L-proline is essential for the intracellular differentiation of Trypanosoma cruzi

Detalhes bibliográficos
Autor(a) principal: Tonelli, Renata R.
Data de Publicação: 2004
Outros Autores: Silber, Ariel M., Almeida-de-Faria, Martinez, Hirata, Izaura Y. [UNIFESP], Colli, Walter, Alves, Maria Julia M
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1111/j.1462-5822.2004.00397.x
http://repositorio.unifesp.br/handle/11600/27843
Resumo: Using as the host cell, a proline-requiring mutant of Chinese hamster ovary cell (CHO-K1), it was possible to arrest the differentiation of amastigote forms of Trypanosoma cruzi at the intermediate intracellular epimastigote-like stage. Complete differentiation to the trypomastigote stage was obtained by addition of L-proline to the medium. This effect was more pronounced using the T. cruzi CL-14 clone that differentiates fully at 33degreesC (permissive temperature) and poorly at 37degreesC (restrictive temperature). A synchronous differentiation of T. cruzi inside the host-cell is then possible by temperature switching in the presence of proline. It was found that differentiation of intracellular epimastigotes and trypomastigote bursting were proline concentration dependent. the intracellular concentration of proline was measured as well as the transport capacity of proline by each stage of the parasite. Amastigotes have the highest concentration of free proline (8.09 +/- 1.46 mM) when compared to trypomastigotes (3.81 +/- 1.55) or intracellular epimastigote-like forms (0.45 +/- 0.06 mM). in spite of having the lowest content of intracellular free proline, intracellular epimastigotes maintained the highest levels of L-proline transport compared to trypomastigotes and intracellular amastigotes, providing evidence for a high turnover for the L-proline pool in that parasite stage. This is the first report to establish a relationship between proline concentration and intracellular differentiation of Trypanosoma cruzi in the mammalian host.
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spelling L-proline is essential for the intracellular differentiation of Trypanosoma cruziUsing as the host cell, a proline-requiring mutant of Chinese hamster ovary cell (CHO-K1), it was possible to arrest the differentiation of amastigote forms of Trypanosoma cruzi at the intermediate intracellular epimastigote-like stage. Complete differentiation to the trypomastigote stage was obtained by addition of L-proline to the medium. This effect was more pronounced using the T. cruzi CL-14 clone that differentiates fully at 33degreesC (permissive temperature) and poorly at 37degreesC (restrictive temperature). A synchronous differentiation of T. cruzi inside the host-cell is then possible by temperature switching in the presence of proline. It was found that differentiation of intracellular epimastigotes and trypomastigote bursting were proline concentration dependent. the intracellular concentration of proline was measured as well as the transport capacity of proline by each stage of the parasite. Amastigotes have the highest concentration of free proline (8.09 +/- 1.46 mM) when compared to trypomastigotes (3.81 +/- 1.55) or intracellular epimastigote-like forms (0.45 +/- 0.06 mM). in spite of having the lowest content of intracellular free proline, intracellular epimastigotes maintained the highest levels of L-proline transport compared to trypomastigotes and intracellular amastigotes, providing evidence for a high turnover for the L-proline pool in that parasite stage. This is the first report to establish a relationship between proline concentration and intracellular differentiation of Trypanosoma cruzi in the mammalian host.Univ São Paulo, Dept Bioquim, Inst Quim, BR-05513970 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biofis, BR-05513970 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biofis, BR-05513970 São Paulo, BrazilWeb of ScienceBlackwell Publishing LtdUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Tonelli, Renata R.Silber, Ariel M.Almeida-de-Faria, MartinezHirata, Izaura Y. [UNIFESP]Colli, WalterAlves, Maria Julia M2016-01-24T12:37:16Z2016-01-24T12:37:16Z2004-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion733-741http://dx.doi.org/10.1111/j.1462-5822.2004.00397.xCellular Microbiology. Oxford: Blackwell Publishing Ltd, v. 6, n. 8, p. 733-741, 2004.10.1111/j.1462-5822.2004.00397.x1462-5814http://repositorio.unifesp.br/handle/11600/27843WOS:000222462200004engCellular Microbiologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T10:37:16Zoai:repositorio.unifesp.br/:11600/27843Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T10:37:16Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
title L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
spellingShingle L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
Tonelli, Renata R.
title_short L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
title_full L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
title_fullStr L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
title_full_unstemmed L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
title_sort L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
author Tonelli, Renata R.
author_facet Tonelli, Renata R.
Silber, Ariel M.
Almeida-de-Faria, Martinez
Hirata, Izaura Y. [UNIFESP]
Colli, Walter
Alves, Maria Julia M
author_role author
author2 Silber, Ariel M.
Almeida-de-Faria, Martinez
Hirata, Izaura Y. [UNIFESP]
Colli, Walter
Alves, Maria Julia M
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Tonelli, Renata R.
Silber, Ariel M.
Almeida-de-Faria, Martinez
Hirata, Izaura Y. [UNIFESP]
Colli, Walter
Alves, Maria Julia M
description Using as the host cell, a proline-requiring mutant of Chinese hamster ovary cell (CHO-K1), it was possible to arrest the differentiation of amastigote forms of Trypanosoma cruzi at the intermediate intracellular epimastigote-like stage. Complete differentiation to the trypomastigote stage was obtained by addition of L-proline to the medium. This effect was more pronounced using the T. cruzi CL-14 clone that differentiates fully at 33degreesC (permissive temperature) and poorly at 37degreesC (restrictive temperature). A synchronous differentiation of T. cruzi inside the host-cell is then possible by temperature switching in the presence of proline. It was found that differentiation of intracellular epimastigotes and trypomastigote bursting were proline concentration dependent. the intracellular concentration of proline was measured as well as the transport capacity of proline by each stage of the parasite. Amastigotes have the highest concentration of free proline (8.09 +/- 1.46 mM) when compared to trypomastigotes (3.81 +/- 1.55) or intracellular epimastigote-like forms (0.45 +/- 0.06 mM). in spite of having the lowest content of intracellular free proline, intracellular epimastigotes maintained the highest levels of L-proline transport compared to trypomastigotes and intracellular amastigotes, providing evidence for a high turnover for the L-proline pool in that parasite stage. This is the first report to establish a relationship between proline concentration and intracellular differentiation of Trypanosoma cruzi in the mammalian host.
publishDate 2004
dc.date.none.fl_str_mv 2004-08-01
2016-01-24T12:37:16Z
2016-01-24T12:37:16Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1111/j.1462-5822.2004.00397.x
Cellular Microbiology. Oxford: Blackwell Publishing Ltd, v. 6, n. 8, p. 733-741, 2004.
10.1111/j.1462-5822.2004.00397.x
1462-5814
http://repositorio.unifesp.br/handle/11600/27843
WOS:000222462200004
url http://dx.doi.org/10.1111/j.1462-5822.2004.00397.x
http://repositorio.unifesp.br/handle/11600/27843
identifier_str_mv Cellular Microbiology. Oxford: Blackwell Publishing Ltd, v. 6, n. 8, p. 733-741, 2004.
10.1111/j.1462-5822.2004.00397.x
1462-5814
WOS:000222462200004
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Cellular Microbiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 733-741
dc.publisher.none.fl_str_mv Blackwell Publishing Ltd
publisher.none.fl_str_mv Blackwell Publishing Ltd
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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