Infiltrating macrophages amplify doxorubicin-induced cardiac damage: role of catecholamines

• Published in: Cellular and molecular life sciences : CMLS 2023-11, Vol.80 (11), p.323-323, Article 323
• Main Authors: Gambardella, Jessica, Santulli, Gaetano, Fiordelisi, Antonella, Cerasuolo, Federica Andrea, Wang, Xujun, Prevete, Nella, Sommella, Eduardo, Avvisato, Roberta, Buonaiuto, Antonietta, Altobelli, Giovanna Giuseppina, Rinaldi, Laura, Chiuso, Francesco, Feliciello, Antonio, Dal Piaz, Fabrizio, Campiglia, Pietro, Ciccarelli, Michele, Morisco, Carmine, Sadoshima, Junichi, Iaccarino, Guido, Sorriento, Daniela
• Format: Article
• Language: English
• Subjects: Apoptosis; Autophagy; Biochemistry; Biomedical and Life Sciences; Biomedicine; Cardiotoxicity; Catecholamines; Cell Biology; Congestive heart failure; Damage prevention; Depletion; Doxorubicin; Flow cytometry; Inflammation; Life Sciences; Macrophages; Myocytes; Original; Original Article
• ISSN: 1420-682X; 1420-9071
• DOI: 10.1007/s00018-023-04922-5

Background The functional contribution of non-myocyte cardiac cells, such as inflammatory cells, in the setup of heart failure in response to doxorubicin (Dox) is recently becoming of growing interest. Objectives The study aims to evaluate the role of macrophages in cardiac damage elicited by Dox treatment. Methods C57BL/6 mice were treated with one intraperitoneal injection of Dox (20 mg/kg) and followed up for 5 days by cardiac ultrasounds (CUS), histological, and flow cytometry evaluations. We also tested the impact of Dox in macrophage-depleted mice. Rat cardiomyoblasts were directly treated with Dox (D-Dox) or with a conditioned medium from cultured murine macrophages treated with Dox (M-Dox). Results In response to Dox, macrophage infiltration preceded cardiac damage. Macrophage depletion prevents Dox-induced damage, suggesting a key role of these cells in promoting cardiotoxicity. To evaluate the crosstalk between macrophages and cardiac cells in response to DOX, we compared the effects of D-Dox and M-Dox in vitro. Cell vitality was lower in cardiomyoblasts and apoptosis was higher in response to M-Dox compared with D-Dox. These events were linked to p53-induced mitochondria morphology, function, and autophagy alterations. We identify a mechanistic role of catecholamines released by Dox-activated macrophages that lead to mitochondrial apoptosis of cardiac cells through β-AR stimulation. Conclusions Our data indicate that crosstalk between macrophages and cardiac cells participates in cardiac damage in response to Dox. Graphical abstract