L-proline is essential for the intracellular differentiation of Trypanosoma cruzi
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , , , , |
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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Repositório Institucional da UNIFESP |
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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 |
_version_ |
1814268441451823104 |