Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb
- Autores
- Benzi Juncos, Oriana Nicole; Conde, Melisa Ailén; Alza, Natalia Paola; Salvador, Gabriela Alejandra
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- INTRODUÇÃO: Maneb is a dithiocarbamate pesticide which prolonged use is considered an environmental risk factor for Parkinson’s disease (PD). An important component in PD pathogenesis is neuroinflammation. Chronic neuroinflammation is established when resolution process fails to limit pro-inflammatory stimulus, thus triggering neuronal death. Prostaglandins and resolvins are specialized and essential lipid mediators in the inflammation/resolution process. They are oxygenated derivatives of arachidonic (AA) and docosahexaenoic (DHA) acids that act as ligands for specific G-protein coupled receptors. OBJETIVOS: Our aim was to study the spatial-temporal production of inflammation/resolution signals and their specific role throughout Maneb-induced injury in neuronal and glial cells. For this purpose, molecular components of the inflammation/resolution cascade were studied in dopaminergic neurons, astrocytes and their secretomes challenged with the pesticide. MÉTODOS: N27 dopaminergic neuronal and C6 astrocyte cell lines were exposed to 20 µM Maneb or vehicle for 24 h in the presence of pharmacological inhibitors and antagonists of different components of the inflammation/resolution pathways. Cell viability and cellular oxidant levels were determined by MTT reduction and dichlorofluorescein assays, respectively. Cell proliferation was evaluated by Bromodeoxyuridine incorporation assay. After treatments, protein and gene expression was measured by Western blot, Immunocytochemistry and RT-qPCR. AA and DHA content was assessed by GC-MS. RESULTADOS: First, we characterized the redox status of neurons exposed to Maneb. We determined that the increase in reactive oxygen species triggered by the pesticide was associated with a downregulation of antioxidant defenses (hemeoxigenase-1, glutathione cysteine ligase and superoxide dismutase). The oxidative injury triggered by Maneb was accompanied by a different profile in AA and DHA content in neurons and astrocytes. Increased neuronal DHA levels were associated with exacerbated cell death observed in the presence of Maneb and the FPR2/ALX antagonist, QuinC7. Astrocyte-derived secretome was able to prevent Maneb-triggered neuronal death and also to revert the deleterious effect of FPR2/ALX blockage. In line with this, astrocytes showed decreased AA and DHA levels, which were coincident with their secretome-mediated neuroprotective role. Pharmacological inhibition of key enzymes (cyclooxygenase-2, lipoxygenase-15, cytochrome P450) responsible for the production of inflammation/resolution related lipid mediators demonstrated that the spatial (neurons or astrocytes) activation of these pathways was involved in the cellular response to Maneb- induced toxicity. CONCLUSÕES: Our results point towards a neuroprotective role of astroglia through the orchestrated activation of resolution mechanisms against pesticide toxicity
Fil: Benzi Juncos, Oriana Nicole. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Conde, Melisa Ailén. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Alza, Natalia Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
Fil: Salvador, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina
3rd Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias Congress
Belem
Brasil
Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias - Materia
-
Maneb
neuron-glia communication - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/229919
Ver los metadatos del registro completo
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Novel insights into neuron-glia communication: the case of neuroinflammation triggered by ManebBenzi Juncos, Oriana NicoleConde, Melisa AilénAlza, Natalia PaolaSalvador, Gabriela AlejandraManebneuron-glia communicationhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1INTRODUÇÃO: Maneb is a dithiocarbamate pesticide which prolonged use is considered an environmental risk factor for Parkinson’s disease (PD). An important component in PD pathogenesis is neuroinflammation. Chronic neuroinflammation is established when resolution process fails to limit pro-inflammatory stimulus, thus triggering neuronal death. Prostaglandins and resolvins are specialized and essential lipid mediators in the inflammation/resolution process. They are oxygenated derivatives of arachidonic (AA) and docosahexaenoic (DHA) acids that act as ligands for specific G-protein coupled receptors. OBJETIVOS: Our aim was to study the spatial-temporal production of inflammation/resolution signals and their specific role throughout Maneb-induced injury in neuronal and glial cells. For this purpose, molecular components of the inflammation/resolution cascade were studied in dopaminergic neurons, astrocytes and their secretomes challenged with the pesticide. MÉTODOS: N27 dopaminergic neuronal and C6 astrocyte cell lines were exposed to 20 µM Maneb or vehicle for 24 h in the presence of pharmacological inhibitors and antagonists of different components of the inflammation/resolution pathways. Cell viability and cellular oxidant levels were determined by MTT reduction and dichlorofluorescein assays, respectively. Cell proliferation was evaluated by Bromodeoxyuridine incorporation assay. After treatments, protein and gene expression was measured by Western blot, Immunocytochemistry and RT-qPCR. AA and DHA content was assessed by GC-MS. RESULTADOS: First, we characterized the redox status of neurons exposed to Maneb. We determined that the increase in reactive oxygen species triggered by the pesticide was associated with a downregulation of antioxidant defenses (hemeoxigenase-1, glutathione cysteine ligase and superoxide dismutase). The oxidative injury triggered by Maneb was accompanied by a different profile in AA and DHA content in neurons and astrocytes. Increased neuronal DHA levels were associated with exacerbated cell death observed in the presence of Maneb and the FPR2/ALX antagonist, QuinC7. Astrocyte-derived secretome was able to prevent Maneb-triggered neuronal death and also to revert the deleterious effect of FPR2/ALX blockage. In line with this, astrocytes showed decreased AA and DHA levels, which were coincident with their secretome-mediated neuroprotective role. Pharmacological inhibition of key enzymes (cyclooxygenase-2, lipoxygenase-15, cytochrome P450) responsible for the production of inflammation/resolution related lipid mediators demonstrated that the spatial (neurons or astrocytes) activation of these pathways was involved in the cellular response to Maneb- induced toxicity. CONCLUSÕES: Our results point towards a neuroprotective role of astroglia through the orchestrated activation of resolution mechanisms against pesticide toxicityFil: Benzi Juncos, Oriana Nicole. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Conde, Melisa Ailén. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Alza, Natalia Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; ArgentinaFil: Salvador, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina3rd Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias CongressBelemBrasilFederación de Asociaciones Latinoamericanas y del Caribe de NeurocienciasFederación de Asociaciones Latinoamericanas y del Caribe de Neurociencias2022info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectCongresoBookhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/229919Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb; 3rd Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias Congress; Belem; Brasil; 2022; 397-398CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://neurocienciasfalan.org/site/falan-congress-2022-announcement/Internacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:55:11Zoai:ri.conicet.gov.ar:11336/229919instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:55:12.065CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb |
title |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb |
spellingShingle |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb Benzi Juncos, Oriana Nicole Maneb neuron-glia communication |
title_short |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb |
title_full |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb |
title_fullStr |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb |
title_full_unstemmed |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb |
title_sort |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb |
dc.creator.none.fl_str_mv |
Benzi Juncos, Oriana Nicole Conde, Melisa Ailén Alza, Natalia Paola Salvador, Gabriela Alejandra |
author |
Benzi Juncos, Oriana Nicole |
author_facet |
Benzi Juncos, Oriana Nicole Conde, Melisa Ailén Alza, Natalia Paola Salvador, Gabriela Alejandra |
author_role |
author |
author2 |
Conde, Melisa Ailén Alza, Natalia Paola Salvador, Gabriela Alejandra |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Maneb neuron-glia communication |
topic |
Maneb neuron-glia communication |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
INTRODUÇÃO: Maneb is a dithiocarbamate pesticide which prolonged use is considered an environmental risk factor for Parkinson’s disease (PD). An important component in PD pathogenesis is neuroinflammation. Chronic neuroinflammation is established when resolution process fails to limit pro-inflammatory stimulus, thus triggering neuronal death. Prostaglandins and resolvins are specialized and essential lipid mediators in the inflammation/resolution process. They are oxygenated derivatives of arachidonic (AA) and docosahexaenoic (DHA) acids that act as ligands for specific G-protein coupled receptors. OBJETIVOS: Our aim was to study the spatial-temporal production of inflammation/resolution signals and their specific role throughout Maneb-induced injury in neuronal and glial cells. For this purpose, molecular components of the inflammation/resolution cascade were studied in dopaminergic neurons, astrocytes and their secretomes challenged with the pesticide. MÉTODOS: N27 dopaminergic neuronal and C6 astrocyte cell lines were exposed to 20 µM Maneb or vehicle for 24 h in the presence of pharmacological inhibitors and antagonists of different components of the inflammation/resolution pathways. Cell viability and cellular oxidant levels were determined by MTT reduction and dichlorofluorescein assays, respectively. Cell proliferation was evaluated by Bromodeoxyuridine incorporation assay. After treatments, protein and gene expression was measured by Western blot, Immunocytochemistry and RT-qPCR. AA and DHA content was assessed by GC-MS. RESULTADOS: First, we characterized the redox status of neurons exposed to Maneb. We determined that the increase in reactive oxygen species triggered by the pesticide was associated with a downregulation of antioxidant defenses (hemeoxigenase-1, glutathione cysteine ligase and superoxide dismutase). The oxidative injury triggered by Maneb was accompanied by a different profile in AA and DHA content in neurons and astrocytes. Increased neuronal DHA levels were associated with exacerbated cell death observed in the presence of Maneb and the FPR2/ALX antagonist, QuinC7. Astrocyte-derived secretome was able to prevent Maneb-triggered neuronal death and also to revert the deleterious effect of FPR2/ALX blockage. In line with this, astrocytes showed decreased AA and DHA levels, which were coincident with their secretome-mediated neuroprotective role. Pharmacological inhibition of key enzymes (cyclooxygenase-2, lipoxygenase-15, cytochrome P450) responsible for the production of inflammation/resolution related lipid mediators demonstrated that the spatial (neurons or astrocytes) activation of these pathways was involved in the cellular response to Maneb- induced toxicity. CONCLUSÕES: Our results point towards a neuroprotective role of astroglia through the orchestrated activation of resolution mechanisms against pesticide toxicity Fil: Benzi Juncos, Oriana Nicole. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Conde, Melisa Ailén. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Alza, Natalia Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina Fil: Salvador, Gabriela Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; Argentina. Universidad Nacional del Sur. Departamento de Biología, Bioquímica y Farmacia; Argentina 3rd Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias Congress Belem Brasil Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias |
description |
INTRODUÇÃO: Maneb is a dithiocarbamate pesticide which prolonged use is considered an environmental risk factor for Parkinson’s disease (PD). An important component in PD pathogenesis is neuroinflammation. Chronic neuroinflammation is established when resolution process fails to limit pro-inflammatory stimulus, thus triggering neuronal death. Prostaglandins and resolvins are specialized and essential lipid mediators in the inflammation/resolution process. They are oxygenated derivatives of arachidonic (AA) and docosahexaenoic (DHA) acids that act as ligands for specific G-protein coupled receptors. OBJETIVOS: Our aim was to study the spatial-temporal production of inflammation/resolution signals and their specific role throughout Maneb-induced injury in neuronal and glial cells. For this purpose, molecular components of the inflammation/resolution cascade were studied in dopaminergic neurons, astrocytes and their secretomes challenged with the pesticide. MÉTODOS: N27 dopaminergic neuronal and C6 astrocyte cell lines were exposed to 20 µM Maneb or vehicle for 24 h in the presence of pharmacological inhibitors and antagonists of different components of the inflammation/resolution pathways. Cell viability and cellular oxidant levels were determined by MTT reduction and dichlorofluorescein assays, respectively. Cell proliferation was evaluated by Bromodeoxyuridine incorporation assay. After treatments, protein and gene expression was measured by Western blot, Immunocytochemistry and RT-qPCR. AA and DHA content was assessed by GC-MS. RESULTADOS: First, we characterized the redox status of neurons exposed to Maneb. We determined that the increase in reactive oxygen species triggered by the pesticide was associated with a downregulation of antioxidant defenses (hemeoxigenase-1, glutathione cysteine ligase and superoxide dismutase). The oxidative injury triggered by Maneb was accompanied by a different profile in AA and DHA content in neurons and astrocytes. Increased neuronal DHA levels were associated with exacerbated cell death observed in the presence of Maneb and the FPR2/ALX antagonist, QuinC7. Astrocyte-derived secretome was able to prevent Maneb-triggered neuronal death and also to revert the deleterious effect of FPR2/ALX blockage. In line with this, astrocytes showed decreased AA and DHA levels, which were coincident with their secretome-mediated neuroprotective role. Pharmacological inhibition of key enzymes (cyclooxygenase-2, lipoxygenase-15, cytochrome P450) responsible for the production of inflammation/resolution related lipid mediators demonstrated that the spatial (neurons or astrocytes) activation of these pathways was involved in the cellular response to Maneb- induced toxicity. CONCLUSÕES: Our results point towards a neuroprotective role of astroglia through the orchestrated activation of resolution mechanisms against pesticide toxicity |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/conferenceObject Congreso Book http://purl.org/coar/resource_type/c_5794 info:ar-repo/semantics/documentoDeConferencia |
status_str |
publishedVersion |
format |
conferenceObject |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/229919 Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb; 3rd Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias Congress; Belem; Brasil; 2022; 397-398 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/229919 |
identifier_str_mv |
Novel insights into neuron-glia communication: the case of neuroinflammation triggered by Maneb; 3rd Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias Congress; Belem; Brasil; 2022; 397-398 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://neurocienciasfalan.org/site/falan-congress-2022-announcement/ |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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application/pdf application/pdf application/pdf application/pdf application/pdf |
dc.coverage.none.fl_str_mv |
Internacional |
dc.publisher.none.fl_str_mv |
Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias |
publisher.none.fl_str_mv |
Federación de Asociaciones Latinoamericanas y del Caribe de Neurociencias |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.13397 |