Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein

Neuronal connectivity and synaptic remodeling are fundamental substrates for higher brain functions. Understanding their dynamics in the mammalian allocortex emerges as a critical step to tackle the cellular basis of cognitive decline that occurs during normal aging and in neurodegenerative disorder...

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Autores: Morgenstern, Nicolás Andrés, Giacomini, Damiana Paula, Lombardi, Maria Gabriela, Castaño, Eduardo Miguel, Schinder, Alejandro Fabian
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2013
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/8359
Acceso en línea:http://hdl.handle.net/11336/8359
Access Level:acceso abierto
Palabra clave:Dentate Granule Cells
Amyloid Precursor Protein
neurogenesis
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
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dc.title.none.fl_str_mv Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
title Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
spellingShingle Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
Morgenstern, Nicolás Andrés
Dentate Granule Cells
Amyloid Precursor Protein
neurogenesis
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
title_short Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
title_full Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
title_fullStr Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
title_full_unstemmed Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
title_sort Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein
dc.creator.none.fl_str_mv Morgenstern, Nicolás Andrés
Giacomini, Damiana Paula
Lombardi, Maria Gabriela
Castaño, Eduardo Miguel
Schinder, Alejandro Fabian
author Morgenstern, Nicolás Andrés
author_facet Morgenstern, Nicolás Andrés
Giacomini, Damiana Paula
Lombardi, Maria Gabriela
Castaño, Eduardo Miguel
Schinder, Alejandro Fabian
author_role author
author2 Giacomini, Damiana Paula
Lombardi, Maria Gabriela
Castaño, Eduardo Miguel
Schinder, Alejandro Fabian
author2_role author
author
author
author
dc.subject.none.fl_str_mv Dentate Granule Cells
Amyloid Precursor Protein
neurogenesis
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
topic Dentate Granule Cells
Amyloid Precursor Protein
neurogenesis
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
description Neuronal connectivity and synaptic remodeling are fundamental substrates for higher brain functions. Understanding their dynamics in the mammalian allocortex emerges as a critical step to tackle the cellular basis of cognitive decline that occurs during normal aging and in neurodegenerative disorders. In this work we have designed a novel approach to assess alterations in the dynamics of functional and structural connectivity elicited by chronic cell-autonomous overexpression of the human amyloid precursor protein (hAPP). We have taken advantage of the fact that the hippocampus continuously generates new dentate granule cells (GCs) to probe morphofunctional development of GCs expressing different variants of hAPP in a healthy background. hAPP was expressed together with a fluorescent reporter in neural progenitor cells of the dentate gyrus of juvenile mice by retroviral delivery. Neuronal progeny was analyzed several days post infection (dpi). Amyloidogenic cleavage products of hAPP such as the â-C terminal fragment (â-CTF) induced a substantial reduction in glutamatergic connectivity at 21 dpi, at which time new GCs undergo active growth and synaptogenesis. Interestingly, this effect was transient, since the strength of glutamatergic inputs was normal by 35 dpi. This delay in glutamatergic synaptogenesis was paralleled by a decrease in dendritic length with no changes in spine density, consistent with a protracted dendritic development without alterations in synapse formation. Finally, similar defects in newborn GC development were observed by overexpression of á-CTF, a non-amyloidogenic cleavage product of hAPP. These results indicate that hAPP can elicit protracted dendritic development independently of the amyloidogenic processing pathway.
publishDate 2013
dc.date.none.fl_str_mv 2013-07-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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://hdl.handle.net/11336/8359
Morgenstern, Nicolás Andrés; Giacomini, Damiana Paula; Lombardi, Maria Gabriela; Castaño, Eduardo Miguel; Schinder, Alejandro Fabian; Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein; Elsevier; Molecular And Cellular Neurosciences.; 56; 11-7-2013; 298–306
1044-7431
url http://hdl.handle.net/11336/8359
identifier_str_mv Morgenstern, Nicolás Andrés; Giacomini, Damiana Paula; Lombardi, Maria Gabriela; Castaño, Eduardo Miguel; Schinder, Alejandro Fabian; Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein; Elsevier; Molecular And Cellular Neurosciences.; 56; 11-7-2013; 298–306
1044-7431
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1044743113000699
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.mcn.2013.07.003
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791211/
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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spelling Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor ProteinMorgenstern, Nicolás AndrésGiacomini, Damiana PaulaLombardi, Maria GabrielaCastaño, Eduardo MiguelSchinder, Alejandro FabianDentate Granule CellsAmyloid Precursor Proteinneurogenesishttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Neuronal connectivity and synaptic remodeling are fundamental substrates for higher brain functions. Understanding their dynamics in the mammalian allocortex emerges as a critical step to tackle the cellular basis of cognitive decline that occurs during normal aging and in neurodegenerative disorders. In this work we have designed a novel approach to assess alterations in the dynamics of functional and structural connectivity elicited by chronic cell-autonomous overexpression of the human amyloid precursor protein (hAPP). We have taken advantage of the fact that the hippocampus continuously generates new dentate granule cells (GCs) to probe morphofunctional development of GCs expressing different variants of hAPP in a healthy background. hAPP was expressed together with a fluorescent reporter in neural progenitor cells of the dentate gyrus of juvenile mice by retroviral delivery. Neuronal progeny was analyzed several days post infection (dpi). Amyloidogenic cleavage products of hAPP such as the â-C terminal fragment (â-CTF) induced a substantial reduction in glutamatergic connectivity at 21 dpi, at which time new GCs undergo active growth and synaptogenesis. Interestingly, this effect was transient, since the strength of glutamatergic inputs was normal by 35 dpi. This delay in glutamatergic synaptogenesis was paralleled by a decrease in dendritic length with no changes in spine density, consistent with a protracted dendritic development without alterations in synapse formation. Finally, similar defects in newborn GC development were observed by overexpression of á-CTF, a non-amyloidogenic cleavage product of hAPP. These results indicate that hAPP can elicit protracted dendritic development independently of the amyloidogenic processing pathway.Fil: Morgenstern, Nicolás Andrés. Fundación Instituto Leloir; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquimicas de Buenos Aires; ArgentinaFil: Giacomini, Damiana Paula. Fundación Instituto Leloir; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquimicas de Buenos Aires; ArgentinaFil: Lombardi, Maria Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Centro de Estudios Farmacológicos y Botánicos; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquimicas de Buenos Aires; ArgentinaFil: Castaño, Eduardo Miguel. Fundación Instituto Leloir; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquimicas de Buenos Aires; ArgentinaFil: Schinder, Alejandro Fabian. Fundación Instituto Leloir; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquimicas de Buenos Aires; ArgentinaElsevier2013-07-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/8359Morgenstern, Nicolás Andrés; Giacomini, Damiana Paula; Lombardi, Maria Gabriela; Castaño, Eduardo Miguel; Schinder, Alejandro Fabian; Delayed Dendritic Development of Newly Generated Dentate Granule Cells by Cell-Autonomous Expression of the Amyloid Precursor Protein; Elsevier; Molecular And Cellular Neurosciences.; 56; 11-7-2013; 298–3061044-7431enginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1044743113000699info:eu-repo/semantics/altIdentifier/doi/10.1016/j.mcn.2013.07.003info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791211/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2024-05-08T14:00:52Zoai:ri.conicet.gov.ar:11336/8359instacron: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:34982024-05-08 14:00:52.766CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
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