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Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury

In our previous study, we investigated the dynamic expression of cytokines in the distal nerve stumps after peripheral nerve injury using microarray analysis, which can characterize the dynamic expression of proteins. In the present study, we used a rat model of right sciatic nerve transection to ex...

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Autores principales: Cheng, Xiao-Qing, Xu, Wen-Jing, Ding, Xiao, Han, Gong-Hai, Wei, Shuai, Liu, Ping, Meng, Hao-Ye, Shang, Ai-Jia, Wang, Yu, Wang, Ai-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178785/
https://www.ncbi.nlm.nih.gov/pubmed/33229723
http://dx.doi.org/10.4103/1673-5374.295348
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author Cheng, Xiao-Qing
Xu, Wen-Jing
Ding, Xiao
Han, Gong-Hai
Wei, Shuai
Liu, Ping
Meng, Hao-Ye
Shang, Ai-Jia
Wang, Yu
Wang, Ai-Yuan
author_facet Cheng, Xiao-Qing
Xu, Wen-Jing
Ding, Xiao
Han, Gong-Hai
Wei, Shuai
Liu, Ping
Meng, Hao-Ye
Shang, Ai-Jia
Wang, Yu
Wang, Ai-Yuan
author_sort Cheng, Xiao-Qing
collection PubMed
description In our previous study, we investigated the dynamic expression of cytokines in the distal nerve stumps after peripheral nerve injury using microarray analysis, which can characterize the dynamic expression of proteins. In the present study, we used a rat model of right sciatic nerve transection to examine changes in the expression of cytokines at 1, 7, 14 and 28 days after injury using protein microarray analysis. Interleukins were increased in the distal nerve stumps at 1–14 days post nerve transection. However, growth factors and growth factor-related proteins were mainly upregulated in the proximal nerve stumps. The P-values of the inflammatory response, apoptotic response and cell-cell adhesion in the distal stumps were higher than those in the proximal nerve stumps, but the opposite was observed for angiogenesis. The number of cytokines related to axons in the distal stumps was greater than that in the proximal stumps, while the percentage of cytokines related to axons in the distal stumps was lower than that in the proximal nerve stumps. Visualization of the results revealed the specific expression patterns and differences in cytokines in and between the proximal and distal nerve stumps. Our findings offer potential therapeutic targets and should help advance the development of clinical treatments for peripheral nerve injury. Approval for animal use in this study was obtained from the Animal Ethics Committee of the Chinese PLA General Hospital on September 7, 2016 (approval No. 2016-x9-07).
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spelling pubmed-81787852021-06-22 Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury Cheng, Xiao-Qing Xu, Wen-Jing Ding, Xiao Han, Gong-Hai Wei, Shuai Liu, Ping Meng, Hao-Ye Shang, Ai-Jia Wang, Yu Wang, Ai-Yuan Neural Regen Res Research Article In our previous study, we investigated the dynamic expression of cytokines in the distal nerve stumps after peripheral nerve injury using microarray analysis, which can characterize the dynamic expression of proteins. In the present study, we used a rat model of right sciatic nerve transection to examine changes in the expression of cytokines at 1, 7, 14 and 28 days after injury using protein microarray analysis. Interleukins were increased in the distal nerve stumps at 1–14 days post nerve transection. However, growth factors and growth factor-related proteins were mainly upregulated in the proximal nerve stumps. The P-values of the inflammatory response, apoptotic response and cell-cell adhesion in the distal stumps were higher than those in the proximal nerve stumps, but the opposite was observed for angiogenesis. The number of cytokines related to axons in the distal stumps was greater than that in the proximal stumps, while the percentage of cytokines related to axons in the distal stumps was lower than that in the proximal nerve stumps. Visualization of the results revealed the specific expression patterns and differences in cytokines in and between the proximal and distal nerve stumps. Our findings offer potential therapeutic targets and should help advance the development of clinical treatments for peripheral nerve injury. Approval for animal use in this study was obtained from the Animal Ethics Committee of the Chinese PLA General Hospital on September 7, 2016 (approval No. 2016-x9-07). Wolters Kluwer - Medknow 2020-11-16 /pmc/articles/PMC8178785/ /pubmed/33229723 http://dx.doi.org/10.4103/1673-5374.295348 Text en Copyright: © 2021 Neural Regeneration Research https://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
Cheng, Xiao-Qing
Xu, Wen-Jing
Ding, Xiao
Han, Gong-Hai
Wei, Shuai
Liu, Ping
Meng, Hao-Ye
Shang, Ai-Jia
Wang, Yu
Wang, Ai-Yuan
Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury
title Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury
title_full Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury
title_fullStr Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury
title_full_unstemmed Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury
title_short Bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury
title_sort bioinformatic analysis of cytokine expression in the proximal and distal nerve stumps after peripheral nerve injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178785/
https://www.ncbi.nlm.nih.gov/pubmed/33229723
http://dx.doi.org/10.4103/1673-5374.295348
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