| Autor: |
Grove, Deborah S., Crowl, Caren V., Gagajewski, Angelique, Yang, Chung-Shi, Reddy, Gongiti Ravindra, Hamilton, Gordon A., Mastro, Andrea M. |
| Zdroj: |
Experimental Cell Research; May 1996, Vol. 225 Issue: 1 p162-170, 9p |
| Abstrakt: |
Previously we have shown thatS-oxalins (monothiolesters of oxalic acid) are ubiquitous mammalian metabolites whose concentrations decrease when lymphocytes are stimulated to proliferate. The present study was undertaken to further examine the role ofS-oxalins in the proliferation process. When added to lymphocytes stimulated with concanavalin A, theS-oxalin,S-oxalylglutathione (GS-Ox), inhibited DNA synthesis by 50% when present at ca. 0.15 mMand virtually 100% at 0.5 mM.The inhibition was reversible. The presence of GS-Ox blocked IL-2 production, but addition of IL-2 did not permit DNA synthesis to proceed. GS-Ox also inhibited proliferation of an IL-2-dependent cell line, BT2. In primary lymphocytes GS-Ox reduced IL-2 receptor expression, but not in an IL-2-dependent blast cell line. Overall RNA synthesis and protein synthesis were not significantly altered by GS-Ox. Levels of the positive transcription factor, NF-κB, were decreased after incubation of lymphocytes with GS-Ox, but the amount of a negative transcription factor, NREA, was largely unchanged. The results not only provide further evidence thatS-oxalins are small-molecule cell proliferation inhibitors, they also clarify to some extent the specific steps in the activation response modulated byS-oxalins. |
| Databáze: |
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