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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/69397
Ver los metadatos del registro completo
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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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score |
13.13397 |