Manipulation of NK cytotoxicity by the IAP family member Livin

Boaz Nachmias, Sa'ar Mizrahi, Meital Elmalech, Itay Lazar, Yaqoub Ashhab, Roi Gazit, Gal Markel, Dina Ben-Yehuda, Ofer Mandelboim*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


Natural killer (NK) cells are part of the innate immune system, capable of killing tumor and virally infected cells. NK cells induce apoptosis in the target cell by either granule- or receptor-mediated pathways. A set of inhibitory and activation ligands governs NK cell activation. As transformed cells often attempt to evade NK cell killing, up-regulation of a potential anti-apoptotic factor should provide a survival advantage. The inhibitor of apoptosis protein (IAP) family can inhibit apoptosis induced by a variety of stimuli. We have previously described a new IAP family member, termed Livin, which has two splice variants (α and β) with differential anti-apoptotic activities. In this study, we explore the ability of Livin to inhibit NK cell-induced killing. We demonstrate that Livin β moderately protects against NK cell killing whereas Livin α augments killing. We show that Livin β inhibition in Jurkat cells is apparent upon concomitant activation of an inhibitory signal, suggesting that Livin augments an extrinsic inhibitory signal rather than functioning as an independent inhibitory mechanism. Finally, we demonstrate that detection of both Livin isoforms in melanoma cells correlates with a low killing rate. To date, this is the first evidence that directly demonstrates the ability of IAP to protect against NK cell-induced apoptosis.

Original languageAmerican English
Pages (from-to)3467-3476
Number of pages10
JournalEuropean Journal of Immunology
Issue number12
StatePublished - Dec 2007


  • Apoptosis
  • Cancer
  • IAP
  • Livin
  • NK cells


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