proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons

Autores
Gibon, Julien; Buckley, Shannon M.; Unsain, Nicolas; Kaartinen, Vesa; Séguéla, Philippe; Barker, Philip A.
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Persistent firing of entorhinal cortex (EC) pyramidal neurons is a key component of working and spatial memory. We report here that a pro-brain-derived neurotrophic factor (proBDNF)-dependent p75NTR signaling pathway plays a major role in excitability and persistent activity of pyramidal neurons in layer V of the EC. Using electrophysiological recordings, we show that proBDNF suppresses persistent firing in entorhinal slices from wild-type mice but not from p75NTR-null mice. Conversely, function-blocking proBDNF antibodies enhance excitability of pyramidal neurons and facilitate their persistent firing, and acute exposure to function-blocking p75NTR antibodies results in enhanced firing activity of pyramidal neurons. Genetic deletion of p75NTR specifically in neurons or during adulthood also induces enhanced excitability and persistent activity, indicating that the proBDNF-p75NTR signaling cascade functions within adult neurons to inhibit pyramidal activity. Phosphatidylinositol 4,5-bisphosphate (PIP2)-sensitive transient receptor potential canonical channels play a critical role in mediating persistent firing in the EC and we hypothesized that proBDNF-dependent p75NTR activation regulates PIP2 levels. Accordingly, proBDNF decreases cholinergic calcium responses in cortical neurons and affects carbachol-induced depletion of PIP2. Further, we show that the modulation of persistent firing by proBDNF relies on a p75NTR-Rac1-PI4K pathway. The hypothesis that proBDNF and p75NTR maintain network homeostasis in the adult CNS was tested in vivo and we report that p75NTR-null mice show improvements in working memory but also display an increased propensity for severe seizures. We propose that the proBDNF-p75NTR axis controls pyramidal neuron excitability and persistent activity to balance EC performance with the risk of runaway activity.
Fil: Gibon, Julien. McGill University; Canadá
Fil: Buckley, Shannon M.. McGill University; Canadá
Fil: Unsain, Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. McGill University; Canadá
Fil: Kaartinen, Vesa. University of Michigan; Estados Unidos
Fil: Séguéla, Philippe. McGill University; Canadá
Fil: Barker, Philip A.. McGill University; Canadá
Materia
ENTORHINAL CORTEX
EPILEPSY
P75NTR
PERSISTENT FIRING
PROBDNF
WORKING MEMORY
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/69397

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oai_identifier_str oai:ri.conicet.gov.ar:11336/69397
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neuronsGibon, JulienBuckley, Shannon M.Unsain, NicolasKaartinen, VesaSéguéla, PhilippeBarker, Philip A.ENTORHINAL CORTEXEPILEPSYP75NTRPERSISTENT FIRINGPROBDNFWORKING MEMORYhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Persistent firing of entorhinal cortex (EC) pyramidal neurons is a key component of working and spatial memory. We report here that a pro-brain-derived neurotrophic factor (proBDNF)-dependent p75NTR signaling pathway plays a major role in excitability and persistent activity of pyramidal neurons in layer V of the EC. Using electrophysiological recordings, we show that proBDNF suppresses persistent firing in entorhinal slices from wild-type mice but not from p75NTR-null mice. Conversely, function-blocking proBDNF antibodies enhance excitability of pyramidal neurons and facilitate their persistent firing, and acute exposure to function-blocking p75NTR antibodies results in enhanced firing activity of pyramidal neurons. Genetic deletion of p75NTR specifically in neurons or during adulthood also induces enhanced excitability and persistent activity, indicating that the proBDNF-p75NTR signaling cascade functions within adult neurons to inhibit pyramidal activity. Phosphatidylinositol 4,5-bisphosphate (PIP2)-sensitive transient receptor potential canonical channels play a critical role in mediating persistent firing in the EC and we hypothesized that proBDNF-dependent p75NTR activation regulates PIP2 levels. Accordingly, proBDNF decreases cholinergic calcium responses in cortical neurons and affects carbachol-induced depletion of PIP2. Further, we show that the modulation of persistent firing by proBDNF relies on a p75NTR-Rac1-PI4K pathway. The hypothesis that proBDNF and p75NTR maintain network homeostasis in the adult CNS was tested in vivo and we report that p75NTR-null mice show improvements in working memory but also display an increased propensity for severe seizures. We propose that the proBDNF-p75NTR axis controls pyramidal neuron excitability and persistent activity to balance EC performance with the risk of runaway activity.Fil: Gibon, Julien. McGill University; CanadáFil: Buckley, Shannon M.. McGill University; CanadáFil: Unsain, Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. McGill University; CanadáFil: Kaartinen, Vesa. University of Michigan; Estados UnidosFil: Séguéla, Philippe. McGill University; CanadáFil: Barker, Philip A.. McGill University; CanadáSociety for Neuroscience2015-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/69397Gibon, Julien; Buckley, Shannon M.; Unsain, Nicolas; Kaartinen, Vesa; Séguéla, Philippe; et al.; proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons; Society for Neuroscience; Journal of Neuroscience; 35; 26; 7-2015; 9741-97530270-6474CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1523/JNEUROSCI.4655-14.2015info:eu-repo/semantics/altIdentifier/url/http://www.jneurosci.org/content/35/26/9741info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:50:35Zoai:ri.conicet.gov.ar:11336/69397instacron: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 09:50:35.797CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
title proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
spellingShingle proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
Gibon, Julien
ENTORHINAL CORTEX
EPILEPSY
P75NTR
PERSISTENT FIRING
PROBDNF
WORKING MEMORY
title_short proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
title_full proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
title_fullStr proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
title_full_unstemmed proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
title_sort proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons
dc.creator.none.fl_str_mv Gibon, Julien
Buckley, Shannon M.
Unsain, Nicolas
Kaartinen, Vesa
Séguéla, Philippe
Barker, Philip A.
author Gibon, Julien
author_facet Gibon, Julien
Buckley, Shannon M.
Unsain, Nicolas
Kaartinen, Vesa
Séguéla, Philippe
Barker, Philip A.
author_role author
author2 Buckley, Shannon M.
Unsain, Nicolas
Kaartinen, Vesa
Séguéla, Philippe
Barker, Philip A.
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv ENTORHINAL CORTEX
EPILEPSY
P75NTR
PERSISTENT FIRING
PROBDNF
WORKING MEMORY
topic ENTORHINAL CORTEX
EPILEPSY
P75NTR
PERSISTENT FIRING
PROBDNF
WORKING MEMORY
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Persistent firing of entorhinal cortex (EC) pyramidal neurons is a key component of working and spatial memory. We report here that a pro-brain-derived neurotrophic factor (proBDNF)-dependent p75NTR signaling pathway plays a major role in excitability and persistent activity of pyramidal neurons in layer V of the EC. Using electrophysiological recordings, we show that proBDNF suppresses persistent firing in entorhinal slices from wild-type mice but not from p75NTR-null mice. Conversely, function-blocking proBDNF antibodies enhance excitability of pyramidal neurons and facilitate their persistent firing, and acute exposure to function-blocking p75NTR antibodies results in enhanced firing activity of pyramidal neurons. Genetic deletion of p75NTR specifically in neurons or during adulthood also induces enhanced excitability and persistent activity, indicating that the proBDNF-p75NTR signaling cascade functions within adult neurons to inhibit pyramidal activity. Phosphatidylinositol 4,5-bisphosphate (PIP2)-sensitive transient receptor potential canonical channels play a critical role in mediating persistent firing in the EC and we hypothesized that proBDNF-dependent p75NTR activation regulates PIP2 levels. Accordingly, proBDNF decreases cholinergic calcium responses in cortical neurons and affects carbachol-induced depletion of PIP2. Further, we show that the modulation of persistent firing by proBDNF relies on a p75NTR-Rac1-PI4K pathway. The hypothesis that proBDNF and p75NTR maintain network homeostasis in the adult CNS was tested in vivo and we report that p75NTR-null mice show improvements in working memory but also display an increased propensity for severe seizures. We propose that the proBDNF-p75NTR axis controls pyramidal neuron excitability and persistent activity to balance EC performance with the risk of runaway activity.
Fil: Gibon, Julien. McGill University; Canadá
Fil: Buckley, Shannon M.. McGill University; Canadá
Fil: Unsain, Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. McGill University; Canadá
Fil: Kaartinen, Vesa. University of Michigan; Estados Unidos
Fil: Séguéla, Philippe. McGill University; Canadá
Fil: Barker, Philip A.. McGill University; Canadá
description Persistent firing of entorhinal cortex (EC) pyramidal neurons is a key component of working and spatial memory. We report here that a pro-brain-derived neurotrophic factor (proBDNF)-dependent p75NTR signaling pathway plays a major role in excitability and persistent activity of pyramidal neurons in layer V of the EC. Using electrophysiological recordings, we show that proBDNF suppresses persistent firing in entorhinal slices from wild-type mice but not from p75NTR-null mice. Conversely, function-blocking proBDNF antibodies enhance excitability of pyramidal neurons and facilitate their persistent firing, and acute exposure to function-blocking p75NTR antibodies results in enhanced firing activity of pyramidal neurons. Genetic deletion of p75NTR specifically in neurons or during adulthood also induces enhanced excitability and persistent activity, indicating that the proBDNF-p75NTR signaling cascade functions within adult neurons to inhibit pyramidal activity. Phosphatidylinositol 4,5-bisphosphate (PIP2)-sensitive transient receptor potential canonical channels play a critical role in mediating persistent firing in the EC and we hypothesized that proBDNF-dependent p75NTR activation regulates PIP2 levels. Accordingly, proBDNF decreases cholinergic calcium responses in cortical neurons and affects carbachol-induced depletion of PIP2. Further, we show that the modulation of persistent firing by proBDNF relies on a p75NTR-Rac1-PI4K pathway. The hypothesis that proBDNF and p75NTR maintain network homeostasis in the adult CNS was tested in vivo and we report that p75NTR-null mice show improvements in working memory but also display an increased propensity for severe seizures. We propose that the proBDNF-p75NTR axis controls pyramidal neuron excitability and persistent activity to balance EC performance with the risk of runaway activity.
publishDate 2015
dc.date.none.fl_str_mv 2015-07
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/11336/69397
Gibon, Julien; Buckley, Shannon M.; Unsain, Nicolas; Kaartinen, Vesa; Séguéla, Philippe; et al.; proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons; Society for Neuroscience; Journal of Neuroscience; 35; 26; 7-2015; 9741-9753
0270-6474
CONICET Digital
CONICET
url http://hdl.handle.net/11336/69397
identifier_str_mv Gibon, Julien; Buckley, Shannon M.; Unsain, Nicolas; Kaartinen, Vesa; Séguéla, Philippe; et al.; proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons; Society for Neuroscience; Journal of Neuroscience; 35; 26; 7-2015; 9741-9753
0270-6474
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1523/JNEUROSCI.4655-14.2015
info:eu-repo/semantics/altIdentifier/url/http://www.jneurosci.org/content/35/26/9741
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Society for Neuroscience
publisher.none.fl_str_mv Society for Neuroscience
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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