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Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury
The peripheral nervous system has the potential to regenerate after nerve injury owing to the intrinsic regrowth ability of neurons and the permissive microenvironment. The regenerative process involves numerous gene expression changes, in which transcription factors play a critical role. Previously...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126133/ https://www.ncbi.nlm.nih.gov/pubmed/30127124 http://dx.doi.org/10.4103/1673-5374.237183 |
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author | Qin, Jing Wu, Jian-Cheng Wang, Qi-Hui Zhou, Song-Lin Mao, Su-Su Yao, Chun |
author_facet | Qin, Jing Wu, Jian-Cheng Wang, Qi-Hui Zhou, Song-Lin Mao, Su-Su Yao, Chun |
author_sort | Qin, Jing |
collection | PubMed |
description | The peripheral nervous system has the potential to regenerate after nerve injury owing to the intrinsic regrowth ability of neurons and the permissive microenvironment. The regenerative process involves numerous gene expression changes, in which transcription factors play a critical role. Previously, we profiled dysregulated genes in dorsal root ganglion neurons at different time points (0, 3 and 9 hours, and 1, 4 and 7 days) after sciatic nerve injury in rats by RNA sequencing. In the present study, we investigated differentially expressed transcription factors following nerve injury, and we identified enriched molecular and cellular functions of these transcription factors by Ingenuity Pathway Analysis. This analysis revealed the dynamic changes in the expression of transcription factors involved in cell death at different time points following sciatic nerve injury. In addition, we constructed regulatory networks of the differentially expressed transcription factors in cell death and identified some key transcription factors (such as STAT1, JUN, MYC and IRF7). We confirmed the changes in expression of some key transcription factors (STAT1 and IRF7) by quantitative reverse transcription-polymerase chain reaction. Collectively, our analyses provide a global overview of transcription factor changes in dorsal root ganglia after sciatic nerve injury and offer insight into the regulatory transcription factor networks involved in cell death. |
format | Online Article Text |
id | pubmed-6126133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61261332018-09-12 Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury Qin, Jing Wu, Jian-Cheng Wang, Qi-Hui Zhou, Song-Lin Mao, Su-Su Yao, Chun Neural Regen Res Research Article The peripheral nervous system has the potential to regenerate after nerve injury owing to the intrinsic regrowth ability of neurons and the permissive microenvironment. The regenerative process involves numerous gene expression changes, in which transcription factors play a critical role. Previously, we profiled dysregulated genes in dorsal root ganglion neurons at different time points (0, 3 and 9 hours, and 1, 4 and 7 days) after sciatic nerve injury in rats by RNA sequencing. In the present study, we investigated differentially expressed transcription factors following nerve injury, and we identified enriched molecular and cellular functions of these transcription factors by Ingenuity Pathway Analysis. This analysis revealed the dynamic changes in the expression of transcription factors involved in cell death at different time points following sciatic nerve injury. In addition, we constructed regulatory networks of the differentially expressed transcription factors in cell death and identified some key transcription factors (such as STAT1, JUN, MYC and IRF7). We confirmed the changes in expression of some key transcription factors (STAT1 and IRF7) by quantitative reverse transcription-polymerase chain reaction. Collectively, our analyses provide a global overview of transcription factor changes in dorsal root ganglia after sciatic nerve injury and offer insight into the regulatory transcription factor networks involved in cell death. Medknow Publications & Media Pvt Ltd 2018-09 /pmc/articles/PMC6126133/ /pubmed/30127124 http://dx.doi.org/10.4103/1673-5374.237183 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 Qin, Jing Wu, Jian-Cheng Wang, Qi-Hui Zhou, Song-Lin Mao, Su-Su Yao, Chun Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury |
title | Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury |
title_full | Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury |
title_fullStr | Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury |
title_full_unstemmed | Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury |
title_short | Transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury |
title_sort | transcription factor networks involved in cell death in the dorsal root ganglia following peripheral nerve injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126133/ https://www.ncbi.nlm.nih.gov/pubmed/30127124 http://dx.doi.org/10.4103/1673-5374.237183 |
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