Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice.
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFOP |
Texto Completo: | http://www.repositorio.ufop.br/handle/123456789/9897 |
Resumo: | Differently from others Leishmania species, infection by the protozoan parasite L. amazonensis is associated with a lack of antigen-specific T-cell responses. Dendritic cells (DC) are essential for the innate immune response and for directing the differentiation of T-helper lymphocytes. Previously, we showed that L. amazonensis infection impairs DC activation through the activation of adenosine A2B receptor, and here, we evaluated the intracellular events triggered by this receptor in infected cells. To this aim, bone marrow-derived DC from C57BL/6J mice were infected with metacyclic promastigotes of L. amazonensis. Our results show, for the first time, that L. amazonensis increases the production of cAMP and the phosphorylation of extracellular signal-regulated protein kinases 1/2 (ERK1/2) in infected DC by a mechanism dependent on the A2B receptor. Furthermore, L. amazonensis impairs CD40 expression and IL-12 production by DC, and the inhibition of adenylate cyclase, phosphoinositide 3-kinase (PI3K), and ERK1/2 prevent these effects. The increase of ERK1/2 phosphorylation and the inhibition of DC activation by L. amazonensis are independent of protein kinase A (PKA). In addition, C57BL/6J mice were inoculated in the ears with metacyclic promastigotes, in the presence of PSB1115, an A2B receptor antagonist. PSB1115 treatment increases the percentage of CD40+ DC on ears and draining lymph nodes. Furthermore, this treatment reduces lesion size and tissue parasitism. Lymph node cells from treated mice produce higher levels of IFN-γ than control mice, without altering the production of IL-10. In conclusion, we suggest a new pathway used by the parasite (A2B receptor → cAMP → PI3K → ERK1/2) to suppress DC activation, which may contribute to the decrease of IFN-γ production following by the deficiency in immune response characteristic of L. amazonensis infection. |
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Figueiredo, Amanda Braga deTestasicca, Miriam Conceição de SouzaMineo, Tiago Wilson PatriarcaAfonso, Luís Carlos Crocco2018-05-04T13:03:12Z2018-05-04T13:03:12Z2017FIGUEIREDO, A. B. de et al. Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. Frontiers in Immunology, v. 8, p. 849, 2017. Disponível em: <https://www.frontiersin.org/articles/10.3389/fimmu.2017.00849/full>. Acesso em: 05 abr. 2018.16643224http://www.repositorio.ufop.br/handle/123456789/9897Differently from others Leishmania species, infection by the protozoan parasite L. amazonensis is associated with a lack of antigen-specific T-cell responses. Dendritic cells (DC) are essential for the innate immune response and for directing the differentiation of T-helper lymphocytes. Previously, we showed that L. amazonensis infection impairs DC activation through the activation of adenosine A2B receptor, and here, we evaluated the intracellular events triggered by this receptor in infected cells. To this aim, bone marrow-derived DC from C57BL/6J mice were infected with metacyclic promastigotes of L. amazonensis. Our results show, for the first time, that L. amazonensis increases the production of cAMP and the phosphorylation of extracellular signal-regulated protein kinases 1/2 (ERK1/2) in infected DC by a mechanism dependent on the A2B receptor. Furthermore, L. amazonensis impairs CD40 expression and IL-12 production by DC, and the inhibition of adenylate cyclase, phosphoinositide 3-kinase (PI3K), and ERK1/2 prevent these effects. The increase of ERK1/2 phosphorylation and the inhibition of DC activation by L. amazonensis are independent of protein kinase A (PKA). In addition, C57BL/6J mice were inoculated in the ears with metacyclic promastigotes, in the presence of PSB1115, an A2B receptor antagonist. PSB1115 treatment increases the percentage of CD40+ DC on ears and draining lymph nodes. Furthermore, this treatment reduces lesion size and tissue parasitism. Lymph node cells from treated mice produce higher levels of IFN-γ than control mice, without altering the production of IL-10. In conclusion, we suggest a new pathway used by the parasite (A2B receptor → cAMP → PI3K → ERK1/2) to suppress DC activation, which may contribute to the decrease of IFN-γ production following by the deficiency in immune response characteristic of L. amazonensis infection. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. Fonte: o próprio artigo.info:eu-repo/semantics/openAccessExtracellular signal-regulated protein kinasesLeishmania amazonensisLeishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice.info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleengreponame:Repositório Institucional da UFOPinstname:Universidade Federal de Ouro Preto (UFOP)instacron:UFOPLICENSElicense.txtlicense.txttext/plain; charset=utf-8924http://www.repositorio.ufop.br/bitstream/123456789/9897/2/license.txt62604f8d955274beb56c80ce1ee5dcaeMD52ORIGINALARTIGO_LeishmaniaAmazonensisInduced.pdfARTIGO_LeishmaniaAmazonensisInduced.pdfapplication/pdf2635979http://www.repositorio.ufop.br/bitstream/123456789/9897/1/ARTIGO_LeishmaniaAmazonensisInduced.pdf1d8e68595943fcc5f2128db33f860577MD51123456789/98972018-05-04 09:03:12.757oai:localhost: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ório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332018-05-04T13:03:12Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)false |
dc.title.pt_BR.fl_str_mv |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. |
title |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. |
spellingShingle |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. Figueiredo, Amanda Braga de Extracellular signal-regulated protein kinases Leishmania amazonensis |
title_short |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. |
title_full |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. |
title_fullStr |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. |
title_full_unstemmed |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. |
title_sort |
Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. |
author |
Figueiredo, Amanda Braga de |
author_facet |
Figueiredo, Amanda Braga de Testasicca, Miriam Conceição de Souza Mineo, Tiago Wilson Patriarca Afonso, Luís Carlos Crocco |
author_role |
author |
author2 |
Testasicca, Miriam Conceição de Souza Mineo, Tiago Wilson Patriarca Afonso, Luís Carlos Crocco |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Figueiredo, Amanda Braga de Testasicca, Miriam Conceição de Souza Mineo, Tiago Wilson Patriarca Afonso, Luís Carlos Crocco |
dc.subject.por.fl_str_mv |
Extracellular signal-regulated protein kinases Leishmania amazonensis |
topic |
Extracellular signal-regulated protein kinases Leishmania amazonensis |
description |
Differently from others Leishmania species, infection by the protozoan parasite L. amazonensis is associated with a lack of antigen-specific T-cell responses. Dendritic cells (DC) are essential for the innate immune response and for directing the differentiation of T-helper lymphocytes. Previously, we showed that L. amazonensis infection impairs DC activation through the activation of adenosine A2B receptor, and here, we evaluated the intracellular events triggered by this receptor in infected cells. To this aim, bone marrow-derived DC from C57BL/6J mice were infected with metacyclic promastigotes of L. amazonensis. Our results show, for the first time, that L. amazonensis increases the production of cAMP and the phosphorylation of extracellular signal-regulated protein kinases 1/2 (ERK1/2) in infected DC by a mechanism dependent on the A2B receptor. Furthermore, L. amazonensis impairs CD40 expression and IL-12 production by DC, and the inhibition of adenylate cyclase, phosphoinositide 3-kinase (PI3K), and ERK1/2 prevent these effects. The increase of ERK1/2 phosphorylation and the inhibition of DC activation by L. amazonensis are independent of protein kinase A (PKA). In addition, C57BL/6J mice were inoculated in the ears with metacyclic promastigotes, in the presence of PSB1115, an A2B receptor antagonist. PSB1115 treatment increases the percentage of CD40+ DC on ears and draining lymph nodes. Furthermore, this treatment reduces lesion size and tissue parasitism. Lymph node cells from treated mice produce higher levels of IFN-γ than control mice, without altering the production of IL-10. In conclusion, we suggest a new pathway used by the parasite (A2B receptor → cAMP → PI3K → ERK1/2) to suppress DC activation, which may contribute to the decrease of IFN-γ production following by the deficiency in immune response characteristic of L. amazonensis infection. |
publishDate |
2017 |
dc.date.issued.fl_str_mv |
2017 |
dc.date.accessioned.fl_str_mv |
2018-05-04T13:03:12Z |
dc.date.available.fl_str_mv |
2018-05-04T13:03:12Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
FIGUEIREDO, A. B. de et al. Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. Frontiers in Immunology, v. 8, p. 849, 2017. Disponível em: <https://www.frontiersin.org/articles/10.3389/fimmu.2017.00849/full>. Acesso em: 05 abr. 2018. |
dc.identifier.uri.fl_str_mv |
http://www.repositorio.ufop.br/handle/123456789/9897 |
dc.identifier.issn.none.fl_str_mv |
16643224 |
identifier_str_mv |
FIGUEIREDO, A. B. de et al. Leishmania amazonensis-induced caMP triggered by adenosine a2B receptor is important to inhibit dendritic cell activation and evade immune response in infected mice. Frontiers in Immunology, v. 8, p. 849, 2017. Disponível em: <https://www.frontiersin.org/articles/10.3389/fimmu.2017.00849/full>. Acesso em: 05 abr. 2018. 16643224 |
url |
http://www.repositorio.ufop.br/handle/123456789/9897 |
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eng |
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