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神经基础培养基对成熟皮质神经元的毒性作用。

Neurobasal medium toxicity on mature cortical neurons.

作者信息

Maggioni Daniele, Monfrini Marianna, Ravasi Maddalena, Tredici Giovanni, Scuteri Arianna

机构信息

Department of Surgery and Translational Medicine, University of Milan-Bicocca, Monza, Italy.

出版信息

Neuroreport. 2015 Apr 15;26(6):320-4. doi: 10.1097/WNR.0000000000000343.

Abstract

Neurobasal medium (NBM) is a widely used medium for neuronal cultures, originally formulated to support survival of rat hippocampal neurons, but then optimized for several other neuronal subtypes. In the present study, the toxic effect of NBM on long-term cortical neuron cultures has been reported and investigated. A significant neuronal cell loss was observed 24 h after the total medium change performed at days in vitro 10. The neurotoxic effect was specifically because of NBM-A, a commercially derived modification of classic NBM, as neurons exposed to minimum essential medium for 24 h did not show the same mortality rate. We showed that the toxic effect was mediated by the N-methyl-D-aspartate receptor (NMDAr) as its inactivation partly prevented NBM-induced neuronal loss, and the addition of NMDAr activators, such as L-cysteine or glycine to minimum essential medium, reproduced the same toxicity rate observed in NBM. Besides the toxicity associated with NMDAr activation, the decreased antioxidative defenses also worsen (because of glutathione depletion) neuronal death, thus amplifying the effect of excitotoxic amino acids. Indeed, glutathione supplementation by the addition of its precursor N-acetyl-cysteine resulted in an increase in neuronal survival that partially prevented NBM-A toxicity. These results evidenced, on the one hand, the unsuitability of NBM-A for long-term neuronal culture, and on the other, they highlight the importance of selection of more suitable culture conditions.

摘要

神经基础培养基(NBM)是一种广泛用于神经元培养的培养基,最初设计用于支持大鼠海马神经元的存活,后来针对其他几种神经元亚型进行了优化。在本研究中,已报道并研究了NBM对长期皮质神经元培养的毒性作用。在体外培养第10天进行全培养基更换后24小时,观察到显著的神经元细胞损失。神经毒性作用具体是由于NBM-A引起的,NBM-A是经典NBM的一种商业衍生变体,因为暴露于最低限度基本培养基24小时的神经元没有显示出相同的死亡率。我们表明,毒性作用是由N-甲基-D-天冬氨酸受体(NMDAr)介导的,因为其失活部分预防了NBM诱导的神经元损失,并且向最低限度基本培养基中添加NMDAr激活剂,如L-半胱氨酸或甘氨酸,重现了在NBM中观察到的相同毒性率。除了与NMDAr激活相关的毒性外,抗氧化防御能力的降低(由于谷胱甘肽耗竭)也会加剧神经元死亡,从而放大兴奋性毒性氨基酸的作用。事实上,通过添加其前体N-乙酰半胱氨酸补充谷胱甘肽导致神经元存活率增加,部分预防了NBM-A的毒性。这些结果一方面证明了NBM-A不适合长期神经元培养,另一方面,它们突出了选择更合适培养条件的重要性。

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