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A Potential Excitability Was Induced by Basic Fibroblast Growth Factor during Early Differentiation of Neurons from Mouse Embryonic Stem Cells in vitro

机译:在小鼠胚胎干细胞神经元的早期分化过程中,碱性成纤维细胞生长因子诱导了潜在的兴奋性。

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We report that basic fibroblast growth factor (bFGF) induces the release of glutamate in ES-derived neurons during early stages of differentiation. Changes of Ca2+ concentration labeled by fluorescence intensity occurred in response to minimal concentrations of glutamate. The Ca2+ concentration was changed more rapidly by bFGF than by glutamate during the early stages of differentiation of ES-derived neurons. High concentrations of the inhibitor MK801, an N-methyl-D-aspartate (NMDA) receptor antagonist applied before bFGF stimulation caused a dramatic decrease of fluorescence intensity in neurons derived from both hippocampal and ES cells. These results showed that bFGF induces glutamate release and an increase of [Ca2+] in neurons during early stages of differentiation, and that the increase of [Ca2+] can be inhibited by MK801. Therefore, we concluded that bFGF serves not only as a neurotrophin but also as a stimulator of excitability during the differentiation of ES cells into neurons
机译:我们报告基本成纤维细胞生长因子(bFGF)诱导分化的早期阶段在ES衍生的神经元中谷氨酸的释放。荧光强度标记的Ca 2 + 浓度的变化是响应于最低浓度的谷氨酸而发生的。在ES衍生神经元分化的早期,bFGF比谷氨酸改变Ca 2 + 的速度更快。在bFGF刺激之前使用高浓度的抑制剂MK801(一种N-甲基-D-天冬氨酸(NMDA)受体拮抗剂)会导致海马和ES细胞神经元的荧光强度急剧下降。这些结果表明,bFGF在分化的早期阶段诱导神经元中谷氨酸的释放和[Ca 2 + ]的增加,而[Ca 2 + ]的增加可以被MK801抑制。因此,我们得出结论,在ES细胞分化为神经元的过程中,bFGF不仅可以作为神经营养蛋白,而且可以作为兴奋性刺激物。

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