The effects of inflammation on connexin 43 in chronic Chagas disease cardiomyopathy

被引:1
|
作者
Barreto, Breno Cardim [1 ,2 ,3 ]
das Neves, Maria Vitoria Gomes [1 ,2 ]
Cardoso, Carine Machado Azevedo [1 ]
Meira, Cassio Santana [1 ,3 ]
Daltro, Pamela Santana [2 ]
Figueira, Claudio Pereira [1 ]
Santos, Girlaine Cafe [1 ,2 ]
Silva, Daniela Nascimento [3 ]
Tavora, Fabio [4 ]
de Souza Neto, Joao David [4 ]
Macambira, Simone Garcia [1 ,2 ]
Lampe, Paul D. [5 ]
Coutinho, Keyla Cristiny da Silva [6 ]
Brunswick, Tais Hanae Kasai [6 ]
dos Santos, Ricardo Ribeiro [1 ,3 ]
de Carvalho, Antonio Carlos Campos [6 ]
Soares, Milena Botelho Pereira [1 ,3 ]
机构
[1] Oswaldo Cruz Fdn IGM FIOCRUZ BA, Goncalo Moniz Inst, Salvador, Brazil
[2] Fed Univ Bahia UFBA, Dept Biochem & Biophys, Salvador, BA, Brazil
[3] Univ Ctr SENAI CIMATEC, SENAI Inst Innovat Hlth Adv Syst CIMATEC ISI SAS, Salvador, BA, Brazil
[4] Messejana Heart & Lung Hosp, Fortaleza, Ceara, Brazil
[5] Fred Hutchinson Canc Ctr, Translat Res Program, Seattle, WA USA
[6] Univ Fed Rio de Janeiro, Biophys Inst Carlos Chagas Filho, Rio De Janeiro, Brazil
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
Chagas disease; cardiomyopathy; connexin; 43; arrhythmias; inflammation; GAP-JUNCTION; PHOSPHORYLATION; HEART; ARRHYTHMIAS; MECHANISMS; EXPRESSION; TERMINUS;
D O I
10.3389/fimmu.2024.1440662
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Cardiac arrhythmias are the main cause of sudden death due to Chronic Chagasic Cardiomyopathy (CCC). Here we investigated alterations in connexin 43 (Cx43) expression and phosphorylation in cardiomyocytes as well as associations with cardiac arrhythmias in CCC.Methods C57Bl/6 mice infected with Trypanosoma cruzi underwent cardiac evaluations at 6 and 12 months after infection via treadmill testing and EKG. Histopathology, cytokine gene expression, and distribution of total Cx43 and its phosphorylated forms Cx43S368 and Cx43S325/328/330 were investigated. Human heart samples obtained from subjects with CCC were submitted to immunofluorescence analysis. In vitro simulation of a pro-inflammatory microenvironment (IL-1 beta, TNF, and IFN-gamma) was performed in H9c2 cells and iPSC-derived cardiomyocytes to evaluate Cx43 distribution, action potential duration, and Lucifer Yellow dye transfer.Results Mice chronically infected with T. cruzi exhibited impaired cardiac function associated with increased inflammation, fibrosis and upregulated IL-1 beta, TNF, and IFN-gamma gene expression. Confocal microscopy revealed altered total Cx43, Cx43S368 and Cx43S325/328/330 localization and phosphorylation patterns in CCC, with dispersed staining outside the intercalated disc areas, i.e., in lateral membranes and the cytoplasm. Reduced co-localization of total Cx43 and N-cadherin was observed in the intercalated discs of CCC mouse hearts compared to controls. Similar results were obtained in human CCC heart samples, which showed Cx43 distribution outside the intercalated discs. Stimulation of human iPSC-derived cardiomyocytes or H9c2 cells with IL-1 beta, TNF, and IFN-gamma induced alterations in Cx43 localization, reduced action potential duration and dye transfer between adjacent cells.Conclusion Heart inflammation in CCC affects the distribution and phosphorylation pattern of Cx43, which may contribute to the generation of conduction disturbances in Chagas disease.
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页数:16
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