Developmental endothelial locus-1 protects from hypertension-induced cardiovascular remodeling via immunomodulation
Theresa Failer, … , Vladimir Todorov, Irakli Kopaliani
Theresa Failer, … , Vladimir Todorov, Irakli Kopaliani
Published February 8, 2022
Citation Information: J Clin Invest. 2022;132(6):e126155. https://doi.org/10.1172/JCI126155.
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Research Article Cardiology Inflammation

Developmental endothelial locus-1 protects from hypertension-induced cardiovascular remodeling via immunomodulation

Abstract

The causative role of inflammation in hypertension-related cardiovascular diseases is evident and calls for development of specific immunomodulatory therapies. We tested the therapeutic efficacy and mechanisms of action of developmental endothelial locus-1 (DEL-1), an endogenous antiinflammatory factor, in angiotensin II– (ANGII–) and deoxycorticosterone acetate–salt–induced (DOCA-salt–induced) cardiovascular organ damage and hypertension. By using mice with endothelial overexpression of DEL-1 (EC-Del1 mice) and performing preventive and interventional studies by injecting recombinant DEL-1 in mice, we showed that DEL-1 improved endothelial function and abrogated aortic adventitial fibrosis, medial thickening, and loss of elastin. DEL-1 also protected the mice from cardiac concentric hypertrophy and interstitial and perivascular coronary fibrosis and improved left ventricular function and myocardial coronary perfusion. DEL-1 prevented aortic stiffness and abolished the progression of hypertension. Mechanistically, DEL-1 acted by inhibiting αvβ3 integrin–dependent activation of pro-MMP2 in mice and in human isolated aorta. Moreover, DEL-1 stabilized αvβ3 integrin–dependent CD25+FoxP3+ Treg numbers and IL-10 levels, which were associated with decreased recruitment of inflammatory cells and reduced production of proinflammatory cytokines in cardiovascular organs. The demonstrated effects and immune-modulating mechanisms of DEL-1 in abrogation of cardiovascular remodeling and progression of hypertension identify DEL-1 as a potential therapeutic factor.

Authors

Theresa Failer, Michael Amponsah-Offeh, Aleš Neuwirth, Ioannis Kourtzelis, Pallavi Subramanian, Peter Mirtschink, Mirko Peitzsch, Klaus Matschke, Sems M. Tugtekin, Tetsuhiro Kajikawa, Xiaofei Li, Anne Steglich, Florian Gembardt, Annika C. Wegner, Christian Hugo, George Hajishengallis, Triantafyllos Chavakis, Andreas Deussen, Vladimir Todorov, Irakli Kopaliani

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Figure 1

EC-Del1 mice are protected from ANGII-induced cardiovascular remodeling.

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EC-Del1 mice are protected from ANGII-induced cardiovascular remodeling....
1.5 mg/kg/d ANGII or vehicle was infused in EC-Del1 and WT littermates for 4 weeks. Histological stainings and analysis of aortic adventitial collagen (A and D), medial wall thickness (B and E), and medial elastin (C and F) on the 28th day of ANGII or vehicle infusion. Histological stainings and analysis of cardiac lumen-to-wall ratio (G and K), cardiomyocyte cross-sectional area (H and L), interstitial (I and M) and perivascular coronary (J and N) collagen (n = 6–10 mice per group). Data are represented as mean ± SEM. *P < 0.05; **P < 0.01, 2-way ANOVA with Bonferroni’s post hoc test to adjust for multiple comparisons.