CGA-N12, a peptide derived from chromogranin A, promotes apoptosis of Candida tropicalis by attenuating mitochondrial functions

Biochem J. 2018 Apr 16;475(7):1385-1396. doi: 10.1042/BCJ20170894.

Abstract

CGA-N12 (the amino acid sequence from the 65th to the 76th residue of the N-terminus of chromagranin A) is an antifungal peptide derived from human chromogranin A (CGA). In our previous investigation, CGA-N12 was found to have specific anti-candidal activity, though the mechanism of action remained unclear. Here, we investigated the effects of CGA-N12 on mitochondria. We found that CGA-N12 induced an over-generation of intracellular reactive oxygen species and dissipation in mitochondrial membrane potential, in which the former plays key roles in the initiation of apoptosis and the latter is a sign of the cell apoptosis. Accordingly, we assessed the apoptosis features of Candida tropicalis cells after treatment with CGA-N12 and found the following: leakage of cytochrome c and uptake of calcium ions into mitochondria and the cytosol; metacaspase activation; and apoptotic phenotypes, such as chromatin condensation and DNA degradation. In conclusion, CGA-N12 is capable of inducing apoptosis in C. tropicalis cells through mitochondrial dysfunction and metacaspase activation. Antifungal peptide CGA-N12 from human CGA exhibits a novel apoptotic mechanism as an antifungal agent.

Keywords: CGA-N12; antifungal peptide; cytochrome c; metacaspase activation; mitochondrial membrane potential; yeast apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Calcium / metabolism
  • Candida tropicalis / drug effects*
  • Candida tropicalis / growth & development
  • Candida tropicalis / metabolism
  • Chromogranin A / metabolism*
  • Cytochromes c / metabolism
  • Cytosol / metabolism
  • Humans
  • Membrane Potential, Mitochondrial / drug effects*
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / pathology*
  • Peptide Fragments / pharmacology*
  • Reactive Oxygen Species / metabolism

Substances

  • CHGA protein, human
  • Chromogranin A
  • Peptide Fragments
  • Reactive Oxygen Species
  • Cytochromes c
  • Calcium