Association of Cardiac Galectin-3 Expression, Myocarditis, and Fibrosis in Chronic Chagas Disease Cardiomyopathy

• DOI: 10.1016/j.ajpath.2017.01.016
• Publication Date: 2017-03-17T06:00:25Z
• Authors: Bruno Solano de F...; Daniela Nasciment...; Rejane Hughes Car...; Gabriela Louise d...; Bruno Diaz Paredes; Luciana Aragão Fr...; Carine Machado Az...; Juliana Fraga Vas...; Cassio Santana Meira; Paulo Chenaud Neto; Simone Garcia Mac...; Kátia Nunes da Silva; Kyan James Allahdadi; Fabio Tavora; João David de Sou...; Ricardo Ribeiro d...; Milena Botelho Pe...
• Keywords: Chagas Disease; Pathogenesis; Cardiac Fibrosis; Galectin-3; Proinflammatory cytokine

Chronic Chagas disease cardiomyopathy, caused by Trypanosoma cruzi infection, is a major cause of heart failure in Latin America. Galectin-3 (Gal-3) has been linked to cardiac remodeling and poor prognosis in heart failure of different etiologies. Herein, we investigated the involvement of Gal-3 in the disease pathogenesis and its role as a target for disease intervention. Gal-3 expression in mouse hearts was evaluated during T. cruzi infection by confocal microscopy and flow cytometry analysis, showing a high expression in macrophages, T cells, and fibroblasts. In vitro studies using Gal-3 knockdown in cardiac fibroblasts demonstrated that Gal-3 regulates cell survival, proliferation, and type I collagen synthesis. In vivo blockade of Gal-3 with N-acetyl-d-lactosamine in T. cruzi-infected mice led to a significant reduction of cardiac fibrosis and inflammation in the heart. Moreover, a modulation in the expression of proinflammatory genes in the heart was observed. Finally, histological analysis in human heart samples obtained from subjects with Chagas disease who underwent heart transplantation showed the expression of Gal-3 in areas of inflammation, similar to the mouse model. Our results indicate that Gal-3 plays a role in the pathogenesis of experimental chronic Chagas disease, favoring inflammation and fibrogenesis. Moreover, by demonstrating Gal-3 expression in human hearts, our finding reinforces that this protein could be a novel target for drug development for Chagas cardiomyopathy.