C2-phytoceramide perturbs lipid rafts and cell integrity in Saccharomyces cerevisiae in a sterol-dependent manner

PLoS One. 2013 Sep 11;8(9):e74240. doi: 10.1371/journal.pone.0074240. eCollection 2013.

Abstract

Specific ceramides are key regulators of cell fate, and extensive studies aimed to develop therapies based on ceramide-induced cell death. However, the mechanisms regulating ceramide cytotoxicity are not yet fully elucidated. Since ceramides also regulate growth and stress responses in yeast, we studied how different exogenous ceramides affect yeast cells. C2-phytoceramide, a soluble form of phytoceramides, the yeast counterparts of mammalian ceramides, greatly reduced clonogenic survival, particularly in the G2/M phase, but did not induce autophagy nor increase apoptotic markers. Rather, the loss of clonogenic survival was associated with PI positive staining, disorganization of lipid rafts and cell wall weakening. Sensitivity to C2-phytoceramide was exacerbated in mutants lacking Hog1p, the MAP kinase homolog of human p38 kinase. Decreasing sterol membrane content reduced sensitivity to C2-phytoceramide, suggesting sterols are the targets of this compound. This study identified a new function of C2-phytoceramide through disorganization of lipid rafts and induction of a necrotic cell death under hypo-osmotic conditions. Since lipid rafts are important in mammalian cell signaling and adhesion, our findings further support pursuing the exploitation of yeast to understand the basis of synthetic ceramides' cytotoxicity to provide novel strategies for therapeutic intervention in cancer and other diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Death / drug effects
  • Cell Survival / drug effects
  • Cell Wall / chemistry
  • Cell Wall / drug effects*
  • Ergosterol / chemistry
  • Ergosterol / metabolism*
  • G2 Phase Cell Cycle Checkpoints / drug effects
  • Gene Expression
  • Humans
  • Membrane Microdomains / chemistry
  • Membrane Microdomains / drug effects*
  • Mitogen-Activated Protein Kinases / deficiency
  • Mitogen-Activated Protein Kinases / genetics
  • Saccharomyces cerevisiae / chemistry
  • Saccharomyces cerevisiae / drug effects*
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae Proteins / genetics
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • Sphingosine / analogs & derivatives*
  • Sphingosine / pharmacology
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • N-acetylsphingosine
  • Saccharomyces cerevisiae Proteins
  • HOG1 protein, S cerevisiae
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Sphingosine
  • Ergosterol

Grants and funding

This work was supported by Fundação para a Ciência e Tecnologia through projects PTDC/BIA-BCM/69448/2006 and PEst-C/BIA/UI4050/2011, and fellowships to A.P. (SFRH/BPD/65003) and F.A. (SFRH/BD/80934/2011), as well as by FEDER through POFC – COMPETE. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.