Dichotomy of glutathione regulation of the activation of resting and preactivated lymphocytes
| Autor: | Susan O. Sharrow, Shu-Mei Liang, Chi-Ming Liang, Myrthel E. Hargrove, Chou-Chik Ting |
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| Rok vydání: | 1992 |
| Předmět: |
Antigens
Differentiation T-Lymphocyte Interleukin 2 Time Factors CD3 Complex Transcription Genetic Lymphocyte T cell CD3 Immunology Genes myc Receptors Antigen T-Cell chemical and pharmacologic phenomena Biology Lymphocyte Activation Mice T-Lymphocyte Subsets Methionine Sulfoximine medicine Animals Cytotoxic T cell Killer Cells Lymphokine-Activated Receptor Buthionine Sulfoximine Mercaptoethanol Lymphokine-activated killer cell Lymphokine Glutathione Cell biology Mice Inbred C57BL medicine.anatomical_structure Biochemistry biology.protein Interleukin-2 Female medicine.drug |
| Zdroj: | Cellular Immunology. 142:40-53 |
| ISSN: | 0008-8749 |
| DOI: | 10.1016/0008-8749(92)90267-s |
| Popis: | The present study has examined the effect of GSH on two lines of IL-2-dependent activated killer cells, LAK cells and alpha CD3-activated killer (CD3-AK) cells. We found that GSH added during first 24 hr decreased the generation of LAK and CD3-AK cells from resting lymphocytes, whereas after 48 hr of activation, the addition of GSH increased the killer cell activity. In addition, BSO, an inhibitor of GSH biosynthesis, decreased the proliferation and cytotoxic activities of activated killer cells, and the inhibitory effect was reversed by GSH. These results indicate that GSH downregulates the generation of LAK or CD3-AK cells from resting lymphocytes, but it upregulates the further differentiation of preactivated killer cells. The effect of GSH thus varied with the state of activation of the killer cells. Culturing CD3-AK cells in GSH did not change the distribution of T cell subsets, did not affect the cells' ability to produce lymphokine (IL-2), and did not induce suppressor cells. One striking change as revealed by flow cytometry analysis was that the levels of IL-2 receptor and TCR (alpha/beta)-CD3 were reduced by 80 and 30%, respectively, after 48 hr culturing in GSH. Determination of the mRNA of IL-2 receptor suggests that a post-transcriptional block existed. It appears that the negative effect of GSH on the function of surface IL-2 receptors or T cell receptors on resting lymphocytes severely affected the signal transduction through these receptors and thus abrogated or reduced LAK or CD3-AK cell response. In contrast, for preactivated killer cells, upregulation by intracellular GSH of IL-2 utilization is a dominant effect, thus allowing further differentiation of these killer cells. Our results indicate that the balance between the activation signal (IL-2 or alpha CD3) and the immunoregulatory signal (induced by GSH) may determine the outcome of the immune response. |
| Databáze: | OpenAIRE |
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