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神经生长因子依赖性神经突生长测定;化疗诱导的神经病变的研究模型。

Nerve-growth-factor-dependent neurite outgrowth assay; a research model for chemotherapy-induced neuropathy.

作者信息

Geldof A A

机构信息

Department Endocrinology/Urology, Academisch Ziekenhuis Vrije Universiteit, Amsterdam, The Netherlands.

出版信息

J Cancer Res Clin Oncol. 1995;121(11):657-60. doi: 10.1007/BF01218523.

Abstract

The rat clonal pheochromocytoma cell line PC12 can be induced to display neurite outgrowth upon induction with nerve growth factor (NGF). This NGF-dependent neurite outgrowth assay looks a promising model for research on toxic neuropathies. Using this assay we demonstrated that cisplatin caused a dose-dependent reduction of NGF-dependent neurite formation. Increasing doses of NGF, however, proved to exert protective activity against this cisplatin effect at an intermediate and clinically relevant cisplatin concentration of 1 micrograms/ml. Even at a high cisplatin concentration (10 micrograms/ml), the protective action of NGF, although less adequate, was observed. The value and strength of this model for screening neuropathogenic effects of anticancer agents at the cellular level and the possibly therapeutic action of neurotrophins are discussed and demonstrated. Furthermore, in the light of the urgent need for adequate models for neuropathy research, the PC12 neurite outgrowth protection assay may contribute to our knowledge of the mechanisms underlying the development of neuropathy.

摘要

大鼠克隆性嗜铬细胞瘤细胞系PC12在用神经生长因子(NGF)诱导后可被诱导长出神经突。这种依赖NGF的神经突生长测定法看起来是一种研究毒性神经病的很有前景的模型。使用该测定法,我们证明顺铂会导致依赖NGF的神经突形成呈剂量依赖性减少。然而,在顺铂浓度为1微克/毫升这一处于中间范围且与临床相关的浓度下,增加NGF的剂量被证明可对顺铂的这种作用发挥保护活性。即使在高顺铂浓度(10微克/毫升)下,也观察到了NGF的保护作用,尽管其作用不太充分。讨论并展示了该模型在细胞水平筛选抗癌药物神经致病作用以及神经营养因子可能的治疗作用方面的价值和优势。此外,鉴于迫切需要适用于神经病研究的模型,PC12神经突生长保护测定法可能有助于我们了解神经病发展的潜在机制。

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