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Erythropoietin promotes axonal growth in a model of neuronal polarization

机译:促红细胞生成素在神经元极化模型中促进轴突生长

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Erythropoietin (EPO) enhances neurogenesis, neuroprotection and regeneration. Here, we examined the effects of EPO on axonal and dendritic growth in a model of neuronal polarization. EPO did not effect survival or the polarized morphology of hippocampal neurons but its effect on neurite outgrowth depended upon the stage of polarization. When added to neurons in the process of establishing polarity (0-2 days in vitro (DIV)), it enhanced axonal and dendritic growth, while EPO added to early polarized cultures at 3-4 DIV promoted the growth of axons but not dendrites. EPO stimulated the phosphorylation of Akt at serine-473 and co-incubation of the Akt/PI-3 kinase pathway inhibitor LY294002 with EPO abolished its effects on Akt phosphorylation and axonal growth. However, while Leukemia Inhibitory Factor (LIF) similarly stimulated phosphorylation of Akt, it had no effect on axonal or dendritic growth, indicating that AKT phosphorylation is necessary but not sufficient for neurite outgrowth in hippocampal neurons. (C) 2008 Elsevier Inc. All rights reserved.
机译:促红细胞生成素(EPO)增强神经发生,神经保护和再生。在这里,我们检查了神经元极化模型中EPO对轴突和树突状生长的影响。 EPO并不影响存活或海马神经元的极化形态,但其对神经突生长的影响取决于极化的阶段。当在建立极性的过程中(体外0-2天(DIV))添加到神经元中时,它可以增强轴突和树突状细胞的生长,而EPO在3-4 DIV的早期极化培养物中添加可以促进轴突的生长,但不能促进树突状细胞的生长。 EPO刺激了丝氨酸473处的Akt磷酸化,Akt / PI-3激酶途径抑制剂LY294002与EPO共同孵育消除了其对Akt磷酸化和轴突生长的影响。但是,尽管白血病抑制因子(LIF)相似地刺激了Akt的磷酸化,但它对轴突或树突状细胞的生长没有影响,表明AKT磷酸化对于海马神经元的神经突生长是必要的,但不足。 (C)2008 Elsevier Inc.保留所有权利。

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