Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais

Detalhes bibliográficos
Autor(a) principal: Schmiddel, Felipe
Data de Publicação: 2022
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/001300000hkc5
Texto Completo: http://repositorio.ufsm.br/handle/1/25014
Resumo: Intermediate and extrinsic intrinsic stimuli contribute to the growth of progenitor cells (NPCs). Extracellular stimuli cause NPCs to differentiate into glial cells and neurons. At the intracellular level, as signaling pathways, cyclic adenosine (cAMP) expression is also dependent on the control of gene expression, such as cell transition processes and neurite outgrowth. The production of cAMP is directly related to the increase in deneurite growth in different cell lines, but the effects of this second line of growth on NPCs are not yet fully understood. To investigate the effects of cAMP on an augmented model of NPCs, which are augmented of the model of NPCs, which increase the capacity of NPCs, which encompass the neurospheres of most neural processes that extend into the early stages of development. This is, therefore, an excellent in vitro study model to assess the influence of cAMP-dependent pathways on these processes. Therefore, in this study, we investigated the effect of cAMP in the study of cAMPs that contemplate an increase in the development of neurogenesis, neurogenesis, gliogenesis and migrations in NPCs in vitro. We observed that the cAMP of the NPCs is potentiated, dibutyryl cAMP (db-cAMP) and pertussis toxin (PTX). The db-cAMP increased the measurement, of the NPCs, in which it increased the frequency of neuronal positive for beta-3-tublin and MAP2+, neurite outgrowth cells. Neural migratory PTX was further configured in treated NPCs or with a reduced number of cells that have distanced themselves from neuroscience. It is concluded that cAMP signaling pathways stimulate neuron growth and stimulate NPC migrations during cell media.
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spelling Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neuraisEffects of intracellular cAMP on differentiation of neural progenitor cellsMonofosfato de adenosinaNeuroesferasNPCsProliferação celularDiferenciação de NPCsAdenosine monophosphateNeurospheresCell proliferationNPCs differentiationCNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIAIntermediate and extrinsic intrinsic stimuli contribute to the growth of progenitor cells (NPCs). Extracellular stimuli cause NPCs to differentiate into glial cells and neurons. At the intracellular level, as signaling pathways, cyclic adenosine (cAMP) expression is also dependent on the control of gene expression, such as cell transition processes and neurite outgrowth. The production of cAMP is directly related to the increase in deneurite growth in different cell lines, but the effects of this second line of growth on NPCs are not yet fully understood. To investigate the effects of cAMP on an augmented model of NPCs, which are augmented of the model of NPCs, which increase the capacity of NPCs, which encompass the neurospheres of most neural processes that extend into the early stages of development. This is, therefore, an excellent in vitro study model to assess the influence of cAMP-dependent pathways on these processes. Therefore, in this study, we investigated the effect of cAMP in the study of cAMPs that contemplate an increase in the development of neurogenesis, neurogenesis, gliogenesis and migrations in NPCs in vitro. We observed that the cAMP of the NPCs is potentiated, dibutyryl cAMP (db-cAMP) and pertussis toxin (PTX). The db-cAMP increased the measurement, of the NPCs, in which it increased the frequency of neuronal positive for beta-3-tublin and MAP2+, neurite outgrowth cells. Neural migratory PTX was further configured in treated NPCs or with a reduced number of cells that have distanced themselves from neuroscience. It is concluded that cAMP signaling pathways stimulate neuron growth and stimulate NPC migrations during cell media.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESEstímulos intrínsecos e extrínsecos contribuem para o crescimento e diferenciação de células progenitoras neurais (NPCs). Os estímulos extracelulares fazem com que as NPCs se diferenciem em células gliais e neurônios. Já no nível intracelular, as vias de sinalização, como os processos dependentes de monofosfato de adenosina cíclico (AMPc), também controlam a expressão gênica, a proliferação, a migração celular e o crescimento de neuritos. A produção de AMPc está diretamente relacionada com o aumento do crescimento de neuritos em diferentes linhagens celulares, mas os efeitos deste segundo mensageiro em NPCs embrionários ainda não foram totalmente esclarecidos. Para investigar o efeito do aumento do AMPc sobre a proliferação, diferenciação de NPCs, utilizamos um modelo de neuroesferas, que são agregados celulares flutuantes de NPCs, que contemplam a maior parte dos processos que ocorrem nos estágios iniciais do desenvolvimento neural. Este é, portanto, um excelente modelo de estudo in vitro para avaliar a influência das vias dependentes de AMPc nestes processos. Portanto, neste estudo investigamos o efeito do aumento do AMPc nos processos de desenvolvimento neural que contemplam a proliferação, o crescimento de neuritos, neurogênese, gliogênese e migração observados em NPCs in vitro. Observamos que a proliferação das NPCs é potencializada por forscolina, dibutiril AMPc (db-AMPc) e toxina pertussis (PTX). O db- AMPc aumentou a diferenciação das NPCs em neurônios, na medida em que aumentou a frequência de células neuronais positivas para beta-3-tubulina e MAP2+, além de promover o crescimento de neuritos. Observamos ainda, que a migração neural foi amplamente restrita em NPCs tratados com db-cAMP ou PTX em comparação com controles, evidenciado por um número reduzido de células que se distanciaram das neuroesferas. Concluímos que as vias de sinalização do AMPc estimulam o crescimento de neuritos e bloqueiam a migração de NPCs durante a diferenciação celular.Universidade Federal de Santa MariaBrasilFarmacologiaUFSMPrograma de Pós-Graduação em FarmacologiaCentro de Ciências da SaúdeMello, Carlos Fernando dehttp://lattes.cnpq.br/3913887223894236Oliveira, Mauro SchneiderOliveira, Karen Renata Herculano MatosSchmiddel, Felipe2022-06-22T17:36:18Z2022-06-22T17:36:18Z2022-02-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://repositorio.ufsm.br/handle/1/25014ark:/26339/001300000hkc5porAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-08-23T14:16:45Zoai:repositorio.ufsm.br:1/25014Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2022-08-23T14:16:45Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
Effects of intracellular cAMP on differentiation of neural progenitor cells
title Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
spellingShingle Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
Schmiddel, Felipe
Monofosfato de adenosina
Neuroesferas
NPCs
Proliferação celular
Diferenciação de NPCs
Adenosine monophosphate
Neurospheres
Cell proliferation
NPCs differentiation
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
title_short Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
title_full Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
title_fullStr Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
title_full_unstemmed Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
title_sort Efeitos do AMPc intracelular sobre a diferenciação de células progenitoras neurais
author Schmiddel, Felipe
author_facet Schmiddel, Felipe
author_role author
dc.contributor.none.fl_str_mv Mello, Carlos Fernando de
http://lattes.cnpq.br/3913887223894236
Oliveira, Mauro Schneider
Oliveira, Karen Renata Herculano Matos
dc.contributor.author.fl_str_mv Schmiddel, Felipe
dc.subject.por.fl_str_mv Monofosfato de adenosina
Neuroesferas
NPCs
Proliferação celular
Diferenciação de NPCs
Adenosine monophosphate
Neurospheres
Cell proliferation
NPCs differentiation
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
topic Monofosfato de adenosina
Neuroesferas
NPCs
Proliferação celular
Diferenciação de NPCs
Adenosine monophosphate
Neurospheres
Cell proliferation
NPCs differentiation
CNPQ::CIENCIAS BIOLOGICAS::FARMACOLOGIA
description Intermediate and extrinsic intrinsic stimuli contribute to the growth of progenitor cells (NPCs). Extracellular stimuli cause NPCs to differentiate into glial cells and neurons. At the intracellular level, as signaling pathways, cyclic adenosine (cAMP) expression is also dependent on the control of gene expression, such as cell transition processes and neurite outgrowth. The production of cAMP is directly related to the increase in deneurite growth in different cell lines, but the effects of this second line of growth on NPCs are not yet fully understood. To investigate the effects of cAMP on an augmented model of NPCs, which are augmented of the model of NPCs, which increase the capacity of NPCs, which encompass the neurospheres of most neural processes that extend into the early stages of development. This is, therefore, an excellent in vitro study model to assess the influence of cAMP-dependent pathways on these processes. Therefore, in this study, we investigated the effect of cAMP in the study of cAMPs that contemplate an increase in the development of neurogenesis, neurogenesis, gliogenesis and migrations in NPCs in vitro. We observed that the cAMP of the NPCs is potentiated, dibutyryl cAMP (db-cAMP) and pertussis toxin (PTX). The db-cAMP increased the measurement, of the NPCs, in which it increased the frequency of neuronal positive for beta-3-tublin and MAP2+, neurite outgrowth cells. Neural migratory PTX was further configured in treated NPCs or with a reduced number of cells that have distanced themselves from neuroscience. It is concluded that cAMP signaling pathways stimulate neuron growth and stimulate NPC migrations during cell media.
publishDate 2022
dc.date.none.fl_str_mv 2022-06-22T17:36:18Z
2022-06-22T17:36:18Z
2022-02-25
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://repositorio.ufsm.br/handle/1/25014
dc.identifier.dark.fl_str_mv ark:/26339/001300000hkc5
url http://repositorio.ufsm.br/handle/1/25014
identifier_str_mv ark:/26339/001300000hkc5
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Farmacologia
UFSM
Programa de Pós-Graduação em Farmacologia
Centro de Ciências da Saúde
publisher.none.fl_str_mv Universidade Federal de Santa Maria
Brasil
Farmacologia
UFSM
Programa de Pós-Graduação em Farmacologia
Centro de Ciências da Saúde
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
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institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
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