Key result
Trypanosoma cruzi infection of murine cardiomyocytes alters 353 genes linked to inflammation and apoptosis.
Why the study?
Events associated with Trypanosoma cruzi tropism for and invasion of cardiomyocytes have been the focus of intense investigation to understand chronic chagasic cardiomyopathy.
T. cruzi infection induces broad modulations of host cell machinery in primary murine cardiomyocytes, providing insight into the molecular pathogenesis of Chagasic cardiomyopathy.
Does not inform Chagas management; leaves open validation in human cardiomyocytes and in vivo models.
Chagas' disease, caused by the hemoflagellate protozoan Trypanosoma cruzi, affects millions of people in South and Central America. Chronic chagasic cardiomyopathy, the most devastating manifestation of this disease, occurs in approximately one-third of infected individuals. Events associated with the parasite's tropism for and invasion of cardiomyocytes have been the focus of intense investigation in recent years. In the present study, we use murine microarrays to investigate the cellular response caused by invasion of primary murine cardiomyocytes by T. cruzi trypomastigotes. These studies identified 353 murine genes that were differentially expressed during the early stages of invasion and infection of these cells. Genes associated with the immune response, inflammation, cytoskeleton organization, cell-cell and cell-matrix interactions, apoptosis, cell cycle, and oxidative stress are among those affected during the infection. Our data indicate that T. cruzi induces broad modulations of the host cell machinery in ways that provide insight into how the parasite survives, replicates, and persists in the infected host and ultimately defines the clinical outcome of the infection.
No takes yet. Share an insight, caveat, or question.
Manque et al. (2011) studied Trypanosoma cruzi infection (Chagas' disease). Trypanosoma cruzi trypomastigotes vs. Uninfected cardiomyocytes or cardiomyocytes incubated with noninvasive epimastigotes was evaluated on Differentially expressed genes (DEGs) during infection. Trypanosoma cruzi infection of primary murine cardiomyocytes induced the differential expression of 353 genes associated with immune response, inflammation, cytoskeleton organization, and apoptosis.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: