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谷胱甘肽耗竭导致神经细胞死亡中对cGMP的需求。

Requirement for cGMP in nerve cell death caused by glutathione depletion.

作者信息

Li Y, Maher P, Schubert D

机构信息

Cellular Neurobiology Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037, USA.

出版信息

J Cell Biol. 1997 Dec 1;139(5):1317-24. doi: 10.1083/jcb.139.5.1317.

Abstract

Glutathione depletion occurs in several forms of apoptosis and is associated with Parkinson's disease and HIV toxicity. The neurotransmitter glutamate kills immature cortical neurons and a hippocampal nerve cell line via an oxidative pathway associated with glutathione depletion. It is shown here that soluble guanylyl cyclase (sGC) activity is required for nerve cell death caused by glutathione depletion. Inhibitors of sGC block glutamate toxicity and a cGMP analogue potentiates cell death. Glutamate also induces an elevation of cGMP that occurs late in the cell death pathway. The resultant cGMP modulates the increase in intracellular calcium that precedes cell death because sGC inhibitors prevent calcium elevation and the cGMP analogue potentiates the increase in intracellular calcium. These results suggest that the final pathway of glutamate induced nerve cell death is through a cGMP-modulated calcium channel.

摘要

谷胱甘肽耗竭在多种形式的细胞凋亡中都会出现,并且与帕金森病和艾滋病病毒毒性相关。神经递质谷氨酸通过与谷胱甘肽耗竭相关的氧化途径杀死未成熟的皮质神经元和一种海马神经细胞系。本文表明,可溶性鸟苷酸环化酶(sGC)活性是谷胱甘肽耗竭导致神经细胞死亡所必需的。sGC抑制剂可阻断谷氨酸毒性,而一种环磷酸鸟苷(cGMP)类似物会增强细胞死亡。谷氨酸还会诱导cGMP升高,这发生在细胞死亡途径的后期。所产生的cGMP调节细胞死亡之前细胞内钙的增加,因为sGC抑制剂可阻止钙升高,而cGMP类似物会增强细胞内钙的增加。这些结果表明,谷氨酸诱导神经细胞死亡的最终途径是通过cGMP调节的钙通道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9617/2140210/b94bac2e4a3a/JCB.16487f1.jpg

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