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
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/86913

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network_name_str SEDICI (UNLP)
spelling 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
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/86913
url http://sedici.unlp.edu.ar/handle/10915/86913
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/1664-3224
info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2016.00651
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
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instname_str Universidad Nacional de La Plata
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repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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