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Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries

In central nervous system, axons fail to regenerate after injury while in peripheral nervous system, axons retain certain regenerative ability. Dorsal root ganglion (DRG) neuron has an ascending central axon branch and a descending peripheral axon branch stemming from one single axon and serves as a...

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Autores principales: Cao, Hong-Jun, Huang, Li, Zheng, Meng-Ru, Zhang, Tao, Xu, Ling-Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790916/
https://www.ncbi.nlm.nih.gov/pubmed/36578373
http://dx.doi.org/10.3389/fncel.2022.1046050
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author Cao, Hong-Jun
Huang, Li
Zheng, Meng-Ru
Zhang, Tao
Xu, Ling-Chi
author_facet Cao, Hong-Jun
Huang, Li
Zheng, Meng-Ru
Zhang, Tao
Xu, Ling-Chi
author_sort Cao, Hong-Jun
collection PubMed
description In central nervous system, axons fail to regenerate after injury while in peripheral nervous system, axons retain certain regenerative ability. Dorsal root ganglion (DRG) neuron has an ascending central axon branch and a descending peripheral axon branch stemming from one single axon and serves as a suitable model for the comparison of growth competence following central and peripheral axon injuries. Molecular alterations underpin different injury responses of DRG branches have been investigated from many aspects, such as coding gene expression, chromatin accessibility, and histone acetylation. However, changes of circular RNAs are poorly characterized. In the present study, we comprehensively investigate circular RNA expressions in DRGs after rat central and peripheral axon injuries using sequencing analysis and identify a total of 33 differentially expressed circular RNAs after central branch injury as well as 55 differentially expressed circular RNAs after peripheral branch injury. Functional enrichment of host genes of differentially expressed circular RNAs demonstrate the participation of Hippo signaling pathway and Notch signaling pathway after both central and peripheral axon injuries. Circular RNA changes after central axon injury are also linked with apoptosis and cellular junction while changes after peripheral axon injury are associated with metabolism and PTEN-related pathways. Altogether, the present study offers a systematic evaluation of alterations of circular RNAs in rat DRGs following injuries to the central and peripheral axon branches and contributes to the deciphering of essential biological activities and mechanisms behind successful nerve regeneration.
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spelling pubmed-97909162022-12-27 Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries Cao, Hong-Jun Huang, Li Zheng, Meng-Ru Zhang, Tao Xu, Ling-Chi Front Cell Neurosci Neuroscience In central nervous system, axons fail to regenerate after injury while in peripheral nervous system, axons retain certain regenerative ability. Dorsal root ganglion (DRG) neuron has an ascending central axon branch and a descending peripheral axon branch stemming from one single axon and serves as a suitable model for the comparison of growth competence following central and peripheral axon injuries. Molecular alterations underpin different injury responses of DRG branches have been investigated from many aspects, such as coding gene expression, chromatin accessibility, and histone acetylation. However, changes of circular RNAs are poorly characterized. In the present study, we comprehensively investigate circular RNA expressions in DRGs after rat central and peripheral axon injuries using sequencing analysis and identify a total of 33 differentially expressed circular RNAs after central branch injury as well as 55 differentially expressed circular RNAs after peripheral branch injury. Functional enrichment of host genes of differentially expressed circular RNAs demonstrate the participation of Hippo signaling pathway and Notch signaling pathway after both central and peripheral axon injuries. Circular RNA changes after central axon injury are also linked with apoptosis and cellular junction while changes after peripheral axon injury are associated with metabolism and PTEN-related pathways. Altogether, the present study offers a systematic evaluation of alterations of circular RNAs in rat DRGs following injuries to the central and peripheral axon branches and contributes to the deciphering of essential biological activities and mechanisms behind successful nerve regeneration. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9790916/ /pubmed/36578373 http://dx.doi.org/10.3389/fncel.2022.1046050 Text en Copyright © 2022 Cao, Huang, Zheng, Zhang and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Cao, Hong-Jun
Huang, Li
Zheng, Meng-Ru
Zhang, Tao
Xu, Ling-Chi
Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries
title Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries
title_full Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries
title_fullStr Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries
title_full_unstemmed Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries
title_short Characterization of circular RNAs in dorsal root ganglia after central and peripheral axon injuries
title_sort characterization of circular rnas in dorsal root ganglia after central and peripheral axon injuries
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790916/
https://www.ncbi.nlm.nih.gov/pubmed/36578373
http://dx.doi.org/10.3389/fncel.2022.1046050
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