Requirement for cGMP in Nerve Cell Death Caused by Glutathione Depletion

Author:

Li Yonghong1,Maher Pamela1,Schubert David1

Affiliation:

1. Cellular Neurobiology Laboratory, The Salk Institute for Biological Studies, La Jolla, California 92037; and Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037

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.

Publisher

Rockefeller University Press

Subject

Cell Biology

Reference54 articles.

1. Effects of recombinant human basic FGF and its modified protein CS23 on survival of primary cultured neurons from various regions of fetal rat brain;Abe;Jpn J Pharmacol,1990

2. Programmed cell death and AIDS: significance, perspectives and unanswered questions;Ameisen;Cell Death Diff,1995

3. Role of cyclic GMP in the regulation of neuronal calcium and survival by secreted forms of β-amyloid precursor;Barger;J Neurochem,1995

4. A decrease in intracellular glutathione concentration precedes the onset of apoptosis in murine thymocytes;Beaver;Eur J Cell Biol,1995

5. Retinal degeneration in the rd mouse is caused by a defect in the β subunit of rod cGMP-phosphodiesterase;Bowes;Nature,1990

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