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Mir-190b negatively contributes to the Trypanosoma cruzi -infected cell survival by repressing PTEN protein expression
Chagas disease, which is caused by the intracellular protozoan Trypanosoma cruzi , is a serious health problem in Latin America. The heart is one of the major organs affected by this parasitic infection. The pathogenesis of tissue remodelling, particularly regarding cardiomyocyte behaviour after par...
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Published in: | Memórias do Instituto Oswaldo Cruz 2016-07, Vol.110 (8) |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Chagas disease, which is caused by the intracellular protozoan
Trypanosoma cruzi , is a serious health problem in Latin America. The
heart is one of the major organs affected by this parasitic infection.
The pathogenesis of tissue remodelling, particularly regarding
cardiomyocyte behaviour after parasite infection, and the molecular
mechanisms that occur immediately following parasite entry into host
cells are not yet completely understood. Previous studies have reported
that the establishment of parasitism is connected to the activation of
the phosphatidylinositol- 3 kinase (PI3K), which controls important
steps in cellular metabolism by regulating the production of the second
messenger phosphatidylinositol-3,4,5-trisphosphate. Particularly, the
tumour suppressor PTEN is a negative regulator of PI3K signalling.
However, mechanistic details of the modulatory activity of PTEN on
Chagas disease have not been elucidated. To address this question, H9c2
cells were infected with T. cruzi Berenice 62 strain and the expression
of a specific set of microRNAs (miRNAs) were investigated. Our cellular
model demonstrated that miRNA-190b is correlated to the decrease of
cellular viability rates by negatively modulating PTEN protein
expression in T. cruzi-infected cells. |
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ISSN: | 1678-8060 |