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Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium

Expanded polytetrafluoroethylene (ePTFE) is commonly used in cardiovascular surgery, but usually causes postoperation complications. Although great efforts have been done to relieve these complications or to understand their mechanism, there are no applicable strategies available and no understandin...

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Autores principales: Shan, Yaping, Zhang, Wenbo, Chen, Gang, Shi, Qiqi, Mi, Yaping, Zhang, Huifeng, Jia, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235981/
https://www.ncbi.nlm.nih.gov/pubmed/34239925
http://dx.doi.org/10.1155/2021/5551207
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author Shan, Yaping
Zhang, Wenbo
Chen, Gang
Shi, Qiqi
Mi, Yaping
Zhang, Huifeng
Jia, Bing
author_facet Shan, Yaping
Zhang, Wenbo
Chen, Gang
Shi, Qiqi
Mi, Yaping
Zhang, Huifeng
Jia, Bing
author_sort Shan, Yaping
collection PubMed
description Expanded polytetrafluoroethylene (ePTFE) is commonly used in cardiovascular surgery, but usually causes postoperation complications. Although great efforts have been done to relieve these complications or to understand their mechanism, there are no applicable strategies available and no understanding mechanisms, especially in the myocardium. Here, ePTFE membranes are implanted into the right ventricular outflow tract of rabbits, and the implant-related myocardium is dissected and analyzed by histology and transcriptome sequencing. ePTFE implantation causes myocardium inflammation and fibrosis. There are 1867 differently expressed mRNAs (DEmRNAs, 1107 upregulated and 760 downregulated) and 246 differently expressed lncRNAs (DElncRNAs, 110 upregulated and 136 downregulated) identified. Bioinformatic analysis indicates that the upregulated DEmRNAs and DElncRNAs are mainly involved in inflammatory, immune responses, and extracellular matrix remodeling, while the downregulated DEmRNAs and DElncRNAs are predominantly functioned in the metabolism and cardiac remodeling. Analysis of coexpression and regulatory relationship of DEmRNAs and DElncRNAs reveals that most DElncRNAs are trans-regulated on the relevant DEmRNAs. In conclusion, ePTFE implantation causes severe myocardial tissue damages and alters the transcriptome profiles of the myocardium. Such novel data may provide a landscape of mechanisms underlying the adverse reactions caused by ePTFE implantation and uncover new therapeutic targets for inhibiting the ePTFE-related complications.
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spelling pubmed-82359812021-07-07 Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium Shan, Yaping Zhang, Wenbo Chen, Gang Shi, Qiqi Mi, Yaping Zhang, Huifeng Jia, Bing Biomed Res Int Research Article Expanded polytetrafluoroethylene (ePTFE) is commonly used in cardiovascular surgery, but usually causes postoperation complications. Although great efforts have been done to relieve these complications or to understand their mechanism, there are no applicable strategies available and no understanding mechanisms, especially in the myocardium. Here, ePTFE membranes are implanted into the right ventricular outflow tract of rabbits, and the implant-related myocardium is dissected and analyzed by histology and transcriptome sequencing. ePTFE implantation causes myocardium inflammation and fibrosis. There are 1867 differently expressed mRNAs (DEmRNAs, 1107 upregulated and 760 downregulated) and 246 differently expressed lncRNAs (DElncRNAs, 110 upregulated and 136 downregulated) identified. Bioinformatic analysis indicates that the upregulated DEmRNAs and DElncRNAs are mainly involved in inflammatory, immune responses, and extracellular matrix remodeling, while the downregulated DEmRNAs and DElncRNAs are predominantly functioned in the metabolism and cardiac remodeling. Analysis of coexpression and regulatory relationship of DEmRNAs and DElncRNAs reveals that most DElncRNAs are trans-regulated on the relevant DEmRNAs. In conclusion, ePTFE implantation causes severe myocardial tissue damages and alters the transcriptome profiles of the myocardium. Such novel data may provide a landscape of mechanisms underlying the adverse reactions caused by ePTFE implantation and uncover new therapeutic targets for inhibiting the ePTFE-related complications. Hindawi 2021-06-18 /pmc/articles/PMC8235981/ /pubmed/34239925 http://dx.doi.org/10.1155/2021/5551207 Text en Copyright © 2021 Yaping Shan et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shan, Yaping
Zhang, Wenbo
Chen, Gang
Shi, Qiqi
Mi, Yaping
Zhang, Huifeng
Jia, Bing
Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium
title Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium
title_full Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium
title_fullStr Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium
title_full_unstemmed Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium
title_short Pathological Change and Whole Transcriptome Alternation Caused by ePTFE Implantation in Myocardium
title_sort pathological change and whole transcriptome alternation caused by eptfe implantation in myocardium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235981/
https://www.ncbi.nlm.nih.gov/pubmed/34239925
http://dx.doi.org/10.1155/2021/5551207
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