Cytokines secreted by IL-2-activated lymphocytes induce endogenous nitric oxide synthesis and apoptosis in macrophages

  • Kyoung Seong Choi
  • , Eun Kee Song
  • , Chang Yeol Yim*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

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 languageEnglish
Pages (from-to)1440-1450
Number of pages11
JournalJournal of Leukocyte Biology
Volume83
Issue number6
DOIs
StatePublished - 2008.06.1

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    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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