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Neuronal differentiation of embryonic midbrain cells by upregulation of peroxisome proliferator-activated receptor-gamma via the JNK-dependent pathway.
Park, Ki Sook; Lee, Rhee Da; Kang, Sun-Kyung; Han, Soon Young; Park, Kui Lae; Yang, Ki Hwa; Song, Youn Sook; Park, Hye Ji; Lee, Yoot Mo; Yun, Yeo Pyo; Oh, Ki Wan; Kim, Dae Joong; Yun, Young Won; Hwang, Se Jin; Lee, Sung Eun; Hong, Jin Tae.
Afiliação
  • Park KS; National Institute of Toxicological Research, Korea Food and Drug Administration, Seoul, South Korea.
Exp Cell Res ; 297(2): 424-33, 2004 Jul 15.
Article em En | MEDLINE | ID: mdl-15212945
ABSTRACT
Our previous study showed that the peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonist 15-deoxy-PGJ(2) has the promoting ability to differentiate neuronal PC12 cells. To expand our study, the effect of 15-deoxy-PGJ(2) on the differentiation of embryonic midbrain cells into dopaminergic neuronal cells was investigated in this study. The relationship between cell differentiation with activation of PPAR-gamma and the possible signal pathway were also investigated. 15-Deoxy-PGJ(2) increased neurite extension, a typical characteristic of the differentiation of embryonic midbrain cells isolated from 12-day rat embryos in a dose-dependent manner. The expression of differentiation markers, neurofilament, tyrosine hydroxylase, and nestin, was also increased by the treatment of 15-deoxy-PGJ(2). Consistent with the increasing effect on cell differentiation, 15-deoxy-PGJ(2) increased the expression and transcriptional activity of PPAR-gamma in cultured embryonic midbrain cells. In addition, the expression of PPAR-gamma and NeuN in the differentiated neuron of fetus (17 days) and adult rat brain was co-localized. Furthermore, treatment of PPAR-gamma antagonist bisphenol A diglycidyl ether blocked 15-deoxy-PGJ(2)-induced neuronal differentiation of embryonic midbrain cells and expression of PPAR-gamma. To elucidate the possible signal pathway, the activation of mitogenic-activated protein (MAP) kinase family was determined. 15-Deoxy-PGJ(2) (0.5 microM) increased activation of Jun N-terminal kinase (JNK) and p38 kinase but not extra-signal response kinase (ERK). In addition, NGF (50 ng/ml) further increased the 15-deoxy-PGJ(2)-induced JNK activation. Moreover, pretreatment of specific inhibitor of JNK SP600125 blocked the 15-deoxy-PGJ(2)-induced JNK activation. This inhibition correlated well with the inhibition of neurite extension and expression of PPAR-gamma induced by 15-deoxy-PGJ(2). The present results therefore indicate that 15-deoxy-PGJ(2) stimulates differentiation of embryonic midbrain cells into dopaminergic neuronal cells, and its effect may be PPAR-gamma and JNK signal pathway dependent.
Assuntos
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Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Transdução de Sinais / Diferenciação Celular / Regulação para Cima / Proteínas Proto-Oncogênicas c-jun / Receptores Citoplasmáticos e Nucleares / Neurônios Limite: Animals Idioma: En Ano de publicação: 2004 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Transdução de Sinais / Diferenciação Celular / Regulação para Cima / Proteínas Proto-Oncogênicas c-jun / Receptores Citoplasmáticos e Nucleares / Neurônios Limite: Animals Idioma: En Ano de publicação: 2004 Tipo de documento: Article