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神经节苷脂GM1不会引发,但会增强神经生长因子依赖性感觉神经元的轴突再生。

Ganglioside GM1 does not initiate, but enhances neurite regeneration of nerve growth factor-dependent sensory neurones.

作者信息

Doherty P, Dickson J G, Flanigan T P, Walsh F S

出版信息

J Neurochem. 1985 Apr;44(4):1259-65. doi: 10.1111/j.1471-4159.1985.tb08752.x.

Abstract

An enzyme-linked immunoadsorbent assay (ELISA) for neurofilament protein was utilised to quantify the effect of exogenous ganglioside on neurite regeneration in cultures of dorsal root ganglion neurones. In contrast to nerve growth factor (NGF), ganglioside GM1 (100 micrograms/ml) failed to support neuronal survival and neurite regeneration as quantified by the ELISA assay and confirmed by morphological criteria. However, the simultaneous presence of GM1 (100 micrograms/ml) and NGF (0.5-5 ng/ml) throughout a 5-day period of culture resulted in an enhancement of previously reported NGF-induced increases in the expression of neurofilament protein. Further, the addition of GM1 (0-200 micrograms/ml) at 48 h in vitro to cultures initially established in the presence of 5 ng/ml NGF substantially increased the subsequent expression of neurofilament protein, this response being both independent of and not potentiated by NGF. The results in the present system suggest that GM1 cannot initiate a programme of neurite regeneration; however, GM1 can enhance this process with the response being secondary to the effect of NGF.

摘要

采用神经丝蛋白的酶联免疫吸附测定(ELISA)来量化外源性神经节苷脂对背根神经节神经元培养物中神经突再生的影响。与神经生长因子(NGF)不同,ELISA测定显示神经节苷脂GM1(100微克/毫升)不能支持神经元存活和神经突再生,形态学标准也证实了这一点。然而,在5天的培养期内同时存在GM1(100微克/毫升)和NGF(0.5 - 5纳克/毫升),导致先前报道的NGF诱导的神经丝蛋白表达增加得到增强。此外,在体外培养48小时时向最初在5纳克/毫升NGF存在下建立的培养物中添加GM1(0 - 200微克/毫升),显著增加了随后神经丝蛋白的表达,这种反应既不依赖于NGF,也不会被NGF增强。本系统中的结果表明,GM1不能启动神经突再生程序;然而,GM1可以增强这一过程,其反应是NGF作用的继发效应。

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