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Ultrastructural Expansion Microscopy in Three In Vitro Life Cycle Stages of Trypanosoma cruzi.
de Hernández, María Azul; Martinez Peralta, Gonzalo; Vena, Rodrigo; Alonso, Victoria Lucia.
Afiliação
  • de Hernández MA; Instituto de Biología Molecular y Celular de Rosario (IBR), CONICET.
  • Martinez Peralta G; Instituto de Biología Molecular y Celular de Rosario (IBR), CONICET; Area Biología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario (UNR).
  • Vena R; Instituto de Biología Molecular y Celular de Rosario (IBR), CONICET; Unidad de Microscopía, Instituto de Biología Molecular y Celular de Rosario (IBR), CONICET.
  • Alonso VL; Instituto de Biología Molecular y Celular de Rosario (IBR), CONICET; Area Parasitología, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario (UNR); Unidad de Microscopía, Instituto de Biología Molecular y Celular de Rosario (IBR), CONICET; alonso@ibr-conicet.gov.ar.
J Vis Exp ; (195)2023 05 12.
Article em En | MEDLINE | ID: mdl-37246875
We describe here the application of ultrastructure expansion microscopy (U-ExM) in Trypanosoma cruzi, a technique that allows increasing the spatial resolution of a cell or tissue for microscopic imaging. This is performed by physically expanding a sample with off-the-shelf chemicals and common lab equipment. Chagas disease is a widespread and pressing public health concern caused by T. cruzi. The disease is prevalent in Latin America and has become a significant problem in non-endemic regions due to increased migration. The transmission of T. cruzi occurs through hematophagous insect vectors belonging to the Reduviidae and Hemiptera families. Following infection, T. cruzi amastigotes multiply within the mammalian host and differentiate into trypomastigotes, the non-replicative bloodstream form. In the insect vector, trypomastigotes transform into epimastigotes and proliferate through binary fission.The differentiation between the life cycle stages requires an extensive rearrangement of the cytoskeleton and can be recreated in the lab completely using different cell culture techniques. We describe here a detailed protocol for the application of U-ExM in three in vitro life cycle stages of Trypanosoma cruzi, focusing on optimization of the immunolocalization of cytoskeletal proteins. We also optimized the use of N-Hydroxysuccinimide ester (NHS), a pan-proteome label that has enabled us to mark different parasite structures.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma cruzi / Doença de Chagas Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma cruzi / Doença de Chagas Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article