Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction

Detalhes bibliográficos
Autor(a) principal: Paiva, Daisylea de Souza [UNIFESP]
Data de Publicação: 2017
Outros Autores: Alves Romariz, Simone Amaro [UNIFESP], Valente, Maria Fernanda [UNIFESP], Moraes, Luiz Bruno [UNIFESP], Covolan, Luciene [UNIFESP], Calcagnotto, Maria Elisa, Longo, Beatriz Monteiro [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://repositorio.unifesp.br/handle/11600/54560
http://dx.doi.org/10.1016/j.yebeh.2017.03.015
Resumo: Medial ganglionic eminence (MGE) is one of the sources of inhibitory interneurons during development. Following transplantation in postnatal developing brain, MGE cells can increase local inhibition suggesting a possible protection to GABAergic dysfunction in brain disorders, such as epilepsy. Since it has been shown that MGE-derived cells harvested as neurospheres are able to suppress seizures, it might be important to investigate whether these protective effects would change in different seizure models. Here, we used pentylenetetrazole(PTZ) and maximal electroshock (MES)-induced seizure models to test whether the transplantation of MGE cells would increase the threshold to trigger acute seizures. When transplanted into the neocortex (layers 3-4) of neonatal mice (postnatal days 3-4), MGE cells were able to survive and were mainly found in piriform cortex, fimbria, and ventricular wall regions. Additionally, the number of GFP + cells found in the brains of mice induced with PTZ and MES differed significantly and suggests proliferation and larger survival rate of MGE-transplanted cells after PTZ, but not MES-induced seizures. Following transplantation, there was a reduction in the number of animals presenting mild and severe seizures induced by PTZ. Furthermore, MGE-cell transplantation was able to increase threshold to seizures induced by PTZ, but was not able to prevent seizure spread induced by MES. (C) 2017 Elsevier Inc. All rights reserved.
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spelling Paiva, Daisylea de Souza [UNIFESP]Alves Romariz, Simone Amaro [UNIFESP]Valente, Maria Fernanda [UNIFESP]Moraes, Luiz Bruno [UNIFESP]Covolan, Luciene [UNIFESP]Calcagnotto, Maria ElisaLongo, Beatriz Monteiro [UNIFESP]2020-07-13T11:53:21Z2020-07-13T11:53:21Z2017Epilepsy & Behavior. San Diego, v. 70, p. 125-130, 2017.1525-5050https://repositorio.unifesp.br/handle/11600/54560http://dx.doi.org/10.1016/j.yebeh.2017.03.01510.1016/j.yebeh.2017.03.015WOS:000402447700020Medial ganglionic eminence (MGE) is one of the sources of inhibitory interneurons during development. Following transplantation in postnatal developing brain, MGE cells can increase local inhibition suggesting a possible protection to GABAergic dysfunction in brain disorders, such as epilepsy. Since it has been shown that MGE-derived cells harvested as neurospheres are able to suppress seizures, it might be important to investigate whether these protective effects would change in different seizure models. Here, we used pentylenetetrazole(PTZ) and maximal electroshock (MES)-induced seizure models to test whether the transplantation of MGE cells would increase the threshold to trigger acute seizures. When transplanted into the neocortex (layers 3-4) of neonatal mice (postnatal days 3-4), MGE cells were able to survive and were mainly found in piriform cortex, fimbria, and ventricular wall regions. Additionally, the number of GFP + cells found in the brains of mice induced with PTZ and MES differed significantly and suggests proliferation and larger survival rate of MGE-transplanted cells after PTZ, but not MES-induced seizures. Following transplantation, there was a reduction in the number of animals presenting mild and severe seizures induced by PTZ. Furthermore, MGE-cell transplantation was able to increase threshold to seizures induced by PTZ, but was not able to prevent seizure spread induced by MES. (C) 2017 Elsevier Inc. All rights reserved.FAPESPCNPqUniv Fed Sao Paulo UNIFESP, Lab Neurofisiol, Sao Paulo, BrazilUniv Fed Rio Grande do Sul, Porto Alegre, RS, BrazilUniv Fed Sao Paulo UNIFESP, Lab Neurofisiol, Sao Paulo, BrazilWeb of Science125-130engAcademic Press Inc Elsevier ScienceEpilepsy & BehaviorPentylenetetrazoleMaximal electroshockNeurosphereMedial ganglionic eminenceAcute seizureTransplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure inductioninfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleSan Diego70info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/545602021-10-05 22:05:35.846metadata only accessoai:repositorio.unifesp.br:11600/54560Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:07:45.903858Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
title Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
spellingShingle Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
Paiva, Daisylea de Souza [UNIFESP]
Pentylenetetrazole
Maximal electroshock
Neurosphere
Medial ganglionic eminence
Acute seizure
title_short Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
title_full Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
title_fullStr Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
title_full_unstemmed Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
title_sort Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
author Paiva, Daisylea de Souza [UNIFESP]
author_facet Paiva, Daisylea de Souza [UNIFESP]
Alves Romariz, Simone Amaro [UNIFESP]
Valente, Maria Fernanda [UNIFESP]
Moraes, Luiz Bruno [UNIFESP]
Covolan, Luciene [UNIFESP]
Calcagnotto, Maria Elisa
Longo, Beatriz Monteiro [UNIFESP]
author_role author
author2 Alves Romariz, Simone Amaro [UNIFESP]
Valente, Maria Fernanda [UNIFESP]
Moraes, Luiz Bruno [UNIFESP]
Covolan, Luciene [UNIFESP]
Calcagnotto, Maria Elisa
Longo, Beatriz Monteiro [UNIFESP]
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Paiva, Daisylea de Souza [UNIFESP]
Alves Romariz, Simone Amaro [UNIFESP]
Valente, Maria Fernanda [UNIFESP]
Moraes, Luiz Bruno [UNIFESP]
Covolan, Luciene [UNIFESP]
Calcagnotto, Maria Elisa
Longo, Beatriz Monteiro [UNIFESP]
dc.subject.eng.fl_str_mv Pentylenetetrazole
Maximal electroshock
Neurosphere
Medial ganglionic eminence
Acute seizure
topic Pentylenetetrazole
Maximal electroshock
Neurosphere
Medial ganglionic eminence
Acute seizure
description Medial ganglionic eminence (MGE) is one of the sources of inhibitory interneurons during development. Following transplantation in postnatal developing brain, MGE cells can increase local inhibition suggesting a possible protection to GABAergic dysfunction in brain disorders, such as epilepsy. Since it has been shown that MGE-derived cells harvested as neurospheres are able to suppress seizures, it might be important to investigate whether these protective effects would change in different seizure models. Here, we used pentylenetetrazole(PTZ) and maximal electroshock (MES)-induced seizure models to test whether the transplantation of MGE cells would increase the threshold to trigger acute seizures. When transplanted into the neocortex (layers 3-4) of neonatal mice (postnatal days 3-4), MGE cells were able to survive and were mainly found in piriform cortex, fimbria, and ventricular wall regions. Additionally, the number of GFP + cells found in the brains of mice induced with PTZ and MES differed significantly and suggests proliferation and larger survival rate of MGE-transplanted cells after PTZ, but not MES-induced seizures. Following transplantation, there was a reduction in the number of animals presenting mild and severe seizures induced by PTZ. Furthermore, MGE-cell transplantation was able to increase threshold to seizures induced by PTZ, but was not able to prevent seizure spread induced by MES. (C) 2017 Elsevier Inc. All rights reserved.
publishDate 2017
dc.date.issued.fl_str_mv 2017
dc.date.accessioned.fl_str_mv 2020-07-13T11:53:21Z
dc.date.available.fl_str_mv 2020-07-13T11:53:21Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Epilepsy & Behavior. San Diego, v. 70, p. 125-130, 2017.
dc.identifier.uri.fl_str_mv https://repositorio.unifesp.br/handle/11600/54560
http://dx.doi.org/10.1016/j.yebeh.2017.03.015
dc.identifier.issn.none.fl_str_mv 1525-5050
dc.identifier.doi.none.fl_str_mv 10.1016/j.yebeh.2017.03.015
dc.identifier.wos.none.fl_str_mv WOS:000402447700020
identifier_str_mv Epilepsy & Behavior. San Diego, v. 70, p. 125-130, 2017.
1525-5050
10.1016/j.yebeh.2017.03.015
WOS:000402447700020
url https://repositorio.unifesp.br/handle/11600/54560
http://dx.doi.org/10.1016/j.yebeh.2017.03.015
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Epilepsy & Behavior
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 125-130
dc.coverage.none.fl_str_mv San Diego
dc.publisher.none.fl_str_mv Academic Press Inc Elsevier Science
publisher.none.fl_str_mv Academic Press Inc Elsevier Science
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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