4.5 Article

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

Journal

BIOCHEMICAL JOURNAL
Volume 475, Issue -, Pages 1385-1396

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/BCJ20170894

Keywords

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Funding

  1. National Natural Science Foundation of China [31071922, 31572264]
  2. Fundamental Research Funds for Henan Provincial Colleges and Universities in Henan University of Technology [2015RCJH03]
  3. Henan Provincial Science and Technology Research Project [162102310404]
  4. National Engineering Laboratory for Wheat & Corn Further Processing, Henan University of Technology [NL2016010]

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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.

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