Centro de Altos Estudios en Ciencias Humanas y de la Salud

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Browsing Centro de Altos Estudios en Ciencias Humanas y de la Salud by Author "Bustos, Patricia Laura"
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    Improved Immuno-Detection of a Low-Abundance Cyclophilin Allows the Confirmation of its Expression in a Protozoan Parasite
    (Immunochemistry & Inmunopathology, 2015) Bustos, Patricia Laura ; Perrone, Alina E ; Milduberger, Natalia A. ; Bua, Jaqueline
    Protein samples can be challenging to analyze due to the presence of high-abundance proteins masking low-abundance proteins of interest, such as biomarkers and novel physiological mediators. Cyclophilins are chaperones involved in the cis/trans isomerization of peptidyl-prolyl bonds in peptides or proteins and have been found in every organism sequenced to date. Although considerable progress has been made in the characterization of some cyclophilins expressed in diverse parasites invading humans, the main aspects of low-abundance members of this family remain unknown. In the present work, we present that the combined strategy of using more specific antibodies and increasing the presence of subcellular proteins in the sample, allowed us to confirm the expression of a 21.1 kDa cyclophilin for the first time in Trypanosoma cruzi.
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    Mitochondrial permeability transition in protozoan parasites: what we learned from Trypanosoma cruzi
    (Official journal of the Cell Death Differentiation Association, 2017-9-21) Bustos, Patricia Laura ; Perrone, Alina E ; Milduberger, Natalia A. ; Bua, Jaqueline
    Regulated cell death (RCD) involves a genetically encoded molecular machinery, which can be altered by means of pharmacologic and/or genetics interventions targeting the key components of such machinery. A variant of RCD that often manifests with necrotic morphotype critically relies on Cyclophilin D (CyPD), a mitochondrial matrix peptidyl-prolyl isomerase, which is encoded by the Ppif gene. A lot a research has been done in mammals, but still very little is known for protozoan parasites, one of the most ancient phylogenic branches of unicellular eukaryotes. In the present work, we revised the knowledge about mitochondrial permeability transition and regulated cell death in the parasite Trypanosoma cruzi, the causative agent of Chagas disease, that affects 7?8 million people only in South America as well as in other parts of the world through migrations from endemic areas. We also included other protozoan parasites of medical importance to briefly summarize and compare what is known so far about this exciting field of parasitology. We finalized the present article explaining the finding that a homologue of Cyclophilin D, which is the unique genetically confirmed regulator of the mitochondrial permeability transition in mammalian cells, is also expressed in T. cruzi and may be involved in regulated cell death in the parasite. These results were published earlier this year in Cell Death Discovery (Cell Death Discov 3, 16092. 2017 Feb 06). To our knowledge, this is the only Cyclophilin D homologue that has been described in a protozoan parasite. We consider that this parasite mitochondrial cyclophilin could be a valuable drug target for the therapeutic of Chagas disease.