Role of calcium in reactive oxygen species-induced apoptosis in Candida albicans: an antifungal mechanism of antimicrobial peptide, PMAP-23

References

• Kim J-Y, Park S-C, Yoon M-Y, et al. C-terminal amidation of PMAP-23: translocation to the inner membrane of Gram-negative bacteria. Amino Acids. 2011;40:183–195.
   PubMed Web of Science ®Google Scholar
• Brown KL, Hancock RE. Cationic host defense (antimicrobial) peptides. Curr Opin Immunol. 2006;18:24–30.
   PubMed Web of Science ®Google Scholar
• Rautenbach M, Troskie AM, Vosloo JA. Antifungal peptides: to be or not to be membrane active. Biochimie. 2016;130:132–145.
   PubMed Web of Science ®Google Scholar
• Bechinger B, Gorr SU. Antimicrobial peptides: mechanisms of action and resistance. J Dent Res. 2017;96:254–260.
   PubMed Web of Science ®Google Scholar
• Park SC, Park Y, Hahm KS. The role of antimicrobial peptides in preventing multidrug-resistant bacterial infections and biofilm formation. IJMS. 2011;12:5971–5992.
   Google Scholar
• Ciociola T, Giovati L, Conti S, et al. Natural and synthetic peptides with antifungal activity. Future Med Chem. 2016;8:1413–1433.
   PubMed Web of Science ®Google Scholar
• Marcos JF, Gandía M. Antimicrobial peptides: to membranes and beyond. Expert Opin Drug Discov. 2009;4:659–671.
   PubMed Web of Science ®Google Scholar
• Yang S-T, Jeon J-H, Kim Y, et al. Possible role of a PXXP central hinge in the antibacterial activity and membrane interaction of PMAP-23, a member of cathelicidin family. Biochemistry. 2006;45:1775–1784.
   PubMed Web of Science ®Google Scholar
• Morton CO, Dos Santos SC, Coote P. An amphibian-derived, cationic, α-helical antimicrobial peptide kills yeast by caspase-independent but AiF-dependent programmed cell death. Mol Microbiol. 2007;65:494–507.
   PubMed Web of Science ®Google Scholar
• Muñoz A, López-García B, Marcos JF. Studies on the mode of action of the antifungal hexapeptide PAF26. Antimicrob Agents Chemother. 2006;50:3847–3855.
   PubMed Web of Science ®Google Scholar
• Yun J, Lee DG. Cecropin A-induced apoptosis is regulated by ion balance and glutathione antioxidant system in Candida albicans. IUBMB Life. 2016;68:652–662.
   PubMed Web of Science ®Google Scholar
• Kohanski MA, Dwyer DJ, Hayete B, et al. A common mechanism of cellular death induced by bactericidal antibiotics. Cell. Cell. 2007;130:797–810.
   PubMed Web of Science ®Google Scholar
• Hu BH, Zheng GL. Membrane disruption: an early event of hair cell apoptosis induced by exposure to intense noise. Brain Res. 2008;1239:107–118.
   PubMed Web of Science ®Google Scholar
• Lee DG, Kim D-H, Park Y, et al. Fungicidal effect of antimicrobial peptide, PMAP-23, isolated from porcine myeloid against Candida albicans. Biochem Biophys Res Commun. 2001;282:570–574.
   PubMed Web of Science ®Google Scholar
• Rodrigues A, Fonseca A, Sansonetty F, et al. Antifungal activity of ibuprofen alone and in combination with fluconazole against Candida species. J Med Microbiol. 2000;49:831–840.
   PubMed Web of Science ®Google Scholar
• Yu SP. Regulation and critical role of potassium homeostasis in apoptosis. Prog Neurobiol. 2003;70:363–386.
   PubMed Web of Science ®Google Scholar
• Massudi H, Grant R, Guillemin GJ, et al. NAD + metabolism and oxidative stress: the golden nucleotide on a crown of thorns. Redox Rep. 2012;17:28–46.
   PubMed Web of Science ®Google Scholar
• Heux S, Cachon R, Dequin S. Cofactor engineering in Saccharomyces cerevisiae: expression of a H2O-forming NADH oxidase and impact on redox metabolism. Metab Eng. 2006;8:303–314.
   PubMed Web of Science ®Google Scholar
• Lupetti A, Brouwer CPJM, Dogterom-Ballering HEC, et al. Release of calcium from intracellular stores and subsequent uptake by mitochondria are essential for the candidacidal activity of an N-terminal peptide of human lactoferrin. J Antimicrob Chemother. 2004;54:603–608.
   PubMed Web of Science ®Google Scholar
• Gonçalves AP, Cordeiro JM, Monteiro J, et al. Involvement of mitochondrial proteins in calcium signaling and cell death induced by staurosporine in Neurospora crassa. Biochim Biophys Acta. 2015;1847:1064–1074.
   PubMed Web of Science ®Google Scholar
• Diaz-Vivancos P, de Simone A, Kiddle G, et al. Glutathione-linking cell proliferation to oxidative stress. Free Radic Biol Med. 2015;89:1154–1164.
   PubMed Web of Science ®Google Scholar
• Lee W, Lee DG. Reactive oxygen species modulate itraconazole-induced apoptosis via mitochondrial disruption in Candida albicans. Free Radic Res. 2018;52:39–50.
   PubMed Web of Science ®Google Scholar
• Yun J, Lee DG. A novel fungal killing mechanism of propionic acid. FEMS Yeast Res. 2016;16:fow089.
   PubMed Web of Science ®Google Scholar
• Elmore S. Apoptosis: a review of programmed cell death. Toxicol Pathol. 2007;35:495–516.
   PubMed Web of Science ®Google Scholar
• Bahar AA, Ren D. Antimicrobial peptides. Pharmaceuticals. 2013;6:1543–1575.
   Google Scholar
• Viejo-Díaz M, Andrés MT, Fierro JF. Modulation of in vitro fungicidal activity of human lactoferrin against Candida albicans by extracellular cation concentration and target cell metabolic activity. Antimicrob Agents Chemother. 2004;48:1242–1248.
   PubMed Web of Science ®Google Scholar
• Orioni B, Bocchinfuso G, Kim JY, et al. Membrane perturbation by the antimicrobial peptide PMAP-23: a fluorescence and molecular dynamics study. Biochim Biophys Acta. 2009;1788:1523–1533.
   PubMed Web of Science ®Google Scholar
• Veldhuizen EJA, Scheenstra MR, Tjeerdsma-van Bokhoven JLM, et al. Antimicrobial and immunomodulatory activity of pmap-23 derived peptides. Protein Pept Lett. 2017;24:609–616.
   PubMed Web of Science ®Google Scholar
• Muñoz A, Chu M, Marris PI, et al. Specific domains of plant defensins differentially disrupt colony initiation, cell fusion and calcium homeostasis in Neurospora crassa. Mol Microbiol. 2014;92:1357–1374.
   PubMed Web of Science ®Google Scholar
• Lee W, Lee DG. A novel mechanism of fluconazole: fungicidal activity through dose-dependent apoptotic responses in Candida albicans. Microbiology. 2018;164:194–204.
   PubMed Web of Science ®Google Scholar
• Courchesne WE, Tunc M, Liao S. Amiodarone induces stress responses and calcium flux mediated by the cell wall in Saccharomyces cerevisiae. Can J Microbiol. 2009;55:288–303.
   PubMed Web of Science ®Google Scholar
• Liu S, Hou Y, Liu W, et al. Components of the calcium-calcineurin signaling pathway in fungal cells and their potential as antifungal targets. Eukaryot Cell. 2015;14:324–334.
   PubMedGoogle Scholar
• Griffiths EJ, Rutter GA. Mitochondrial calcium as a key regulator of mitochondrial ATP production in mammalian cells. Biochim Biophys Acta. 2009;1787:1324–1333.
   PubMed Web of Science ®Google Scholar
• Orrenius S, Zhivotovsky B, Nicotera P. Regulation of cell death: the calcium-apoptosis link. Nat Rev Mol Cell Biol. 2003;4:552–565.
   PubMed Web of Science ®Google Scholar
• Pan L, Xu L, Zhao X, et al. Mechanism underlying mitochondrial protection of Asiatic acid against hepatotoxicity in mice. J Pharm Pharmacol. 2006;58:227–233.
   PubMed Web of Science ®Google Scholar
• Marcu R, Wiczer BM, Neeley CK, et al. Mitochondrial matrix Ca2+ accumulation regulates cytosolic NAD+/NADH metabolism, protein acetylation, and sirtuin expression. Mol Cell Biol. 2014;34:2890–2902.
   PubMed Web of Science ®Google Scholar
• Fang J, Beattie DS. External alternative NADH dehydrogenase of Saccharomyces cerevisiae: a potential source of superoxide. Free Radic Biol Med. 2003;34:478–488.
   PubMed Web of Science ®Google Scholar
• Farrugia G, Balzan R. Oxidative stress and programmed cell death in yeast. Front Oncol. 2012;2:64.
   PubMedGoogle Scholar
• Ren T, Zhang H, Wang J, et al. MCU-dependent mitochondrial Ca2+ inhibits NAD+/SIRT3/SOD2 pathway to promote ROS production and metastasis of HCC cells. Oncogene. 2017;36:5897–5909.
   PubMed Web of Science ®Google Scholar
• Chiu J, Dawes IW. Redox control of cell proliferation. Trends Cell Biol. 2012;22:592–601.
   PubMed Web of Science ®Google Scholar