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Inhibition of the rate-limiting enzyme HMG-CoA reductase with atorvastatin suppressed proliferation in both non-arrested cells and released CD8 + T cells (Fig

Figure 1: Chemical structure of Glutathione [source: Accessed: 10 Oct 2012] The presence of the reactive sulphydryl group (originating from the cysteine residue) gives rise to GSHs nucleophilic nature and so it reacts readily with electrophiles which can present high risk of toxicity to the cell by causing oxidative damage such as lipid peroxidation to cell membranes, and interfering with the activity of essential proteins and DNA synthesis

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Synthesis of glutathione in leaves of transgenic poplar overexpressing -glutamylcysteine synthetase