Abstract
IL-2-activated killer (LAK) cells secrete inflammatory cytokines such as IFN-γ and TNF-α, which can induce NO synthesis (NOS). In this study, we investigated IL-2-activated lymphocyte-mediated macrophage apoptosis via NOS. LAK cells and their culture supernatants induced NOS in murine macrophages. NOS was markedly inhibited by blocking antibodies to IFN-γ and TNF-α, suggesting the key role of these lymphocyte cytokines in mediating NOS. Endogenous NO production inhibited macrophage proliferation and induced apoptosis in concordance with p53 accumulation and caspase-3 activation, processes that were inhibited by NG-monomethyl-L-arginine (a NOS inhibitor) and 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide (a NO scavenger). Our study demonstrated a novel, noncontact-dependent mechanism of macrophage suppression by IL-2-activated lymphocytes: induction of growth inhibition and apoptosis of macrophages as a result of endogenous NOS induced by cytokines secreted from IL-2-activated lymphocytes.
| Original language | English |
|---|---|
| Pages (from-to) | 1440-1450 |
| Number of pages | 11 |
| Journal | Journal of Leukocyte Biology |
| Volume | 83 |
| Issue number | 6 |
| DOIs | |
| State | Published - 2008.06.1 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Carboxy-PTIO
- Caspase-3
- iNOS
- p53
- Programmed cell death
- SNAP
Quacquarelli Symonds(QS) Subject Topics
- Medicine
- Biological Sciences
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