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Mauro Cortez

Researcher at University of São Paulo

Publications -  38
Citations -  1237

Mauro Cortez is an academic researcher from University of São Paulo. The author has contributed to research in topics: Trypanosoma cruzi & Leishmania. The author has an hindex of 18, co-authored 36 publications receiving 1060 citations. Previous affiliations of Mauro Cortez include University of Maryland, College Park & University of Antofagasta.

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Journal ArticleDOI

Trypanosoma cruzi subverts the sphingomyelinase-mediated plasma membrane repair pathway for cell invasion

TL;DR: It is shown that host cell entry by T. cruzi mimics a process of plasma membrane injury and repair that involves Ca(2+)-dependent exocytosis of lysosomes, delivery of acid sphingomyelinase to the outer leaflet of the plasma membrane, and a rapid form of endocytoses that internalizes membrane lesions.
Journal ArticleDOI

Caveolae internalization repairs wounded cells and muscle fibers.

TL;DR: This work shows that muscle fibers and other cell types repair membrane wounds by a mechanism involving Ca2+-triggered exocytosis of lysosomes, release of acid sphingomyelinase, and rapid lesion removal by caveolar endocyTosis, providing a mechanistic explanation for the muscle pathology associated with mutations in caveolae proteins.
Journal ArticleDOI

Iron uptake controls the generation of Leishmania infective forms through regulation of ROS levels

TL;DR: Iron uptake promotes hydrogen peroxide–dependent differentiation of Leishmania promastigote into infective amastigotes into infectives amastsigotes.
Book ChapterDOI

Trypanosoma cruzi: Parasite and Host Cell Signaling during the Invasion Process

TL;DR: The mechanisms of host cell invasion by T. cruzi have been partially elucidated and surface molecules that bind to host cells as a prelude to invasion appear to be devoid of signaling properties, but they may induce TCT enzymes, such as oligopeptidase B and cruzipain, to generate Ca2+ signaling factors of parasite or host cell origin.
Journal ArticleDOI

Involvement of Trypanosoma cruzi metacyclic trypomastigote surface molecule gp82 in adhesion to gastric mucin and invasion of epithelial cells.

TL;DR: It is suggested that gp82 mediates the interaction of metacyclic trypomastigote surface molecule gp90 or gp35/50 with gastric mucin and the subsequent penetration of underlying epithelial cells.