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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...

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Autores principales: Mao, Susu, Huang, Tao, Chen, Yuanyuan, Shen, Longxiang, Zhou, Shuoshuo, Zhang, Shanshan, Yu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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