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Proteomics of the epicardial fat secretome and its role in post-operative atrial fibrillation.

Viviano, A; Yin, X; Zampetaki, A; Fava, M; Gallagher, M; Mayr, M; Jahangiri, M (2018) Proteomics of the epicardial fat secretome and its role in post-operative atrial fibrillation. Europace, 20 (7). pp. 1201-1208. ISSN 1532-2092 https://doi.org/10.1093/europace/eux113
SGUL Authors: Jahangiri, Marjan

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Abstract

Aims: Post-operative atrial fibrillation (POAF) is a predictor of morbidity and mortality after cardiac surgery. Latent predisposing factors may reside in the epicardial adipose tissue (EAT) due to its anatomical position and high protein production rate. In order to explore a possible mechanistic link, we characterized proteins secreted by the EAT preceding the onset of POAF. Methods and results: Epicardial adipose tissue samples were collected from 76 consecutive patients with no history of AF undergoing coronary artery bypass surgery, 50 samples for proteomic analysis and 26 for gene expression studies, further divided according to development of POAF. Ten vs. 10 matched samples representing EAT secretome were analysed by two-dimensional difference in-gel electrophoresis (2D-DIGE) and high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) to identify differentially expressed proteins (P < 0.05, expression change >1.2 fold). Findings were validated by Western blotting on EAT protein extracts and by gene expression studies via quantitative polymerase chain reaction (qPCR). Proteomics returned 35 differentially expressed proteins. Amongst those, gelsolin was down regulated in POAF. Western blot analysis confirmed a significant reduction in gelsolin in the AF group. Gene expression for gelsolin was significantly reduced in the AF group confirming the proteomics findings. Conclusion: For the first time we describe EAT secretome as a possible substrate for POAF. It contains various proteins differentially expressed in patients who later develop POAF. Amongst those gelsolin, involved in inflammation and ion channel regulation, was associated with maintenance of sinus rhythm. Understanding the role of EAT may offer novel insights into prevention and treatment of AF.

Item Type: Article
Additional Information: This is a pre-copyedited, author-produced version of an article accepted for publication in Europace following peer review. The version of record Alessandro Viviano, Xiaoke Yin, Anna Zampetaki, Marika Fava, Mark Gallagher, Manuel Mayr, Marjan Jahangiri, Proteomics of the epicardial fat secretome and its role in post-operative atrial fibrillation, EP Europace, Volume 20, Issue 7, July 2018, Pages 1201–1208 is available online at: https://doi.org/10.1093/europace/eux113
Keywords: Adipose Tissue, Aged, Atrial Fibrillation, Biomarkers, Blotting, Western, Chromatography, High Pressure Liquid, Coronary Artery Bypass, Electrophoresis, Gel, Two-Dimensional, Female, Gelsolin, Gene Expression Regulation, Humans, Male, Middle Aged, Pericardium, Proteomics, Reverse Transcriptase Polymerase Chain Reaction, Risk Factors, Secretory Pathway, Tandem Mass Spectrometry, Treatment Outcome, Pericardium, Adipose Tissue, Humans, Atrial Fibrillation, Gelsolin, Blotting, Western, Treatment Outcome, Coronary Artery Bypass, Chromatography, High Pressure Liquid, Electrophoresis, Gel, Two-Dimensional, Risk Factors, Reverse Transcriptase Polymerase Chain Reaction, Proteomics, Gene Expression Regulation, Aged, Middle Aged, Female, Male, Tandem Mass Spectrometry, Secretory Pathway, Biomarkers, Post-operative atrial fibrillation, Epicardial adipose tissue, Proteomics, Epicardial adipose tissue, Post-operative atrial fibrillation, Proteomics, 1103 Clinical Sciences, Cardiovascular System & Hematology
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Europace
ISSN: 1532-2092
Language: eng
Dates:
DateEvent
1 July 2018Published
5 June 2017Published Online
4 April 2017Accepted
Publisher License: Publisher's own licence
Projects:
Project IDFunderFunder ID
FS/13/18/30207British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
FS/13/2/29892British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
PubMed ID: 28582578
Web of Science ID: WOS:000439059700026
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/109039
Publisher's version: https://doi.org/10.1093/europace/eux113

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