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首页> 外文期刊>Brain research >In vitro characteristics of Valproic acid and all-trans-retinoic acid and their combined use in promoting neuronal differentiation while suppressing astrocytic differentiation in neural stem cells
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In vitro characteristics of Valproic acid and all-trans-retinoic acid and their combined use in promoting neuronal differentiation while suppressing astrocytic differentiation in neural stem cells

机译:丙戊酸和全反式维甲酸的体外特性及其组合用于促进神经元分化,同时抑制神经干细胞的星形细胞分化

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Multipotent neural stem cells (NSCs) are currently under investigation as a candidate treatment for central nervous system (CNS) injury because of their potential to compensate for neuronal damage and to reconstruct disrupted neuronal connections. To maximize the regenerative effect of the derived neurons and to minimize the side effects of the derived astrocytes, it is necessary to regulate the fate determination of NSCs to produce more neurons and fewer astrocytes. Both valproic acid (VPA) and all-trans-retinoic acid (ATRA), two clinically established drugs, induce neuronal differentiation and facilitate neurite outgrowth at the expense of astrocytic differentiation in NSCs. However, the time-dependent activities and the long-term treatment effects of these drugs have not been explored in NSCs. More importantly, the efficacies of VPA and ATRA in neuronal promotion and astrocytic suppression remain unclear. In this study, we compare the time-dependent characteristics of VPA and ATRA in NSC differentiation and neurite outgrowth in vitro and, for the first time, demonstrate the improved efficacy of their combined application in neuronal induction and astrocrtic suppression. These significant effects are closely coupled to the altered expression of a neurogenic transcription factor, a Wnt signaling component, a cell cycle regulator and a neural growth factor, indicating an underlying cross-talk between the mechanisms of action of ATRA and VPA. These findings indicate that a novel strategy combining these two therapeutic drugs may improve the restorative effect of NSC transplantation by altering the expression of their interconnected targets for fate determination. (C) 2014 Elsevier B.V. All rights reserved.
机译:目前,多能神经干细胞(NSC)正在研究中枢神经系统(CNS)损伤的候选治疗方法,因为它们具有补偿神经元损伤和重建神经元连接的潜力。为了最大化衍生神经元的再生作用并最小化衍生星形胶质细胞的副作用,有必要调节NSC的命运确定,以产生更多的神经元和更少的星形胶质细胞。丙戊酸(VPA)和全反式维甲酸(ATRA)是两种临床上公认的药物,它们以神经细胞的星形胶质细胞分化为代价,诱导神经元分化并促进神经突生长。但是,尚未在NSC中探讨这些药物的时间依赖性活性和长期治疗效果。更重要的是,尚不清楚VPA和ATRA在神经元促进和星形细胞抑制中的作用。在这项研究中,我们比较了VPA和ATRA在NSC分化和神经突向外生长中随时间变化的特征,并首次证明了它们在神经元诱导和星形胶质抑制中的联合应用具有更高的疗效。这些重要作用与神经源性转录因子,Wnt信号转导成分,细胞周期调节剂和神经生长因子表达的改变密切相关,表明ATRA和VPA的作用机理之间存在潜在的相互影响。这些发现表明,结合这两种治疗药物的新策略可以通过改变命运决定因素的相互联系来改善NSC移植的修复效果。 (C)2014 Elsevier B.V.保留所有权利。

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