Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model
- Autores
- Iraporda, Carolina; Romanin, David Emmanuel; Bengoa, Ana Agustina; Errea, Agustina Juliana; Cayet, D.; Foligné, B.; Sirard, J.-C.; Garrote, Graciela Liliana; Abraham, Analía Graciela; Rumbo, Martín
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Lactate has long been considered as a metabolic by-product of cells. Recently, this view has been changed by the observation that lactate can act as a signaling molecule and regulates critical functions of the immune system. We previously identified lactate as the component responsible for the modulation of innate immune epithelial response of fermented milk supernatants in vitro. We have also shown that lactate downregulates proinflammatory responses of macrophages and dendritic cells. So far, in vivo effects of lactate on intestinal inflammation have not been reported. We evaluated the effect of intrarectal administration of lactate in a murine model of colitis induced by 2,4,6-trinitrobenzenesulfonic acid (TNBS). The increase in lactate concentration in colon promoted protective effects against TNBS-induced colitis preventing histopathological damage, as well as bacterial translocation and rise of IL-6 levels in serum. Using intestinal epithelial reporter cells, we found that flagellin treatment induced reporter gene expression, which was abrogated by lactate treatment as well as by glycolysis inhibitors. Furthermore, lactate treatment modulated glucose uptake, indicating that high levels of extracellular lactate can impair metabolic reprograming induced by proinflammatory activation. These results suggest that lactate could be a potential beneficial microbiota metabolite and may constitute an overlooked effector with modulatory properties.
Centro de Investigación y Desarrollo en Criotecnología de Alimentos
Instituto de Estudios Inmunológicos y Fisiopatológicos - Materia
-
Ciencias Exactas
Flagellin
Immunomodulation
Innate immunity
Lactate
TNBS-induced colitis - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/86913
Ver los metadatos del registro completo
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Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis modelIraporda, CarolinaRomanin, David EmmanuelBengoa, Ana AgustinaErrea, Agustina JulianaCayet, D.Foligné, B.Sirard, J.-C.Garrote, Graciela LilianaAbraham, Analía GracielaRumbo, MartínCiencias ExactasFlagellinImmunomodulationInnate immunityLactateTNBS-induced colitisLactate has long been considered as a metabolic by-product of cells. Recently, this view has been changed by the observation that lactate can act as a signaling molecule and regulates critical functions of the immune system. We previously identified lactate as the component responsible for the modulation of innate immune epithelial response of fermented milk supernatants in vitro. We have also shown that lactate downregulates proinflammatory responses of macrophages and dendritic cells. So far, in vivo effects of lactate on intestinal inflammation have not been reported. We evaluated the effect of intrarectal administration of lactate in a murine model of colitis induced by 2,4,6-trinitrobenzenesulfonic acid (TNBS). The increase in lactate concentration in colon promoted protective effects against TNBS-induced colitis preventing histopathological damage, as well as bacterial translocation and rise of IL-6 levels in serum. Using intestinal epithelial reporter cells, we found that flagellin treatment induced reporter gene expression, which was abrogated by lactate treatment as well as by glycolysis inhibitors. Furthermore, lactate treatment modulated glucose uptake, indicating that high levels of extracellular lactate can impair metabolic reprograming induced by proinflammatory activation. These results suggest that lactate could be a potential beneficial microbiota metabolite and may constitute an overlooked effector with modulatory properties.Centro de Investigación y Desarrollo en Criotecnología de AlimentosInstituto de Estudios Inmunológicos y Fisiopatológicos2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/86913enginfo:eu-repo/semantics/altIdentifier/issn/1664-3224info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2016.00651info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:16:50Zoai:sedici.unlp.edu.ar:10915/86913Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:16:50.383SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model |
title |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model |
spellingShingle |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model Iraporda, Carolina Ciencias Exactas Flagellin Immunomodulation Innate immunity Lactate TNBS-induced colitis |
title_short |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model |
title_full |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model |
title_fullStr |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model |
title_full_unstemmed |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model |
title_sort |
Local treatment with lactate prevents intestinal inflammation in the TNBS-induced colitis model |
dc.creator.none.fl_str_mv |
Iraporda, Carolina Romanin, David Emmanuel Bengoa, Ana Agustina Errea, Agustina Juliana Cayet, D. Foligné, B. Sirard, J.-C. Garrote, Graciela Liliana Abraham, Analía Graciela Rumbo, Martín |
author |
Iraporda, Carolina |
author_facet |
Iraporda, Carolina Romanin, David Emmanuel Bengoa, Ana Agustina Errea, Agustina Juliana Cayet, D. Foligné, B. Sirard, J.-C. Garrote, Graciela Liliana Abraham, Analía Graciela Rumbo, Martín |
author_role |
author |
author2 |
Romanin, David Emmanuel Bengoa, Ana Agustina Errea, Agustina Juliana Cayet, D. Foligné, B. Sirard, J.-C. Garrote, Graciela Liliana Abraham, Analía Graciela Rumbo, Martín |
author2_role |
author author author author author author author author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Flagellin Immunomodulation Innate immunity Lactate TNBS-induced colitis |
topic |
Ciencias Exactas Flagellin Immunomodulation Innate immunity Lactate TNBS-induced colitis |
dc.description.none.fl_txt_mv |
Lactate has long been considered as a metabolic by-product of cells. Recently, this view has been changed by the observation that lactate can act as a signaling molecule and regulates critical functions of the immune system. We previously identified lactate as the component responsible for the modulation of innate immune epithelial response of fermented milk supernatants in vitro. We have also shown that lactate downregulates proinflammatory responses of macrophages and dendritic cells. So far, in vivo effects of lactate on intestinal inflammation have not been reported. We evaluated the effect of intrarectal administration of lactate in a murine model of colitis induced by 2,4,6-trinitrobenzenesulfonic acid (TNBS). The increase in lactate concentration in colon promoted protective effects against TNBS-induced colitis preventing histopathological damage, as well as bacterial translocation and rise of IL-6 levels in serum. Using intestinal epithelial reporter cells, we found that flagellin treatment induced reporter gene expression, which was abrogated by lactate treatment as well as by glycolysis inhibitors. Furthermore, lactate treatment modulated glucose uptake, indicating that high levels of extracellular lactate can impair metabolic reprograming induced by proinflammatory activation. These results suggest that lactate could be a potential beneficial microbiota metabolite and may constitute an overlooked effector with modulatory properties. Centro de Investigación y Desarrollo en Criotecnología de Alimentos Instituto de Estudios Inmunológicos y Fisiopatológicos |
description |
Lactate has long been considered as a metabolic by-product of cells. Recently, this view has been changed by the observation that lactate can act as a signaling molecule and regulates critical functions of the immune system. We previously identified lactate as the component responsible for the modulation of innate immune epithelial response of fermented milk supernatants in vitro. We have also shown that lactate downregulates proinflammatory responses of macrophages and dendritic cells. So far, in vivo effects of lactate on intestinal inflammation have not been reported. We evaluated the effect of intrarectal administration of lactate in a murine model of colitis induced by 2,4,6-trinitrobenzenesulfonic acid (TNBS). The increase in lactate concentration in colon promoted protective effects against TNBS-induced colitis preventing histopathological damage, as well as bacterial translocation and rise of IL-6 levels in serum. Using intestinal epithelial reporter cells, we found that flagellin treatment induced reporter gene expression, which was abrogated by lactate treatment as well as by glycolysis inhibitors. Furthermore, lactate treatment modulated glucose uptake, indicating that high levels of extracellular lactate can impair metabolic reprograming induced by proinflammatory activation. These results suggest that lactate could be a potential beneficial microbiota metabolite and may constitute an overlooked effector with modulatory properties. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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http://sedici.unlp.edu.ar/handle/10915/86913 |
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http://sedici.unlp.edu.ar/handle/10915/86913 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
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info:eu-repo/semantics/altIdentifier/issn/1664-3224 info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2016.00651 |
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openAccess |
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http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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