Identification of atrial fibrillation-associated lncRNAs in atria from patients with 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
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.

Identifiants

pubmed: 30974026
doi: 10.1002/jemt.23261
doi:

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

1136-1144

Subventions

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.

Auteurs

Jine Wu (J)

Department of Cardiovascular Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Department of Cardiovascular Medicine, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Dan Han (D)

Department of Cardiovascular Medicine, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Rui Shi (R)

Department of Cardiovascular Medicine, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Mingxia Chen (M)

Medical Department of Xi'an Jiaotong University, Electron Microscope Room, Xi'an, China.

Jingwen Sun (J)

Department of Cardiovascular Medicine, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Hongyan Tian (H)

Department of Peripheral Vascular Disease, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Yang Yan (Y)

Department of Cardiovascular Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

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Classifications MeSH