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When murine lymphocytes were cultured in a cystine-deficient RPMI-1640 medium containing 10% fetal calf serum, approximately 70% of the cells died in 48 h. In the presence of 5 X 10(-4) M L-cystine, 70-80% of the lymphocytes remained viable under the same condition. The decrease of the viability was also effectively inhibited when cystine was replaced by the following thiol compounds; 2-mercaptoethanol (2-ME), dithiothreitol (DTT), cysteamine and glutathione (GSH). Oxidized DTT, an intramolecular disulfide that was resistant to the reduction by the lymphocytes, did not show a protective effect in contrast to DTT. On the other hand, 2-hydroxyethyldisulfide was readily reduced to 2-ME by the lymphocytes and improved lymphocyte viability as effectively as 2-ME. These observations suggest that thiol groups are responsible for the improvement of lymphocyte viability under a cystine-deficient condition. The viabilities of both T cells and B cells were equally improved by 2-ME. The intracellular level of GSH remained constant in the presence of cystine but dropped rapidly in its absence. 2-ME could not reverse this decrease of GSH level. These protective effects of thiol compounds on lymphocyte viability are discussed in relation to their capacities to activate murine lymphocytes.

journal of pharmacobio-dynamics

Activation of murine lymphocytes by 2-mercaptoethanol and related thiol compounds and its mechanism. II Effect of thiol compounds on the viability of the lymphocytes under a cystine-deficient culture condition.