Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps
- Autores
- Mugnaini, Matías; Trinchero, Mariela Fernanda; Schinder, Alejandro Fabián; Kropff, Emilio; Piatti, Veronica del Carmen
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Mammalian hippocampal circuits undergo extensive remodeling through adult neurogenesis. While this process has been widely studied, the specific contribution of adultborn granule cells (aGCs) to spatial operations in the hippocampus remains unknown. Here we show that optogenetic activation of 4-week-old (young) aGCs in free-foraging mice produces a non-reversible reconfiguration of spatial maps in proximal CA3, while rarely evoking neural activity. Stimulation of the same neuronal cohort on subsequent days recruits CA3 neurons with increased efficacy but fails to induce further remapping. In contrast, stimulation of 8-week-old (mature) aGCs can reliably activate CA3 cells but produce no alterations in spatial maps. Our results reveal a unique role of young aGCs inremodeling CA3 representations, a potential that can be depleated and is lost withmaturation. This ability could contribute to generate orthogonalized downstream codes supporting pattern separation.
Fil: Mugnaini, Matías. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Trinchero, Mariela Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Schinder, Alejandro Fabián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Kropff, Emilio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina
Fil: Piatti, Veronica del Carmen. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina - Materia
-
HIPPOCAMPUS
ADULT NEUROGENESIS
PLACE CELLS
REMAPPING
PATTERN SEPARATION
PLASTICITY
MOSSY FIBERS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/215976
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/215976 |
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CONICET Digital (CONICET) |
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Unique potential of immature adult-born neurons for the remodeling of CA3 spatial mapsMugnaini, MatíasTrinchero, Mariela FernandaSchinder, Alejandro FabiánKropff, EmilioPiatti, Veronica del CarmenHIPPOCAMPUSADULT NEUROGENESISPLACE CELLSREMAPPINGPATTERN SEPARATIONPLASTICITYMOSSY FIBERShttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1https://purl.org/becyt/ford/5.1https://purl.org/becyt/ford/5Mammalian hippocampal circuits undergo extensive remodeling through adult neurogenesis. While this process has been widely studied, the specific contribution of adultborn granule cells (aGCs) to spatial operations in the hippocampus remains unknown. Here we show that optogenetic activation of 4-week-old (young) aGCs in free-foraging mice produces a non-reversible reconfiguration of spatial maps in proximal CA3, while rarely evoking neural activity. Stimulation of the same neuronal cohort on subsequent days recruits CA3 neurons with increased efficacy but fails to induce further remapping. In contrast, stimulation of 8-week-old (mature) aGCs can reliably activate CA3 cells but produce no alterations in spatial maps. Our results reveal a unique role of young aGCs inremodeling CA3 representations, a potential that can be depleated and is lost withmaturation. This ability could contribute to generate orthogonalized downstream codes supporting pattern separation.Fil: Mugnaini, Matías. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Trinchero, Mariela Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Schinder, Alejandro Fabián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Kropff, Emilio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaFil: Piatti, Veronica del Carmen. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; ArgentinaCold Spring Harbor Laboratory Press2022-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/215976Mugnaini, Matías; Trinchero, Mariela Fernanda; Schinder, Alejandro Fabián; Kropff, Emilio; Piatti, Veronica del Carmen; Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps; Cold Spring Harbor Laboratory Press; BioRxiv; 2023; 9-2022; 1-392692-8205CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.biorxiv.org/content/10.1101/2022.09.14.507576v2info:eu-repo/semantics/altIdentifier/doi/10.1101/2022.09.14.507576info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:44:06Zoai:ri.conicet.gov.ar:11336/215976instacron: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:34982025-10-15 14:44:06.8CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps |
title |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps |
spellingShingle |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps Mugnaini, Matías HIPPOCAMPUS ADULT NEUROGENESIS PLACE CELLS REMAPPING PATTERN SEPARATION PLASTICITY MOSSY FIBERS |
title_short |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps |
title_full |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps |
title_fullStr |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps |
title_full_unstemmed |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps |
title_sort |
Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps |
dc.creator.none.fl_str_mv |
Mugnaini, Matías Trinchero, Mariela Fernanda Schinder, Alejandro Fabián Kropff, Emilio Piatti, Veronica del Carmen |
author |
Mugnaini, Matías |
author_facet |
Mugnaini, Matías Trinchero, Mariela Fernanda Schinder, Alejandro Fabián Kropff, Emilio Piatti, Veronica del Carmen |
author_role |
author |
author2 |
Trinchero, Mariela Fernanda Schinder, Alejandro Fabián Kropff, Emilio Piatti, Veronica del Carmen |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
HIPPOCAMPUS ADULT NEUROGENESIS PLACE CELLS REMAPPING PATTERN SEPARATION PLASTICITY MOSSY FIBERS |
topic |
HIPPOCAMPUS ADULT NEUROGENESIS PLACE CELLS REMAPPING PATTERN SEPARATION PLASTICITY MOSSY FIBERS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/5.1 https://purl.org/becyt/ford/5 |
dc.description.none.fl_txt_mv |
Mammalian hippocampal circuits undergo extensive remodeling through adult neurogenesis. While this process has been widely studied, the specific contribution of adultborn granule cells (aGCs) to spatial operations in the hippocampus remains unknown. Here we show that optogenetic activation of 4-week-old (young) aGCs in free-foraging mice produces a non-reversible reconfiguration of spatial maps in proximal CA3, while rarely evoking neural activity. Stimulation of the same neuronal cohort on subsequent days recruits CA3 neurons with increased efficacy but fails to induce further remapping. In contrast, stimulation of 8-week-old (mature) aGCs can reliably activate CA3 cells but produce no alterations in spatial maps. Our results reveal a unique role of young aGCs inremodeling CA3 representations, a potential that can be depleated and is lost withmaturation. This ability could contribute to generate orthogonalized downstream codes supporting pattern separation. Fil: Mugnaini, Matías. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina Fil: Trinchero, Mariela Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina Fil: Schinder, Alejandro Fabián. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina Fil: Kropff, Emilio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina Fil: Piatti, Veronica del Carmen. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina |
description |
Mammalian hippocampal circuits undergo extensive remodeling through adult neurogenesis. While this process has been widely studied, the specific contribution of adultborn granule cells (aGCs) to spatial operations in the hippocampus remains unknown. Here we show that optogenetic activation of 4-week-old (young) aGCs in free-foraging mice produces a non-reversible reconfiguration of spatial maps in proximal CA3, while rarely evoking neural activity. Stimulation of the same neuronal cohort on subsequent days recruits CA3 neurons with increased efficacy but fails to induce further remapping. In contrast, stimulation of 8-week-old (mature) aGCs can reliably activate CA3 cells but produce no alterations in spatial maps. Our results reveal a unique role of young aGCs inremodeling CA3 representations, a potential that can be depleated and is lost withmaturation. This ability could contribute to generate orthogonalized downstream codes supporting pattern separation. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09 |
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/11336/215976 Mugnaini, Matías; Trinchero, Mariela Fernanda; Schinder, Alejandro Fabián; Kropff, Emilio; Piatti, Veronica del Carmen; Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps; Cold Spring Harbor Laboratory Press; BioRxiv; 2023; 9-2022; 1-39 2692-8205 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/215976 |
identifier_str_mv |
Mugnaini, Matías; Trinchero, Mariela Fernanda; Schinder, Alejandro Fabián; Kropff, Emilio; Piatti, Veronica del Carmen; Unique potential of immature adult-born neurons for the remodeling of CA3 spatial maps; Cold Spring Harbor Laboratory Press; BioRxiv; 2023; 9-2022; 1-39 2692-8205 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://www.biorxiv.org/content/10.1101/2022.09.14.507576v2 info:eu-repo/semantics/altIdentifier/doi/10.1101/2022.09.14.507576 |
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 |
Cold Spring Harbor Laboratory Press |
publisher.none.fl_str_mv |
Cold Spring Harbor Laboratory Press |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
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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1846082949915607040 |
score |
13.22299 |