Caspase 8 inhibition increases the infection with trypanosoma cruzi in thehuman trophoblast cell line (bewo)
Author
dc.contributor.author
Carrillo, Ileana
Author
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Castillo, Christian
Author
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Droguett, Daniel
Author
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Muñoz, Lorena
Author
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Liempi, Ana
Author
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Maya Arango, Juan
Author
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Galanti Garrone, Norbel
Author
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Kemmerling Weis, Ulrike
Admission date
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2017-03-02T14:01:49Z
Available date
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2017-03-02T14:01:49Z
Publication date
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2016
Cita de ítem
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Placenta. Volumen: 45 Páginas: 95-95 Abstract de reunión: P1.75
es_ES
Identifier
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1532-3102
Identifier
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https://repositorio.uchile.cl/handle/2250/142932
Abstract
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Congenital Chagas’ disease is caused by the haemophlagelated protozoan
Trypanosoma cruzi (T. cruzi), which is able to cross the placental barrier and
infect both the placenta and fetus. However, congenital transmission rates
are low, suggesting the presence of local defense mechanisms. The
trophoblast is the first tissue of the placental barrier in contact with the
maternal blood; its epithelial turnover is considered part of innate immune
system. Previous studies have shown that T. cruzi induces proliferation,
differentiation and apoptosis in the trophoblast, suggesting an
increase in epithelial turnover. Caspase 8 is an essential molecule not only
during apoptotic cell death but also during trophoblast differentiation.