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spelling todo:paper_03043940_v434_n2_p165_Lipovsek2023-10-03T15:20:19Z Properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy Lipovsek, M. Plazas, P. Savino, J. Klaassen, A. Boulter, J. Elgoyhen, A.B. Katz, E. ACh Desensitization Epilepsy Ion channels Nicotinic receptors acetylcholine alpha4beta2 nicotinic receptor nicotinic receptor unclassified drug animal cell article autosomal dominant disorder controlled study electrophysiology focal epilepsy frontal lobe epilepsy gene insertion gene mutation heterozygosity homozygosity nonhuman nucleotide sequence priority journal receptor down regulation Xenopus Acetylcholine Animals Cholinergic Agents Epilepsies, Partial Genes, Dominant Heterozygote Homozygote Ion Channel Gating Mice Models, Chemical Mutagenesis Oocytes Patch-Clamp Techniques Receptors, Nicotinic Xenopus We characterized, by electrophysiological methods, two biophysical properties of murine recombinant α4β2 nicotinic acetylcholine receptors (nAChR) bearing a mutation (α4:+L264α4:β2 or α4:S252Fα4:β2) linked to autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE). Sensitivity to acetylcholine (ACh) was increased by the S252F substitution expressed in heterozygosis (α4:S252Fα4:β2) but was markedly reduced when this mutation was expressed in homozygosis (S252Fα4:β2). ACh sensitivity was not altered by the +L264 insertion. Moreover, receptor desensitization was significantly increased by both mutations expressed in heterozygosis. These results are in general agreement to those of rat and human recombinant receptors bearing the same mutations, thus contributing to validate the use of knock-in mice harboring ADNFLE mutations as models to study this pathology. © 2008 Elsevier Ireland Ltd. All rights reserved. Fil:Lipovsek, M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Plazas, P. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Katz, E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03043940_v434_n2_p165_Lipovsek
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic ACh
Desensitization
Epilepsy
Ion channels
Nicotinic receptors
acetylcholine
alpha4beta2 nicotinic receptor
nicotinic receptor
unclassified drug
animal cell
article
autosomal dominant disorder
controlled study
electrophysiology
focal epilepsy
frontal lobe epilepsy
gene insertion
gene mutation
heterozygosity
homozygosity
nonhuman
nucleotide sequence
priority journal
receptor down regulation
Xenopus
Acetylcholine
Animals
Cholinergic Agents
Epilepsies, Partial
Genes, Dominant
Heterozygote
Homozygote
Ion Channel Gating
Mice
Models, Chemical
Mutagenesis
Oocytes
Patch-Clamp Techniques
Receptors, Nicotinic
Xenopus
spellingShingle ACh
Desensitization
Epilepsy
Ion channels
Nicotinic receptors
acetylcholine
alpha4beta2 nicotinic receptor
nicotinic receptor
unclassified drug
animal cell
article
autosomal dominant disorder
controlled study
electrophysiology
focal epilepsy
frontal lobe epilepsy
gene insertion
gene mutation
heterozygosity
homozygosity
nonhuman
nucleotide sequence
priority journal
receptor down regulation
Xenopus
Acetylcholine
Animals
Cholinergic Agents
Epilepsies, Partial
Genes, Dominant
Heterozygote
Homozygote
Ion Channel Gating
Mice
Models, Chemical
Mutagenesis
Oocytes
Patch-Clamp Techniques
Receptors, Nicotinic
Xenopus
Lipovsek, M.
Plazas, P.
Savino, J.
Klaassen, A.
Boulter, J.
Elgoyhen, A.B.
Katz, E.
Properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy
topic_facet ACh
Desensitization
Epilepsy
Ion channels
Nicotinic receptors
acetylcholine
alpha4beta2 nicotinic receptor
nicotinic receptor
unclassified drug
animal cell
article
autosomal dominant disorder
controlled study
electrophysiology
focal epilepsy
frontal lobe epilepsy
gene insertion
gene mutation
heterozygosity
homozygosity
nonhuman
nucleotide sequence
priority journal
receptor down regulation
Xenopus
Acetylcholine
Animals
Cholinergic Agents
Epilepsies, Partial
Genes, Dominant
Heterozygote
Homozygote
Ion Channel Gating
Mice
Models, Chemical
Mutagenesis
Oocytes
Patch-Clamp Techniques
Receptors, Nicotinic
Xenopus
description We characterized, by electrophysiological methods, two biophysical properties of murine recombinant α4β2 nicotinic acetylcholine receptors (nAChR) bearing a mutation (α4:+L264α4:β2 or α4:S252Fα4:β2) linked to autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE). Sensitivity to acetylcholine (ACh) was increased by the S252F substitution expressed in heterozygosis (α4:S252Fα4:β2) but was markedly reduced when this mutation was expressed in homozygosis (S252Fα4:β2). ACh sensitivity was not altered by the +L264 insertion. Moreover, receptor desensitization was significantly increased by both mutations expressed in heterozygosis. These results are in general agreement to those of rat and human recombinant receptors bearing the same mutations, thus contributing to validate the use of knock-in mice harboring ADNFLE mutations as models to study this pathology. © 2008 Elsevier Ireland Ltd. All rights reserved.
format JOUR
author Lipovsek, M.
Plazas, P.
Savino, J.
Klaassen, A.
Boulter, J.
Elgoyhen, A.B.
Katz, E.
author_facet Lipovsek, M.
Plazas, P.
Savino, J.
Klaassen, A.
Boulter, J.
Elgoyhen, A.B.
Katz, E.
author_sort Lipovsek, M.
title Properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy
title_short Properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy
title_full Properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy
title_fullStr Properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy
title_full_unstemmed Properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy
title_sort properties of mutated murine α4β2 nicotinic receptors linked to partial epilepsy
url http://hdl.handle.net/20.500.12110/paper_03043940_v434_n2_p165_Lipovsek
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