Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration

ABSTRACT: Evidence suggests that extracellular vesicles (EVs) act as mediators and biomarkers of neurodegenerative diseases. Two distinct forms of Alzheimer disease (AD) are known: a late-onset sporadic form (SAD) and an early-onset familial form (FAD). Recently, neurovascular dysfunction and altere...

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Autores:
Aguillón Niño, David Fernando
Villar Vesga, Juan Manuel
Henao Restrepo, Julián Andrés
Posada Duque, Rafael Andrés
Villegas Lanau, Carlos Andrés
Castaño Monsalve, Diana María
Arias Londoño, Julián David
Cardona Gómez, Gloria Patricia
Voshart, Daniëlle C.
Ribovski, Laís
Barazzuol, Lara
Zuhorn, Inge S.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2020
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/43063
Acceso en línea:
https://hdl.handle.net/10495/43063
Palabra clave:
Enfermedad de Alzheimer
Alzheimer Disease
Endotelio
Endothelium
Vesículas Extracelulares
Extracellular Vesicles
Organoides
Organoids
Leucocitos
Leukocytes
Plaquetas
Blood Platelets
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D004727
https://id.nlm.nih.gov/mesh/D000067128
https://id.nlm.nih.gov/mesh/D009940
https://id.nlm.nih.gov/mesh/D007962
https://id.nlm.nih.gov/mesh/D001792
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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repository_id_str
dc.title.spa.fl_str_mv Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
title Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
spellingShingle Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
Enfermedad de Alzheimer
Alzheimer Disease
Endotelio
Endothelium
Vesículas Extracelulares
Extracellular Vesicles
Organoides
Organoids
Leucocitos
Leukocytes
Plaquetas
Blood Platelets
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D004727
https://id.nlm.nih.gov/mesh/D000067128
https://id.nlm.nih.gov/mesh/D009940
https://id.nlm.nih.gov/mesh/D007962
https://id.nlm.nih.gov/mesh/D001792
title_short Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
title_full Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
title_fullStr Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
title_full_unstemmed Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
title_sort Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration
dc.creator.fl_str_mv Aguillón Niño, David Fernando
Villar Vesga, Juan Manuel
Henao Restrepo, Julián Andrés
Posada Duque, Rafael Andrés
Villegas Lanau, Carlos Andrés
Castaño Monsalve, Diana María
Arias Londoño, Julián David
Cardona Gómez, Gloria Patricia
Voshart, Daniëlle C.
Ribovski, Laís
Barazzuol, Lara
Zuhorn, Inge S.
dc.contributor.author.none.fl_str_mv Aguillón Niño, David Fernando
Villar Vesga, Juan Manuel
Henao Restrepo, Julián Andrés
Posada Duque, Rafael Andrés
Villegas Lanau, Carlos Andrés
Castaño Monsalve, Diana María
Arias Londoño, Julián David
Cardona Gómez, Gloria Patricia
Voshart, Daniëlle C.
Ribovski, Laís
Barazzuol, Lara
Zuhorn, Inge S.
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Inmunología Celular e Inmunogenética
Grupo de Neurociencias de Antioquia
Grupo Neuropsicología y Conducta
Intelligent Information Systems Lab.
dc.subject.decs.none.fl_str_mv Enfermedad de Alzheimer
Alzheimer Disease
Endotelio
Endothelium
Vesículas Extracelulares
Extracellular Vesicles
Organoides
Organoids
Leucocitos
Leukocytes
Plaquetas
Blood Platelets
topic Enfermedad de Alzheimer
Alzheimer Disease
Endotelio
Endothelium
Vesículas Extracelulares
Extracellular Vesicles
Organoides
Organoids
Leucocitos
Leukocytes
Plaquetas
Blood Platelets
https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D004727
https://id.nlm.nih.gov/mesh/D000067128
https://id.nlm.nih.gov/mesh/D009940
https://id.nlm.nih.gov/mesh/D007962
https://id.nlm.nih.gov/mesh/D001792
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000544
https://id.nlm.nih.gov/mesh/D004727
https://id.nlm.nih.gov/mesh/D000067128
https://id.nlm.nih.gov/mesh/D009940
https://id.nlm.nih.gov/mesh/D007962
https://id.nlm.nih.gov/mesh/D001792
description ABSTRACT: Evidence suggests that extracellular vesicles (EVs) act as mediators and biomarkers of neurodegenerative diseases. Two distinct forms of Alzheimer disease (AD) are known: a late-onset sporadic form (SAD) and an early-onset familial form (FAD). Recently, neurovascular dysfunction and altered systemic immunological components have been linked to AD neurodegeneration. Therefore, we characterized systemic-EVs from postmortem SAD and FAD patients and evaluated their effects on neuroglial and endothelial cells. We found increase CLN-5 spots with vesicular morphology in the abluminal portion of vessels from SAD patients. Both forms of AD were associated with larger and more numerous systemic EVs. Specifically, SAD patients showed an increase in endothelial- and leukocyte-derived EVs containing mitochondria; in contrast, FAD patients showed an increase in platelet-derived EVs. We detected a differential protein composition for SAD- and FAD-EVs associated with the coagulation cascade, inflammation, and lipid-carbohydrate metabolism. Using mono- and cocultures (endothelium-astrocytes-neurons) and human cortical organoids, we showed that AD-EVs induced cytotoxicity. Both forms of AD featured decreased neuronal branches area and astrocytic hyperreactivity, but SAD-EVs led to greater endothelial detrimental effects than FAD-EVs. In addition, FAD- and SAD-EVs affected calcium dynamics in a cortical organoid model. Our findings indicate that the phenotype of systemic AD-EVs is differentially defined by the etiopathology of the disease (SAD or FAD), which results in a differential alteration of the NVU cells implied in neurodegeneration.
publishDate 2020
dc.date.issued.none.fl_str_mv 2020
dc.date.accessioned.none.fl_str_mv 2024-11-02T23:34:04Z
dc.date.available.none.fl_str_mv 2024-11-02T23:34:04Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.citation.spa.fl_str_mv Villar-Vesga J, Henao-Restrepo J, Voshart DC, Aguillon D, Villegas A, Castaño D, Arias-Londoño JD, Zuhorn IS, Ribovski L, Barazzuol L, Cardona-Gómez GP, Posada-Duque R. Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration. Front Aging Neurosci. 2020 Nov 11;12:587989. doi: 10.3389/fnagi.2020.587989.
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/43063
dc.identifier.doi.none.fl_str_mv 10.3389/fnagi.2020.587989
dc.identifier.eissn.none.fl_str_mv 1663-4365
identifier_str_mv Villar-Vesga J, Henao-Restrepo J, Voshart DC, Aguillon D, Villegas A, Castaño D, Arias-Londoño JD, Zuhorn IS, Ribovski L, Barazzuol L, Cardona-Gómez GP, Posada-Duque R. Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration. Front Aging Neurosci. 2020 Nov 11;12:587989. doi: 10.3389/fnagi.2020.587989.
10.3389/fnagi.2020.587989
1663-4365
url https://hdl.handle.net/10495/43063
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Front. Aging. Neurosci.
dc.relation.citationendpage.spa.fl_str_mv 22
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 12
dc.relation.ispartofjournal.spa.fl_str_mv Frontiers in Aging Neuroscience
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dc.format.extent.spa.fl_str_mv 22 páginas
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spelling Aguillón Niño, David FernandoVillar Vesga, Juan ManuelHenao Restrepo, Julián AndrésPosada Duque, Rafael AndrésVillegas Lanau, Carlos AndrésCastaño Monsalve, Diana MaríaArias Londoño, Julián DavidCardona Gómez, Gloria PatriciaVoshart, Daniëlle C.Ribovski, LaísBarazzuol, LaraZuhorn, Inge S.Grupo de Inmunología Celular e InmunogenéticaGrupo de Neurociencias de AntioquiaGrupo Neuropsicología y ConductaIntelligent Information Systems Lab.2024-11-02T23:34:04Z2024-11-02T23:34:04Z2020Villar-Vesga J, Henao-Restrepo J, Voshart DC, Aguillon D, Villegas A, Castaño D, Arias-Londoño JD, Zuhorn IS, Ribovski L, Barazzuol L, Cardona-Gómez GP, Posada-Duque R. Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell Degeneration. Front Aging Neurosci. 2020 Nov 11;12:587989. doi: 10.3389/fnagi.2020.587989.https://hdl.handle.net/10495/4306310.3389/fnagi.2020.5879891663-4365ABSTRACT: Evidence suggests that extracellular vesicles (EVs) act as mediators and biomarkers of neurodegenerative diseases. Two distinct forms of Alzheimer disease (AD) are known: a late-onset sporadic form (SAD) and an early-onset familial form (FAD). Recently, neurovascular dysfunction and altered systemic immunological components have been linked to AD neurodegeneration. Therefore, we characterized systemic-EVs from postmortem SAD and FAD patients and evaluated their effects on neuroglial and endothelial cells. We found increase CLN-5 spots with vesicular morphology in the abluminal portion of vessels from SAD patients. Both forms of AD were associated with larger and more numerous systemic EVs. Specifically, SAD patients showed an increase in endothelial- and leukocyte-derived EVs containing mitochondria; in contrast, FAD patients showed an increase in platelet-derived EVs. We detected a differential protein composition for SAD- and FAD-EVs associated with the coagulation cascade, inflammation, and lipid-carbohydrate metabolism. Using mono- and cocultures (endothelium-astrocytes-neurons) and human cortical organoids, we showed that AD-EVs induced cytotoxicity. Both forms of AD featured decreased neuronal branches area and astrocytic hyperreactivity, but SAD-EVs led to greater endothelial detrimental effects than FAD-EVs. In addition, FAD- and SAD-EVs affected calcium dynamics in a cortical organoid model. Our findings indicate that the phenotype of systemic AD-EVs is differentially defined by the etiopathology of the disease (SAD or FAD), which results in a differential alteration of the NVU cells implied in neurodegeneration.Colombia. Ministerio de Ciencia, Tecnología e Innovación - MinCienciasCOL0008639COL0010744COL0007551COL002593422 páginasapplication/pdfengFrontiers MediaLausana, Suizahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer's Disease Leads to Neuroglial and Endothelial Cell DegenerationArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionEnfermedad de AlzheimerAlzheimer DiseaseEndotelioEndotheliumVesículas ExtracelularesExtracellular VesiclesOrganoidesOrganoidsLeucocitosLeukocytesPlaquetasBlood Plateletshttps://id.nlm.nih.gov/mesh/D000544https://id.nlm.nih.gov/mesh/D004727https://id.nlm.nih.gov/mesh/D000067128https://id.nlm.nih.gov/mesh/D009940https://id.nlm.nih.gov/mesh/D007962https://id.nlm.nih.gov/mesh/D001792Front. Aging. 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