Previously, lit was shown that glycine prevented increases in intracellular
calcium ([Ca2+](i)) in Kupffer cells. Since Kupffer cells and T lymphocyte
s are derived from the same pluripotent stem cell, it was hypothesized that
glycine mould prevent increases in [Ca2+](i) in lymphocytes and inhibit ce
ll proliferation. Lymphocyte proliferation was measured in one-way MLC with
spleen cells from DA and Lewis rats and in enriched T lymphocyte preparati
ons stimulated by immobilized anti-CD3 Ab, Glycine caused a dose-dependent
decrease in cell proliferation to about 40% of control. Con A caused a dose
-dependent increase in [Ca2+](i) in Jurkat cells which was blunted maximall
y with 0.6 mM glycine. The effect of glycine was dependent on extracellular
chloride and reversed by strychnine, an antagonist of the glycine-gated ch
loride channel. Similar results were obtained with rat T lymphocytes stimul
ated by anti-CD3 Ab, Surprisingly, glycine had no effect on IL-2 production
in the mixed lymphocyte culture; therefore, the effect of glycine on IL-2-
dependent proliferation was tested. Glycine and rapamycin caused dose-depen
dent decreases in IL-2-stimulated growth of CtlI-2 cells to about 60% and 4
0%, respectively, of control. Moreover, glycine also inhibited the IL-2-sti
mulated growth of rat splenic lymphocytes. It is concluded that glycine blu
nts proliferation in an IL-2-independent manner. This is consistent with th
e hypothesis that glycine activates a glycine-gated chloride channel and hy
perpolarizes the cell membrane-blunting increases in [Ca2+](i) that are req
uired for transcription of factors necessary for cell proliferation.