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The signals of FGFs on the neurogenesis of embryonic stem cells

BACKGROUND: Neural induction is a complex process and the detailed mechanism of FGF-induced neurogenesis remains unclear. METHODS: By using a serum-free neural induction method, we showed that FGF1 dose-dependently promoted the induction of Sox1/N-cadherin/nestin triple positive cells, which represe...

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Detalles Bibliográficos
Autores principales: Chen, Ching-Wen, Liu, Chin-San, Chiu, Ing-Ming, Shen, Shih-Cheng, Pan, Hung-Chuan, Lee, Kun-Hsiung, Lin, Shinn-Zong, Su, Hong-Lin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873938/
https://www.ncbi.nlm.nih.gov/pubmed/20429889
http://dx.doi.org/10.1186/1423-0127-17-33
Descripción
Sumario:BACKGROUND: Neural induction is a complex process and the detailed mechanism of FGF-induced neurogenesis remains unclear. METHODS: By using a serum-free neural induction method, we showed that FGF1 dose-dependently promoted the induction of Sox1/N-cadherin/nestin triple positive cells, which represent primitive neuroblasts, from mouse embryonic stem (ES) cells. RESULTS: We demonstrated that FGF1, FGF2, and FGF4, but not FGF8b, enhanced this neurogenesis. Especially, FGF-enhanced neurogenesis is not mediated through the rescue of the apoptosis or the enhancement of the proliferation of Sox1(+ )cells. We further indicated that the inactivation of c-Jun N-terminal kinase-1 (JNK-1) and extracellular signal-related kinase-2 (ERK-2), but not p38 mitogen-activated protein kinase (MAPK), inhibited the neural formation through the inhibition of ES differentiation, but not through the formation of endomesodermal cells. CONCLUSIONS: These lines of evidence delineated the roles of FGF downstream signals in the early neural differentiation of ES cells.