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Identification of atrial fibrillation‐associated lncRNAs in atria from patients with rheumatic mitral valve disease
Author(s) -
Wu Jine,
Han Dan,
Shi Rui,
Chen Mingxia,
Sun Jingwen,
Tian Hongyan,
Yan Yang
Publication year - 2019
Publication title -
microscopy research and technique
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 118
eISSN - 1097-0029
pISSN - 1059-910X
DOI - 10.1002/jemt.23261
Subject(s) - atrial fibrillation , kegg , masson's trichrome stain , blot , sinus rhythm , medicine , pathogenesis , gene expression , fibrosis , western blot , pathology , mitral valve , gene , cardiology , biology , transcriptome , genetics
Objective We analysed lncRNA expression profiles in atrial samples from patients with rheumatic mitral valve disease (RMVD) to identify the potential differences in atrial fibrillation (AF)‐associated lncRNAs between RMVD patients with AF and sinus rhythm (SR). Methods Masson's trichrome staining and scanning electron microscopy were performed to evaluate the tissue morphology. Western blotting was performed to detect the expression of fibrosis‐related proteins. Difference analysis, Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) and gene co‐expression networks were also adopted to perform IncRNA expression profile analysis in atrial samples. Results Masson's trichrome staining indicated higher contents of fat deposition and fibrous tissue in atrial samples from patients with AF than from patients with SR. Western blotting showed that fibrosis‐related proteins, including smad2, TGFβ1, MMP9, and TIMP1, were upregulated in atrial samples from patients with AF compared to those from patients with SR. lncRNA expression profiles showed different lncRNA expression levels between RMVD patients with AF and SR. Moreover, GO, KEGG and gene co‐expression networks showed consistent results and indicated that differentially expressed genes might contribute to the pathogenesis of AF. Conclusion Our results revealed the potential roles of IncRNAs in the development of AF in patients with RMVD, and lncRNAs may be responsible for morphological and physiological differences in atria between RMVD patients with AF and SR.