Text |
id | pubmed-5912295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-59122952018-04-27 MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 Zhou, Nan Hao, Shuang Huang, Zongqiang Wang, Weiwei Yan, Penghui Zhou, Wei Zhu, Qihang Liu, Xiaokang Mol Pain Research Article OBJECTIVE: Neural stem cells play an important role in the recovery and regeneration of peripheral nerve injury, and the microRNA-7 (miR-7) regulates differentiation of neural stem cells. This study aimed to explore the role of miR-7 in neural stem cells homing and proliferation and its influence on peripheral nerve injury repair. METHODS: The mice model of peripheral nerve injury was created by segmental sciatic nerve defect (sciatic nerve injury), and neural stem cells treatment was performed with a gelatin hydrogel conduit containing neural stem cells inserted into the sciatic nerve injury mice. The Sciatic Function Index was used to quantify sciatic nerve functional recovery in the mice. The messenger RNA and protein expression were detected by reverse transcription polymerase chain reaction and Western blot, respectively. Luciferase reporter assay was used to confirm the binding between miR-7 and the 3’UTR of cell division cycle protein 42 (cdc42). The neural stem cells migration and proliferation were analyzed by transwell assay and a Cell-LightTM EdU DNA Cell Proliferation kit, respectively. RESULTS: Neural stem cells treatment significantly promoted nerve repair in sciatic nerve injury mice. MiR-7 expression was decreased in sciatic nerve injury mice with neural stem cells treatment, and miR-7 mimic transfected into neural stem cells suppressed migration and proliferation, while miR-7 inhibitor promoted migration and proliferation. The expression level and effect of cdc42 on neural stem cells migration and proliferation were opposite to miR-7, and the luciferase reporter assay proved that cdc42 was a target of miR-7. Using co-transfection into neural stem cells, we found pcDNA3.1-cdc42 and si-cdc42 could reverse respectively the role of miR-7 mimic and miR-7 inhibitor on neural stem cells migration and proliferation. In addition, miR-7 mimic-transfected neural stem cells could abolish the protective role of neural stem cells on peripheral nerve injury. CONCLUSION: MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42. SAGE Publications 2018-04-17 /pmc/articles/PMC5912295/ /pubmed/29663842 http://dx.doi.org/10.1177/1744806918766793 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Zhou, Nan Hao, Shuang Huang, Zongqiang Wang, Weiwei Yan, Penghui Zhou, Wei Zhu, Qihang Liu, Xiaokang MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 |
title | MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 |
title_full | MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 |
title_fullStr | MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 |
title_full_unstemmed | MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 |
title_short | MiR-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 |
title_sort | mir-7 inhibited peripheral nerve injury repair by affecting neural stem cells migration and proliferation through cdc42 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5912295/ https://www.ncbi.nlm.nih.gov/pubmed/29663842 http://dx.doi.org/10.1177/1744806918766793 |
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