IGF-I aumenta a proliferação de células da retina em cultura: vias de sinalização envolvidas

Detalhes bibliográficos
Ano de defesa: 2009
Autor(a) principal: Medina, Simone Vidal
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Programa de Pós-graduação em Neuroimunologia
Neuroimunologia
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
M1
Link de acesso: https://app.uff.br/riuff/handle/1/18421
Resumo: IGF-I is a growth factor playing a role in cell survival, cell proliferation and cell differentiation. The purpose of this work was to study, in vitro, the effect of IGF-I on retinal cell proliferation. Our results show that treatment with IGF-I induces a 50% increase in cellular proliferation. This effect was dose and time dependent. The greater response was obtained with 10ng/mL IGF-I after 24-48h in culture. However after 72h, cultures treated with IGF-I did not exhibit an increase in cell proliferation. The effect of IGF-I involves the stimulation of several intracellular pathways including activation of PI-3 kinase, phospholipase C, PKC d, MAPK, JNK and Src. Our results suggest that following IGF-I treatment the metalloproteinase 9 and EGF receptors are stimulated. When we either blocked the vesicular release of polypeptides or the internalization of membrane receptors the effect of IGF-I was inhibited. Taken together our results show that the proliferative effect of IGF-I depends on the activation of EGF receptors and on the activation of distinct intracellular pathways. Since the IGF-I effect was observed only during the first 48h in culture we may suggest a regulatory role of this trophic factor in the control of cellular proliferation of retinal cells.