Literature DB >> 10425154

Trypanosoma cruzi: characterization of an intracellular epimastigote-like form.

M Almeida-de-Faria1, E Freymüller, W Colli, M J Alves.   

Abstract

Almeida-de-Faria, M., Freymüller, E., Colli, W., and Alves, M. J. M. 1999. Trypanosoma cruzi: Characterization of an intracellular epimastigote-like form. Experimental Parasitology 92, 263-274. A detailed study of transient epimastigote-like forms as intermediates in the differentiation of Trypanosoma cruzi amastigotes to trypomastigotes inside the host cell cytoplasm was undertaken using the CL-14 clone grown in cells maintained at 33 degrees C. Several parameters related to these forms have been compared with epimastigotes and other stages of the parasite. Consequently, the designation of intracellular epimastigotes is proposed for these forms. Despite being five times shorter (5.4 +/- 0.7 micrometer) than the extracellular epimastigote (25.2 +/- 2.1 micrometer), the overall morphology of the intracellular epimastigote is very similar to a bona fide epimastigote, when cell shape, position, and general aspect of organelles are compared by transmission electron microscopy. Epimastigotes from both sources are lysed by human complement and bind to DEAE-cellulose, in contrast to amastigotes and trypomastigote forms. A monoclonal antibody (3C5) reacts with both epimastigotes either isolated from axenic media or intracellular and very faintly with amastigotes, but not with trypomastigotes. Some differences of a quantitative nature are apparent between the two epimastigote forms when reactivities with lectins or stage-specific antibodies are compared, revealing the transient nature of the intracellular epimastigote. The epitope recognized by 3C5 monoclonal antibody reacts slightly more intensely with extracellular than with intracellular epimastigotes, as detected by immunoelectron microscopy. Also a very faint reaction of the intracellular epimastigotes was observed with monoclonal antibody 2C2, an antibody which recognizes a glycoprotein specific for the amastigote stage. Biological parameters as growth curves in axenic media and inhability to invade nonphagocytic tissue-cultured cells are similar in the epimastigotes from both origins. It is proposed that the epimastigote-like forms are an obligatory transitional stage in the transformation of amastigotes to trypomastigotes with a variable time of permanency in the host cell cytoplasm depending on environmental conditions. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10425154     DOI: 10.1006/expr.1999.4423

Source DB:  PubMed          Journal:  Exp Parasitol        ISSN: 0014-4894            Impact factor:   2.011


  13 in total

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Authors:  K G Khusal; R R Tonelli; E C Mattos; C O Soares; B M Di Genova; M A Juliano; U Urias; W Colli; M J M Alves
Journal:  Parasitol Res       Date:  2014-10-17       Impact factor: 2.289

Review 2.  Enucleated L929 cells support invasion, differentiation, and multiplication of Trypanosoma cruzi parasites.

Authors:  Vanessa C Coimbra; Denise Yamamoto; Ketna G Khusal; Vanessa Diniz Atayde; Maria Cecília Fernandes; Renato A Mortara; Nobuko Yoshida; Maria Julia M Alves; Michel Rabinovitch
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3.  The Involvement of Glutamate Metabolism in the Resistance to Thermal, Nutritional, and Oxidative Stress in Trypanosoma cruzi.

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4.  The glutamine synthetase of Trypanosoma cruzi is required for its resistance to ammonium accumulation and evasion of the parasitophorous vacuole during host-cell infection.

Authors:  Marcell Crispim; Flávia Silva Damasceno; Agustín Hernández; María Julia Barisón; Ismael Pretto Sauter; Raphael Souza Pavani; Alexandre Santos Moura; Elizabeth Mieko Furusho Pral; Mauro Cortez; Maria Carolina Elias; Ariel Mariano Silber
Journal:  PLoS Negl Trop Dis       Date:  2018-01-10

5.  Improved method for in vitro secondary amastigogenesis of Trypanosoma cruzi: morphometrical and molecular analysis of intermediate developmental forms.

Authors:  L A Hernández-Osorio; C Márquez-Dueñas; L E Florencio-Martínez; G Ballesteros-Rodea; S Martínez-Calvillo; R G Manning-Cela
Journal:  J Biomed Biotechnol       Date:  2009-12-13

6.  A Fluorinated Phenylbenzothiazole Arrests the Trypanosoma cruzi Cell Cycle and Diminishes the Infection of Mammalian Host Cells.

Authors:  Roberto I Cuevas-Hernández; Richard M B M Girard; Sarai Martínez-Cerón; Marcelo Santos da Silva; Maria Carolina Elias; Marcell Crispim; José G Trujillo-Ferrara; Ariel Mariano Silber
Journal:  Antimicrob Agents Chemother       Date:  2020-01-27       Impact factor: 5.191

7.  Actions of a proline analogue, L-thiazolidine-4-carboxylic acid (T4C), on Trypanosoma cruzi.

Authors:  Anahí Magdaleno; Il-Young Ahn; Lisvane Silva Paes; Ariel M Silber
Journal:  PLoS One       Date:  2009-02-20       Impact factor: 3.240

8.  Proline dehydrogenase regulates redox state and respiratory metabolism in Trypanosoma cruzi.

Authors:  Lisvane Silva Paes; Brian Suárez Mantilla; Flávia Menezes Zimbres; Elisabeth Mieko Furusho Pral; Patrícia Diogo de Melo; Erich B Tahara; Alicia J Kowaltowski; Maria Carolina Elias; Ariel Mariano Silber
Journal:  PLoS One       Date:  2013-07-22       Impact factor: 3.240

9.  Memantine, an antagonist of the NMDA glutamate receptor, affects cell proliferation, differentiation and the intracellular cycle and induces apoptosis in Trypanosoma cruzi.

Authors:  Flávia Silva Damasceno; María Julia Barisón; Elisabeth Mieko Furusho Pral; Lisvane Silva Paes; Ariel Mariano Silber
Journal:  PLoS Negl Trop Dis       Date:  2014-02-27

Review 10.  The Uptake and Metabolism of Amino Acids, and Their Unique Role in the Biology of Pathogenic Trypanosomatids.

Authors:  Letícia Marchese; Janaina de Freitas Nascimento; Flávia Silva Damasceno; Frédéric Bringaud; Paul A M Michels; Ariel Mariano Silber
Journal:  Pathogens       Date:  2018-04-01
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