Analysis of local extracellular matrix identifies different aetiologies behind bicuspid and tricuspid aortic valve degeneration and suggests therapies

• DOI: 10.1007/s00018-023-04926-1
• Publication Date: 2023-08-26T15:02:10Z
• Authors: Christian M. Beusch; Oscar E. Simonson; Johan O. Wedin; Pierre Sabatier; Ulrika Felldin; Sandeep Kadekar; Cecilia Österholm; Ákos Végvári; Roman A. Zubarev; Karin Fromell; Bo Nilson; Stefan James; Elisabeth Ståhle; Karl-Henrik Grinnemo; Sergey Rodin
• Keywords: Proteomics; Kardiologi; Cell- och molekylärbiologi; Tenascin; Extracellular matrix; Aortic stenosis/regurgitation; Extracellular Matrix; Kardiologi och kardiovaskulära sjukdomar; Aortic Valve; Humans; Cardiac and Cardiovascular Systems; Original Article; Cardiology and Cardiovascular Disease; Cell and Molecular Biology; Aorta

AbstractAortic valve degeneration (AVD) is a life-threatening condition that has no medical treatment and lacks individual therapies. Although extensively studied with standard approaches, aetiologies behind AVD are unclear. We compared abundances of extracellular matrix (ECM) proteins from excised valve tissues of 88 patients with isolated AVD of normal tricuspid (TAV) and congenital bicuspid aortic valves (BAV), quantified more than 1400 proteins per ECM sample by mass spectrometry, and demonstrated that local ECM preserves molecular cues of the pathophysiological processes. The BAV ECM showed enrichment with fibrosis markers, namely Tenascin C, Osteoprotegerin, and Thrombospondin-2. The abnormal physical stress on BAV may cause a mechanical injury leading to a continuous Tenascin C-driven presence of myofibroblasts and persistent fibrosis. The TAV ECM exhibited enrichment with Annexin A3 (p = 1.1 × 10–16 and the fold change 6.5) and a significant deficit in proteins involved in high-density lipid metabolism. These results were validated by orthogonal methods. The difference in the ECM landscape suggests distinct aetiologies between AVD of BAV and TAV; warrants different treatments of the patients with BAV and TAV; elucidates the molecular basis of AVD; and implies possible new therapeutic approaches. Our publicly available database (human_avd_ecm.surgsci.uu.se) is a rich source for medical doctors and researchers who are interested in AVD or heart ECM in general. Systematic proteomic analysis of local ECM using the methods described here may facilitate future studies of various tissues and organs in development and disease.