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Determina??o da atua??o dos RTKs na neuroindu??o e neurog?nese de c?lulas-tronco adultas de tecido de cord?o umbilical humano

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Previous issue date: 2015-08-03 / Introduction : The cellular and physiological changes that accompany the aging process has pronounced effects in neurodegenerative diseases. Factors that produce neurodegeneration do so through different processes that culminate in a common signaling pathway cascade. Stem cells communicate via cellular signaling mechanisms, which is part of a complex system which governs and coordinates activities and cell functions. Understanding the mechanisms and forms of intercellular communication and their relationship in the activation of signaling cascades from the surface receptor to the cell nucleus during neurogenesis, will answer some pertinent questions to the mechanisms of action of stem cells in repair central nervous system. Objective : This study aimed to determine which RTKs being activated during neurogenesis of adult stem cells from human umbilical cord tissue. Methods : Adult stem cells were obtained from human umbilical cord tissue (n = 3) and subjected to specific inducers in neurodifferentiation means. The kit Human Phospho-RTK Array was used for evaluating the phosphorylation of the RTK and the expression determined by realtime PCR. Results : The mesenchymal stem cells obtained from umbilical cord tissue were confirmed by differentiation induction in adipocytes and osteocytes cells. The neurodifferentiation was confirmed by expression of genes that are expressed during neurogenesis in cells and neural cells, as well as immunocytochemistry technique markings which showed nuclear (DAPI) and cell processes (Fluoropan). During the neuroinduction processes and neurodifferentiation the phosphorylation levels of RTKs were variable, with no clear pattern. The Ryk receptor showed no significant changes in their levels of phosphorylation of the three samples studied and the different stages of differentiation, ie, mesenchymal, neuroinductions and neurodifferentiates cells. Conclusions : The tyrosine kinases are actively being phosphorylated during neuroinduction and neurogenesis, with varying standards between the different stages and between different samples, reflecting the variability of human adult stem cells. / Introdu??o : As altera??es celulares e fisiol?gicas que acompanham o processo de envelhecimento tem efeitos pronunciados nas doen?as neurodegenerativas. Os fatores que produzem neurodegenera??o o fazem atrav?s de diferentes processos, que culminam em uma via comum de cascata de sinaliza??o. As c?lulas-tronco se comunicam por mecanismos de sinaliza??o celular, que faz parte de um complexo sistema que governa e coordena as atividades e fun??es celulares. Compreender os mecanismos e as formas de comunica??o intercelular e a sua rela??o na ativa??o das cascatas de sinaliza??o, desde o receptor de superf?cie at? o n?cleo celular, durante a neurog?nese, permitir? responder algumas quest?es pertinentes aos mecanismos de a??o das c?lulas-tronco no reparo do sistema nervoso central. Objetivo : Este estudo teve como objetivo determinar quais os RTKs que est?o sendo ativados durante a neurog?nese de c?lulas-tronco adultas de tecido de cord?o umbilical humano. Metodologia : C?lulas-tronco adultas foram obtidas de tecido de cord?o umbilical humano (n=3) e submetidas a neurodiferencia??o em meios indutores espec?ficos. O kit Human Phospho-RTK Array foi utilizado para avalia??o da fosforila??o dos RTKs e a express?o determinada por PCR em tempo real. Resultados : As c?lulas-tronco mesenquimais obtidas do tecido do cord?o umbilical foram confirmadas atrav?s da indu??o de diferencia??o em c?lulas adip?citas e oste?citas. A neurodiferencia??o foi confirmada atrav?s da express?o de genes que s?o expressos nas c?lulas durante a neurog?nese e em c?lulas neurais, como tamb?m a t?cnica de imunocitoqu?mica que mostrou marca??es nucleares (DAPI) e prolongamentos celulares (Fluoropan). Durante os processos de neuroindu??o e neurodiferencia??o os n?veis de fosforila??o dos RTKs foram vari?veis, sem um padr?o definido. O receptor Ryk n?o apresentou altera??es significativas nos seus n?veis de fosforila??o entre as tr?s amostras estudadas e nas diferentes etapas de diferencia??o, isto ?, c?lulas-tronco mesenquimais, c?lulas neuroinduzidas e c?lulas neurodiferenciadas. Conclus?es : Os receptores tirosina quinases est?o sendo ativamente fosforilados durante a neuroindu??o e neurog?nese, com padr?es vari?veis entre as diferentes etapas e entre diferentes amostras, refletindo a variabilidade das c?lulas-tronco adultas humanas.

Identiferoai:union.ndltd.org:IBICT/oai:tede2.pucrs.br:tede/6311
Date03 August 2015
CreatorsMolina, Rachel Dias
ContributorsMachado, Denise Cantarelli
PublisherPontif?cia Universidade Cat?lica do Rio Grande do Sul, Programa de P?s-Gradua??o em Gerontologia Biom?dica, PUCRS, Brasil, Instituto de Geriatria e Gerontologia
Source SetsIBICT Brazilian ETDs
LanguagePortuguese
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, info:eu-repo/semantics/masterThesis
Formatapplication/pdf
Sourcereponame:Biblioteca Digital de Teses e Dissertações da PUC_RS, instname:Pontifícia Universidade Católica do Rio Grande do Sul, instacron:PUC_RS
Rightsinfo:eu-repo/semantics/openAccess
Relation4438661476953179033, 600, 600, 600, 2296420844541114010, -969369452308786627

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