Glycine inhibits growth of T lymphocytes by an IL-2-independent mechanism

Citation
Rf. Stachlewitz et al., Glycine inhibits growth of T lymphocytes by an IL-2-independent mechanism, J IMMUNOL, 164(1), 2000, pp. 176-182
Citations number
38
Categorie Soggetti
Immunology
Journal title
JOURNAL OF IMMUNOLOGY
ISSN journal
00221767 → ACNP
Volume
164
Issue
1
Year of publication
2000
Pages
176 - 182
Database
ISI
SICI code
0022-1767(20000101)164:1<176:GIGOTL>2.0.ZU;2-X
Abstract
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.