Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.1/14045 |
Resumo: | Nitric oxide (NO) is well established as a regulator of neurogenesis. NO increases the proliferation of neural stem cells (NSC), and is essential for hippocampal injury-induced neurogenesis following an excitotoxic lesion. One of the mechanisms underlying non-classical NO cell signaling is protein S-nitrosylation. This post-translational modification consists in the formation of a nitrosothiol group (R-SNO) in cysteine residues, which can promote formation of other oxidative modifications in those cysteine residues. S-nitrosylation can regulate many physiological processes, including neuronal plasticity and neurogenesis. In this work, we aimed to identify S-nitrosylation targets of NO that could participate in neurogenesis. In NSC, we identified a group of proteins oxidatively modified using complementary techniques of thiol redox proteomics. S-nitrosylation of some of these proteins was confirmed and validated in a seizure mouse model of hippocampal injury and in cultured hippocampal stem cells. The identified S-nitrosylated proteins are involved in the ERK/MAPK pathway and may be important targets of NO to enhance the proliferation of NSC. |
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Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomicsNitric oxideHippocampusS-nitrosylationSeizuresNeural stem cellsNeurogenesisNitric oxide (NO) is well established as a regulator of neurogenesis. NO increases the proliferation of neural stem cells (NSC), and is essential for hippocampal injury-induced neurogenesis following an excitotoxic lesion. One of the mechanisms underlying non-classical NO cell signaling is protein S-nitrosylation. This post-translational modification consists in the formation of a nitrosothiol group (R-SNO) in cysteine residues, which can promote formation of other oxidative modifications in those cysteine residues. S-nitrosylation can regulate many physiological processes, including neuronal plasticity and neurogenesis. In this work, we aimed to identify S-nitrosylation targets of NO that could participate in neurogenesis. In NSC, we identified a group of proteins oxidatively modified using complementary techniques of thiol redox proteomics. S-nitrosylation of some of these proteins was confirmed and validated in a seizure mouse model of hippocampal injury and in cultured hippocampal stem cells. The identified S-nitrosylated proteins are involved in the ERK/MAPK pathway and may be important targets of NO to enhance the proliferation of NSC.PTDC/QUI-QFI/29319/2017; UID/BIM/04773/2019ElsevierSapientiaSantos, Ana IsabelLourenco, Ana S.Simão, SóniaMarques-da-Silva, DorindaSantos, Daniela F.Carvalho, Ana Paula Onofre dePereira, Ana CatarinaIzquierdo-Álvarez, AliciaRamos, ElenaMorato, EsperanzaMarina, AnabelMartínez-Ruiz, AntonioAraújo, Inês2020-06-22T11:13:43Z2020-052020-05-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/14045eng2213-231710.1016/j.redox.2020.101457info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-24T10:26:16Zoai:sapientia.ualg.pt:10400.1/14045Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:05:06.868023Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics |
title |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics |
spellingShingle |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics Santos, Ana Isabel Nitric oxide Hippocampus S-nitrosylation Seizures Neural stem cells Neurogenesis |
title_short |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics |
title_full |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics |
title_fullStr |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics |
title_full_unstemmed |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics |
title_sort |
Identification of new targets of S-nitrosylation in neural stem cells by thiol redox proteomics |
author |
Santos, Ana Isabel |
author_facet |
Santos, Ana Isabel Lourenco, Ana S. Simão, Sónia Marques-da-Silva, Dorinda Santos, Daniela F. Carvalho, Ana Paula Onofre de Pereira, Ana Catarina Izquierdo-Álvarez, Alicia Ramos, Elena Morato, Esperanza Marina, Anabel Martínez-Ruiz, Antonio Araújo, Inês |
author_role |
author |
author2 |
Lourenco, Ana S. Simão, Sónia Marques-da-Silva, Dorinda Santos, Daniela F. Carvalho, Ana Paula Onofre de Pereira, Ana Catarina Izquierdo-Álvarez, Alicia Ramos, Elena Morato, Esperanza Marina, Anabel Martínez-Ruiz, Antonio Araújo, Inês |
author2_role |
author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Sapientia |
dc.contributor.author.fl_str_mv |
Santos, Ana Isabel Lourenco, Ana S. Simão, Sónia Marques-da-Silva, Dorinda Santos, Daniela F. Carvalho, Ana Paula Onofre de Pereira, Ana Catarina Izquierdo-Álvarez, Alicia Ramos, Elena Morato, Esperanza Marina, Anabel Martínez-Ruiz, Antonio Araújo, Inês |
dc.subject.por.fl_str_mv |
Nitric oxide Hippocampus S-nitrosylation Seizures Neural stem cells Neurogenesis |
topic |
Nitric oxide Hippocampus S-nitrosylation Seizures Neural stem cells Neurogenesis |
description |
Nitric oxide (NO) is well established as a regulator of neurogenesis. NO increases the proliferation of neural stem cells (NSC), and is essential for hippocampal injury-induced neurogenesis following an excitotoxic lesion. One of the mechanisms underlying non-classical NO cell signaling is protein S-nitrosylation. This post-translational modification consists in the formation of a nitrosothiol group (R-SNO) in cysteine residues, which can promote formation of other oxidative modifications in those cysteine residues. S-nitrosylation can regulate many physiological processes, including neuronal plasticity and neurogenesis. In this work, we aimed to identify S-nitrosylation targets of NO that could participate in neurogenesis. In NSC, we identified a group of proteins oxidatively modified using complementary techniques of thiol redox proteomics. S-nitrosylation of some of these proteins was confirmed and validated in a seizure mouse model of hippocampal injury and in cultured hippocampal stem cells. The identified S-nitrosylated proteins are involved in the ERK/MAPK pathway and may be important targets of NO to enhance the proliferation of NSC. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-06-22T11:13:43Z 2020-05 2020-05-01T00:00:00Z |
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.uri.fl_str_mv |
http://hdl.handle.net/10400.1/14045 |
url |
http://hdl.handle.net/10400.1/14045 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2213-2317 10.1016/j.redox.2020.101457 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799133289969090560 |