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Circ-Spidr enhances axon regeneration after peripheral nerve injury
Accumulating evidence suggests that circular RNAs (circRNAs) are abundant and play critical roles in the nervous system. However, their functions in axon regeneration after neuronal injury are unclear. Due to its robust regeneration capacity, peripheral nervous system is ideal for seeking the regula...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797756/ https://www.ncbi.nlm.nih.gov/pubmed/31624232 http://dx.doi.org/10.1038/s41419-019-2027-x |
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author | Mao, Susu Huang, Tao Chen, Yuanyuan Shen, Longxiang Zhou, Shuoshuo Zhang, Shanshan Yu, Bin |
author_facet | Mao, Susu Huang, Tao Chen, Yuanyuan Shen, Longxiang Zhou, Shuoshuo Zhang, Shanshan Yu, Bin |
author_sort | Mao, Susu |
collection | PubMed |
description | Accumulating evidence suggests that circular RNAs (circRNAs) are abundant and play critical roles in the nervous system. However, their functions in axon regeneration after neuronal injury are unclear. Due to its robust regeneration capacity, peripheral nervous system is ideal for seeking the regulatory circRNAs in axon regeneration. In the present work, we obtained an expression profile of circRNAs in dorsal root ganglions (DRGs) after rat sciatic nerve crush injury by RNA sequencing (RNA-Seq) and found the expression level of circ-Spidr was obviously increased using quantitative real-time polymerase chain reaction (qRT-PCR). Furthermore, circ-Spidr was proved to be a circular RNA enriched in the cytoplasm of DRG neurons. Through in vitro and in vivo experiments, we determined that down-regulation of circ-Spidr could suppress axon regeneration of DRG neurons after sciatic nerve injury partially through modulating PI3K-Akt signaling pathway. Together, our results reveal a crucial role for circRNAs in regulating axon regeneration after neuronal injury which may further serve as a potential therapeutic avenue for neuronal injury repair. |
format | Online Article Text |
id | pubmed-6797756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67977562019-10-18 Circ-Spidr enhances axon regeneration after peripheral nerve injury Mao, Susu Huang, Tao Chen, Yuanyuan Shen, Longxiang Zhou, Shuoshuo Zhang, Shanshan Yu, Bin Cell Death Dis Article Accumulating evidence suggests that circular RNAs (circRNAs) are abundant and play critical roles in the nervous system. However, their functions in axon regeneration after neuronal injury are unclear. Due to its robust regeneration capacity, peripheral nervous system is ideal for seeking the regulatory circRNAs in axon regeneration. In the present work, we obtained an expression profile of circRNAs in dorsal root ganglions (DRGs) after rat sciatic nerve crush injury by RNA sequencing (RNA-Seq) and found the expression level of circ-Spidr was obviously increased using quantitative real-time polymerase chain reaction (qRT-PCR). Furthermore, circ-Spidr was proved to be a circular RNA enriched in the cytoplasm of DRG neurons. Through in vitro and in vivo experiments, we determined that down-regulation of circ-Spidr could suppress axon regeneration of DRG neurons after sciatic nerve injury partially through modulating PI3K-Akt signaling pathway. Together, our results reveal a crucial role for circRNAs in regulating axon regeneration after neuronal injury which may further serve as a potential therapeutic avenue for neuronal injury repair. Nature Publishing Group UK 2019-10-17 /pmc/articles/PMC6797756/ /pubmed/31624232 http://dx.doi.org/10.1038/s41419-019-2027-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mao, Susu Huang, Tao Chen, Yuanyuan Shen, Longxiang Zhou, Shuoshuo Zhang, Shanshan Yu, Bin Circ-Spidr enhances axon regeneration after peripheral nerve injury |
title | Circ-Spidr enhances axon regeneration after peripheral nerve injury |
title_full | Circ-Spidr enhances axon regeneration after peripheral nerve injury |
title_fullStr | Circ-Spidr enhances axon regeneration after peripheral nerve injury |
title_full_unstemmed | Circ-Spidr enhances axon regeneration after peripheral nerve injury |
title_short | Circ-Spidr enhances axon regeneration after peripheral nerve injury |
title_sort | circ-spidr enhances axon regeneration after peripheral nerve injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797756/ https://www.ncbi.nlm.nih.gov/pubmed/31624232 http://dx.doi.org/10.1038/s41419-019-2027-x |
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