Gene Expression Changes Associated with Myocarditis and Fibrosis in Hearts of Mice with Chronic Chagasic Cardiomyopathy

被引:54
作者
Pereira Soares, Milena Botelho [1 ,2 ]
de Lima, Ricardo Santana [1 ]
Rocha, Leonardo Lima [1 ]
Vasconcelos, Juliana Fraga [1 ]
Rogatto, Silvia Regina [3 ,4 ]
dos Santos, Ricardo Ribeiro [1 ,2 ]
Iacobas, Sanda [7 ]
Goldenberg, Regina Coeli [5 ]
Iacobas, Dumitru Andrei [7 ]
Tanowitz, Herbert Bernard [8 ,9 ]
Campos de Carvalho, Antonio Carlos [5 ,6 ]
Spray, David Conover [8 ]
机构
[1] Fundacao Oswaldo Cruz, Ctr Pesquisas Goncalo Moniz, Salvador, BA, Brazil
[2] Hosp Sao Rafael, Salvador, BA, Brazil
[3] Univ Estado Sao Paulo, Fac Med, Dept Urol, Botucatu, SP, Brazil
[4] Hosp Canc AC Camargo, Sao Paulo, Brazil
[5] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, BR-21941 Rio De Janeiro, Brazil
[6] Inst Nacl Cardiol, Rio De Janeiro, Brazil
[7] Albert Einstein Coll Med, DP Purpura Dept Neurosci, Bronx, NY 10467 USA
[8] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[9] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10467 USA
基金
美国国家卫生研究院;
关键词
CELL-DERIVED FACTOR-1; NF-KAPPA-B; MURINE MODEL; ENDOTHELIAL-CELLS; TRYPANOSOMA; INFECTION; DISEASE; ADHESION; MACROPHAGES; CHEMOKINES;
D O I
10.1086/653481
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic chagasic cardiomyopathy is a leading cause of heart failure in Latin American countries. About 30% of Trypanosoma cruzi-infected individuals develop this severe symptomatic form of the disease, characterized by intense inflammatory response accompanied by fibrosis in the heart. We performed an extensive microarray analysis of hearts from a mouse model of this disease and identified significant alterations in expression of similar to 12% of the sampled genes. Extensive up-regulations were associated with immune-inflammatory responses (chemokines, adhesion molecules, cathepsins, and major histocompatibility complex molecules) and fibrosis (extracellular matrix components, lysyl oxidase, and tissue inhibitor of metalloproteinase 1). Our results indicate potentially relevant factors involved in the pathogenesis of the disease that may provide new therapeutic targets in chronic Chagas disease.
引用
收藏
页码:416 / 426
页数:11
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