Let-7f: A New Potential Circulating Biomarker Identified by miRNA Profiling of Cells Isolated from Human Abdominal Aortic Aneurysm

• Main Authors: Rafaelle Spear, Ludovic Boytard, Renaud Blervaque, Maggy Chwastyniak, David Hot, Jonathan Vanhoutte, Nicolas Lamblin, Philippe Amouyel, Florence Pinet
• Format: Article
• Language: English
• Published: MDPI AG 2019-11-01
• Series: International Journal of Molecular Sciences
• Subjects: abdominal aortic aneurysm; microrna; macrophages; smooth muscle cells
• Online Access: https://www.mdpi.com/1422-0067/20/21/5499

Abdominal aortic aneurysm (AAA) is a progressive vascular disease responsible for 1&#8722;4% of the deaths in elderly men. This study aimed to characterize specific microRNA (miRNA) expression in aneurysmal smooth muscle cells (SMCs) and macrophages in order to identify circulating miRNAs associated with AAA. We screened 850 miRNAs in aneurysmal SMCs, M1 and M2 macrophages, and in control SMCs isolated by micro-dissection from aortic biopsies using microarray analysis. In all, 92 miRNAs were detected and 10 miRNAs were selected for validation by qRT-PCR in isolated cells (<i>n</i> = 5), whole control and aneurysmal aorta biopsies (<i>n</i> = 13), and plasma from patients (<i>n</i> = 24) undergoing AAA (over 50 mm) repair matched to patients (<i>n</i> = 18) with peripheral arterial disease (PAD) with atherosclerosis but not AAA. Seven miRNAs were modulated similarly in all aneurysmal cells. The Let-7f was downregulated in aneurysmal cells compared to control SMCs with a significant lower expression in M1 compared to M2 macrophages (0.1 fold, <i>p</i> = 0.03), correlated with a significant downregulation in whole aneurysmal aorta compared to control aorta (0.2 fold, <i>p</i> = 0.03). Significant levels of circulating let-7f (<i>p</i> = 0.048) were found in AAA patients compared to PAD patients with no significant correlation with aortic diameter (<i>R</i>² = 0.03). Our study underlines the utility of profiling isolated aneurysmal cells to identify other miRNAs for which the modulation of expression might be masked when the whole aorta is used. The results highlight let-7f as a new potential biomarker for AAA.