Identification of atrial fibrillation-associated lncRNAs in atria from patients with rheumatic mitral valve disease.
Atrial Fibrillation
/ etiology
Humans
Microscopy, Electron, Scanning
Mitral Valve
/ pathology
RNA, Long Noncoding
/ genetics
RNA, Messenger
/ genetics
Rheumatic Heart Disease
/ genetics
Smad2 Protein
/ genetics
Tissue Inhibitor of Metalloproteinase-1
/ genetics
Transforming Growth Factor beta1
/ genetics
Up-Regulation
atrial fibrillation
fibrosis
gene expression profile
long noncoding RNA
rheumatic mitral valve disease
Journal
Microscopy research and technique
ISSN: 1097-0029
Titre abrégé: Microsc Res Tech
Pays: United States
ID NLM: 9203012
Informations de publication
Date de publication:
Jul 2019
Jul 2019
Historique:
received:
27
08
2018
revised:
23
01
2019
accepted:
02
03
2019
pubmed:
12
4
2019
medline:
13
11
2019
entrez:
12
4
2019
Statut:
ppublish
Résumé
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). 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. 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. 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.
Substances chimiques
RNA, Long Noncoding
0
RNA, Messenger
0
SMAD2 protein, human
0
Smad2 Protein
0
TGFB1 protein, human
0
TIMP1 protein, human
0
Tissue Inhibitor of Metalloproteinase-1
0
Transforming Growth Factor beta1
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1136-1144Subventions
Organisme : Scientific and Technological projects in Shaanxi Province
ID : 2014K11-03-01-03
Organisme : The Clinical Research Award of the First Affiliated Hospital of Xi'an Jiaotong University
ID : XJTU1AF-CRF-2015-007
Organisme : First Affiliated Hospital of Xi'an Jiaotong University
ID : XJTU1AF-CRF-2015-007
Informations de copyright
© 2019 Wiley Periodicals, Inc.