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Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury

Long noncoding RNAs (lncRNAs) participate in a variety of biological processes and diseases. However, the expression and function of lncRNAs after spinal cord injury has not been extensively analyzed. In this study of right side hemisection of the spinal cord at T10, we detected the expression of ln...

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Autores principales: Liu, Wei, Tao, Jin-Cheng, Zhu, Sheng-Ze, Dai, Chao-Lun, Wang, Ya-Xian, Yu, Bin, Yao, Chun, Sun, Yu-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083175/
https://www.ncbi.nlm.nih.gov/pubmed/35259853
http://dx.doi.org/10.4103/1673-5374.337052
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author Liu, Wei
Tao, Jin-Cheng
Zhu, Sheng-Ze
Dai, Chao-Lun
Wang, Ya-Xian
Yu, Bin
Yao, Chun
Sun, Yu-Yu
author_facet Liu, Wei
Tao, Jin-Cheng
Zhu, Sheng-Ze
Dai, Chao-Lun
Wang, Ya-Xian
Yu, Bin
Yao, Chun
Sun, Yu-Yu
author_sort Liu, Wei
collection PubMed
description Long noncoding RNAs (lncRNAs) participate in a variety of biological processes and diseases. However, the expression and function of lncRNAs after spinal cord injury has not been extensively analyzed. In this study of right side hemisection of the spinal cord at T10, we detected the expression of lncRNAs in the proximal tissue of T10 lamina at different time points and found 445 lncRNAs and 6522 mRNA were differentially expressed. We divided the differentially expressed lncRNAs into 26 expression trends and analyzed Profile 25 and Profile 2, the two expression trends with the most significant difference. Our results showed that the expression of 68 lncRNAs in Profile 25 rose first and remained high 3 days post-injury. There were 387 mRNAs co-expressed with the 68 lncRNAs in Profile 25. The co-expression network showed that the co-expressed genes were mainly enriched in cell division, inflammatory response, FcγR-mediated cell phagocytosis signaling pathway, cell cycle and apoptosis. The expression of 56 lncRNAs in Profile2 first declined and remained low after 3 days post-injury. There were 387 mRNAs co-expressed with the 56 lncRNAs in Profile 2. The co-expression network showed that the co-expressed genes were mainly enriched in the chemical synaptic transmission process and in the signaling pathway of neuroactive ligand-receptor interaction. The results provided the expression and regulatory network of the main lncRNAs after spinal cord injury and clarified their co-expressed gene enriched biological processes and signaling pathways. These findings provide a new direction for the clinical treatment of spinal cord injury.
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spelling pubmed-90831752022-05-10 Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury Liu, Wei Tao, Jin-Cheng Zhu, Sheng-Ze Dai, Chao-Lun Wang, Ya-Xian Yu, Bin Yao, Chun Sun, Yu-Yu Neural Regen Res Research Article Long noncoding RNAs (lncRNAs) participate in a variety of biological processes and diseases. However, the expression and function of lncRNAs after spinal cord injury has not been extensively analyzed. In this study of right side hemisection of the spinal cord at T10, we detected the expression of lncRNAs in the proximal tissue of T10 lamina at different time points and found 445 lncRNAs and 6522 mRNA were differentially expressed. We divided the differentially expressed lncRNAs into 26 expression trends and analyzed Profile 25 and Profile 2, the two expression trends with the most significant difference. Our results showed that the expression of 68 lncRNAs in Profile 25 rose first and remained high 3 days post-injury. There were 387 mRNAs co-expressed with the 68 lncRNAs in Profile 25. The co-expression network showed that the co-expressed genes were mainly enriched in cell division, inflammatory response, FcγR-mediated cell phagocytosis signaling pathway, cell cycle and apoptosis. The expression of 56 lncRNAs in Profile2 first declined and remained low after 3 days post-injury. There were 387 mRNAs co-expressed with the 56 lncRNAs in Profile 2. The co-expression network showed that the co-expressed genes were mainly enriched in the chemical synaptic transmission process and in the signaling pathway of neuroactive ligand-receptor interaction. The results provided the expression and regulatory network of the main lncRNAs after spinal cord injury and clarified their co-expressed gene enriched biological processes and signaling pathways. These findings provide a new direction for the clinical treatment of spinal cord injury. Wolters Kluwer - Medknow 2022-02-28 /pmc/articles/PMC9083175/ /pubmed/35259853 http://dx.doi.org/10.4103/1673-5374.337052 Text en Copyright: © 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
Liu, Wei
Tao, Jin-Cheng
Zhu, Sheng-Ze
Dai, Chao-Lun
Wang, Ya-Xian
Yu, Bin
Yao, Chun
Sun, Yu-Yu
Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury
title Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury
title_full Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury
title_fullStr Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury
title_full_unstemmed Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury
title_short Expression and regulatory network of long noncoding RNA in rats after spinal cord hemisection injury
title_sort expression and regulatory network of long noncoding rna in rats after spinal cord hemisection injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083175/
https://www.ncbi.nlm.nih.gov/pubmed/35259853
http://dx.doi.org/10.4103/1673-5374.337052
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