Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure induction
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1016/j.yebeh.2017.03.015 https://repositorio.unifesp.br/handle/11600/54560 |
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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Transplantation of inhibitory precursor cells from medial ganglionic eminence produces distinct responses in two different models of acute seizure inductionPentylenetetrazoleMaximal electroshockNeurosphereMedial ganglionic eminenceAcute seizureMedial 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.Univ 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 ScienceFAPESPCNPqAcademic Press Inc Elsevier Science2020-07-13T11:53:21Z2020-07-13T11:53:21Z2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion125-130http://dx.doi.org/10.1016/j.yebeh.2017.03.015Epilepsy & Behavior. San Diego, v. 70, p. 125-130, 2017.10.1016/j.yebeh.2017.03.0151525-5050https://repositorio.unifesp.br/handle/11600/54560WOS:000402447700020engEpilepsy & BehaviorSan Diegoinfo:eu-repo/semantics/openAccessPaiva, 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]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2021-10-05T22:05:35Zoai:repositorio.unifesp.br/:11600/54560Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652021-10-05T22:05:35Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.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.por.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.none.fl_str_mv |
2017 2020-07-13T11:53:21Z 2020-07-13T11:53:21Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.yebeh.2017.03.015 Epilepsy & Behavior. San Diego, v. 70, p. 125-130, 2017. 10.1016/j.yebeh.2017.03.015 1525-5050 https://repositorio.unifesp.br/handle/11600/54560 WOS:000402447700020 |
url |
http://dx.doi.org/10.1016/j.yebeh.2017.03.015 https://repositorio.unifesp.br/handle/11600/54560 |
identifier_str_mv |
Epilepsy & Behavior. San Diego, v. 70, p. 125-130, 2017. 10.1016/j.yebeh.2017.03.015 1525-5050 WOS:000402447700020 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.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 |
biblioteca.csp@unifesp.br |
_version_ |
1814268268171493376 |