Epicardial and endothelial cell activation concurs with extracellular matrix remodeling in atrial fibrillation. Issue 11 (4th November 2021)

• Record Type: Journal Article
• Authors: van den Berg, Nicoline W. E.; Kawasaki, Makiri; Fabrizi, Benedetta; Nariswari, Fransisca A.; Verduijn, Arianne C.; Neefs, Jolien; Wesselink, Robin; Al‐Shama, Rushd F. M.; van der Wal, Allard C.; de Boer, Onno J.; Aten, Jan; Driessen, Antoine H. G.; Jongejan, Aldo; de Groot, Joris R.
• Is Part Of: Clinical and translational medicine. Volume 11:Issue 11(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-11-04
• Subjects: angiogenesis -- arrhythmias -- atrial fibrillation -- atrial remodeling -- epithelial‐to‐mesenchymal transition -- extracellular matrix -- transcriptome; Clinical medicine -- Periodicals; Medicine, Experimental -- Periodicals; Medical innovations -- Periodicals; Molecular biology -- Periodicals; Pathology, Molecular -- Periodicals; 616.027
• DOI: 10.1002/ctm2.558
• Languages: English
• ISSNs: 2001-1326

Abstract

Abstract: Background: Improved understanding of the interconnectedness of structural remodeling processes in atrial fibrillation (AF) in patients could identify targets for future therapies. Methods: We present transcriptome sequencing of atrial tissues of patients without AF, with paroxysmal AF, and persistent AF (total n = 64). RNA expression levels were validated in the same and an independent cohort with qPCR. Biological processes were assessed with histological and immunohistochemical analyses. Results: In AF patients, epicardial cell gene expression decreased, contrasting with an upregulation of epithelial‐to‐mesenchymal transition (EMT) and mesenchymal cell gene expression. Immunohistochemistry demonstrated thickening of the epicardium and an increased proportion of (myo)fibroblast‐like cells in the myocardium, supporting enhanced EMT in AF. We furthermore report an upregulation of endothelial cell proliferation, angiogenesis, and endothelial signaling. EMT and endothelial cell proliferation concurred with increased interstitial (myo)fibroblast‐like cells and extracellular matrix gene expression including enhanced tenascin‐C, thrombospondins, biglycan, and versican. Morphological analyses discovered increased and redistributed glycosaminoglycans and collagens in the atria of AF patients. Signaling pathways, including cell–matrix interactions, PI3K‐AKT, and Notch signaling that could regulate mesenchymal cell activation, were upregulated. Conclusion: Our results suggest that EMT and endothelial cell proliferation work in concert and characterize the (myo)fibroblast recruitment and ECM remodeling of AF. These processes could guide future research toward the discovery of targets for AF therapy. Abstract : Various signaling pathways are upregulated in atrial fibrillation, which can activate epithelial‐to‐mesenchymal transition and endothelial cell proliferation and differentiation. These processes are associated with increased interstitial fibroblasts and increased and altered extracellular matrix deposits including glycoproteins and glycosaminoglycans. EC, endothelial cell; ECM, extracellular matrix; EMT, epithelial‐to‐mesenchymal transition; FB, fibroblast; MSC, mesenchymal cells; PVC, perivascular cell.