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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Functional and immunocytochemical characterization of the creatine transporter in rat hippocampal neurons.
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Functional and immunocytochemical characterization of the creatine transporter in rat hippocampal neurons.

机译:大鼠海马神经元中肌酸转运蛋白的功能和免疫细胞化学表征。

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摘要

Creatine uptake by neurons requires a specific creatine transporter (CRT). The purpose of the present work was to investigate the activity and localization of the CRT in primary cultures of hippocampal neurons obtained from 18-day rat embryos. Creatine uptake increased as the neurons differentiated in culture. Immunofluorescence microscopy showed most of the CRT was associated with dendrites, although some CRT was present in axons and axon terminals. Neurons contained high levels of Na(+)-dependent creatine transport activity (K(m) = 45.5 muM; V(max), 1719 pmol creatine/min/mg protein) which was inhibited by competitive inhibitors of the CRT. The IC(50) for guanidinoacetate, a precursor of creatine, was 712 muM, approximately 15-fold higher than the K(m) for creatine. Incubation of neurons with 1 mM creatine resulted in the accumulation of high levels of creatine which affected the V(max) but not the K(m) for creatine transport. The rate of creatine release from neurons increased in the absence of Na(+) showing the importance of the electrochemical gradient for creatine retention. This is the first detailed study of the CRT in neurons and identifies primary cultures of rat hippocampal neurons as a good model for future studies of the CRT in relation to the effects of creatine on neuronal function and viability.
机译:神经元摄取肌酸需要特定的肌酸转运蛋白(CRT)。本工作的目的是研究从18天大鼠胚胎获得的海马神经元原代培养物中CRT的活性和定位。肌酸的摄取随着神经元在培养物中的分化而增加。免疫荧光显微镜检查显示,大多数CRT与树突有关,尽管在轴突和轴突末端存在一些CRT。神经元包含高水平的Na(+)依赖性肌酸转运活性(K(m)= 45.5μM; V(max),1719 pmol肌酸/ min / mg蛋白),这受CRT竞争性抑制剂抑制。胍基乙酸盐(肌酸的前体)的IC(50)为712μM,比肌酸的K(m)高约15倍。用1 mM肌酸温育神经元会导致高水平肌酸的积累,从而影响肌酸转运的V(max)而不是K(m)。在没有Na(+)的情况下,神经元释放肌酸的速率增加,这表明电化学梯度对肌酸保留的重要性。这是对神经元中的CRT的首次详细研究,并且确定了大鼠海马神经元的原代培养物,作为今后研究CRT与肌酸对神经元功能和生存能力相关的良好模型。

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