BMB Reports (Feb 2012)

CopA3 peptide from Copris tripartitus induces apoptosis in human leukemia cells via a caspase-independent pathway

  • Bo Ram Kang,
  • Ho Kim,
  • Sung-Hee Nam,
  • Eun-Young Yun,
  • Seong-Ryul Kim,
  • Mi-Young Ahn,
  • Jong Soo Chang,
  • Jae Sam Hwang

DOI
https://doi.org/10.5483/BMBRep.2012.45.2.85
Journal volume & issue
Vol. 45, no. 2
pp. 85 – 90

Abstract

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Our previous study demonstrated that CopA3, a disulfide dimerof the coprisin peptide analogue (LLCIALRKK), has antibacterialactivity. In this study, we assessed whether CopA3caused cellular toxicity in various mammalian cell lines.CopA3 selectively caused a marked decrease in cell viabilityin Jurkat T, U937, and AML-2 cells (human leukemia cells),but was not cytotoxic to Caki or Hela cells. Fragmentation ofDNA, a marker of apoptosis, was also confirmed in the leukemiacell lines, but not in the other cells. CopA3-induced apoptosisin leukemia cells was mediated by apoptosis inducingfactor (AIF), indicating induction of a caspase-independent signalingpathway. [BMB reports 2012; 45(2): 85-90]

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