The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis

Detalhes bibliográficos
Autor(a) principal: Cardoso, A
Data de Publicação: 2018
Outros Autores: Castro, A, Martins, AC, Carriche, GM, Murigneux, V, Castro, I, Cumano, A, Vieira, P, Saraiva, M
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/126496
Resumo: Inflammatory bowel disease encompasses a group of chronic-inflammatory conditions of the colon and small intestine. These conditions are characterized by exacerbated inflammation of the organ that greatly affects the quality of life of patients. Molecular mechanisms counteracting this hyperinflammatory status of the gut offer strategies for therapeutic intervention. Among these regulatory molecules is the anti-inflammatory cytokine interleukin (IL)-10, as shown in mice and humans. Indeed, IL-10 signaling, particularly in macrophages, is essential for intestinal homeostasis. We sought to investigate the temporal profile of IL-10-mediated protection during chemical colitis and which were the underlying mechanisms. Using a novel mouse model of inducible IL-10 overexpression (pMT-10), described here, we show that mice preconditioned with IL-10 for 8 days before dextran sulfate sodium (DSS) administration developed a milder colitic phenotype. In IL-10-induced colitic mice, Ly6C cells isolated from the lamina propria showed a decreased inflammatory profile. Because our mouse model leads to transcription of the IL-10 transgene in the bone marrow and elevated seric IL-10 concentration, we investigated whether IL-10 could imprint immune cells in a long-lasting way, thus conferring sustained protection to colitis. We show that this was not the case, as IL-10-afforded protection was only observed if IL-10 induction immediately preceded DSS-mediated colitis. Thus, despite the protection afforded by IL-10 in colitis, novel strategies are required, specifically to achieve long-lasting protection.
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spelling The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitisColitisInflammationInterleukin-10MacrophagesTherapyInflammatory bowel disease encompasses a group of chronic-inflammatory conditions of the colon and small intestine. These conditions are characterized by exacerbated inflammation of the organ that greatly affects the quality of life of patients. Molecular mechanisms counteracting this hyperinflammatory status of the gut offer strategies for therapeutic intervention. Among these regulatory molecules is the anti-inflammatory cytokine interleukin (IL)-10, as shown in mice and humans. Indeed, IL-10 signaling, particularly in macrophages, is essential for intestinal homeostasis. We sought to investigate the temporal profile of IL-10-mediated protection during chemical colitis and which were the underlying mechanisms. Using a novel mouse model of inducible IL-10 overexpression (pMT-10), described here, we show that mice preconditioned with IL-10 for 8 days before dextran sulfate sodium (DSS) administration developed a milder colitic phenotype. In IL-10-induced colitic mice, Ly6C cells isolated from the lamina propria showed a decreased inflammatory profile. Because our mouse model leads to transcription of the IL-10 transgene in the bone marrow and elevated seric IL-10 concentration, we investigated whether IL-10 could imprint immune cells in a long-lasting way, thus conferring sustained protection to colitis. We show that this was not the case, as IL-10-afforded protection was only observed if IL-10 induction immediately preceded DSS-mediated colitis. Thus, despite the protection afforded by IL-10 in colitis, novel strategies are required, specifically to achieve long-lasting protection.Frontiers Media20182018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/126496eng1664-322410.3389/fimmu.2018.00400Cardoso, ACastro, AMartins, ACCarriche, GMMurigneux, VCastro, ICumano, AVieira, PSaraiva, Minfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-26T15:03:40ZPortal AgregadorONG
dc.title.none.fl_str_mv The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
title The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
spellingShingle The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
Cardoso, A
Colitis
Inflammation
Interleukin-10
Macrophages
Therapy
title_short The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
title_full The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
title_fullStr The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
title_full_unstemmed The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
title_sort The Dynamics of Interleukin-10-afforded protection during dextran sulfate sodium-induced colitis
author Cardoso, A
author_facet Cardoso, A
Castro, A
Martins, AC
Carriche, GM
Murigneux, V
Castro, I
Cumano, A
Vieira, P
Saraiva, M
author_role author
author2 Castro, A
Martins, AC
Carriche, GM
Murigneux, V
Castro, I
Cumano, A
Vieira, P
Saraiva, M
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Cardoso, A
Castro, A
Martins, AC
Carriche, GM
Murigneux, V
Castro, I
Cumano, A
Vieira, P
Saraiva, M
dc.subject.por.fl_str_mv Colitis
Inflammation
Interleukin-10
Macrophages
Therapy
topic Colitis
Inflammation
Interleukin-10
Macrophages
Therapy
description Inflammatory bowel disease encompasses a group of chronic-inflammatory conditions of the colon and small intestine. These conditions are characterized by exacerbated inflammation of the organ that greatly affects the quality of life of patients. Molecular mechanisms counteracting this hyperinflammatory status of the gut offer strategies for therapeutic intervention. Among these regulatory molecules is the anti-inflammatory cytokine interleukin (IL)-10, as shown in mice and humans. Indeed, IL-10 signaling, particularly in macrophages, is essential for intestinal homeostasis. We sought to investigate the temporal profile of IL-10-mediated protection during chemical colitis and which were the underlying mechanisms. Using a novel mouse model of inducible IL-10 overexpression (pMT-10), described here, we show that mice preconditioned with IL-10 for 8 days before dextran sulfate sodium (DSS) administration developed a milder colitic phenotype. In IL-10-induced colitic mice, Ly6C cells isolated from the lamina propria showed a decreased inflammatory profile. Because our mouse model leads to transcription of the IL-10 transgene in the bone marrow and elevated seric IL-10 concentration, we investigated whether IL-10 could imprint immune cells in a long-lasting way, thus conferring sustained protection to colitis. We show that this was not the case, as IL-10-afforded protection was only observed if IL-10 induction immediately preceded DSS-mediated colitis. Thus, despite the protection afforded by IL-10 in colitis, novel strategies are required, specifically to achieve long-lasting protection.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018-01-01T00:00:00Z
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.uri.fl_str_mv https://hdl.handle.net/10216/126496
url https://hdl.handle.net/10216/126496
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1664-3224
10.3389/fimmu.2018.00400
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Frontiers Media
publisher.none.fl_str_mv Frontiers Media
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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