A neurotoxic phospholipase A2 impairs yeast amphiphysin activity and reduces endocytosis

PLoS One. 2012;7(7):e40931. doi: 10.1371/journal.pone.0040931. Epub 2012 Jul 23.

Abstract

Background: Presynaptically neurotoxic phospholipases A(2) inhibit synaptic vesicle recycling through endocytosis.

Principal findings: Here we provide insight into the action of a presynaptically neurotoxic phospholipase A(2) ammodytoxin A (AtxA) on clathrin-dependent endocytosis in budding yeast. AtxA caused changes in the dynamics of vesicle formation and scission from the plasma membrane in a phospholipase activity dependent manner. Our data, based on synthetic dosage lethality screen and the analysis of the dynamics of sites of endocytosis, indicate that AtxA impairs the activity of amphiphysin.

Conclusions: We identified amphiphysin and endocytosis as the target of AtxA intracellular activity. We propose that AtxA reduces endocytosis following a mechanism of action which includes both a specific protein-protein interaction and enzymatic activity, and which is applicable to yeast and mammalian cells. Knowing how neurotoxic phospholipases A(2) work can open new ways to regulate endocytosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins / metabolism
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cytoskeletal Proteins / antagonists & inhibitors*
  • Endocytosis / drug effects*
  • Endocytosis / genetics
  • Genomics
  • Microfilament Proteins / antagonists & inhibitors*
  • Nerve Tissue Proteins / antagonists & inhibitors*
  • Neurotoxins / toxicity*
  • Phospholipases A2 / toxicity*
  • Phospholipids / metabolism
  • Saccharomyces cerevisiae Proteins / antagonists & inhibitors*
  • Saccharomyces cerevisiae Proteins / metabolism
  • Transport Vesicles / drug effects
  • Transport Vesicles / metabolism

Substances

  • 14-3-3 Proteins
  • BMH1 protein, S cerevisiae
  • BMH2 protein, S cerevisiae
  • Cytoskeletal Proteins
  • Microfilament Proteins
  • Nerve Tissue Proteins
  • Neurotoxins
  • Phospholipids
  • RVS161 protein, S cerevisiae
  • RVS167 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • amphiphysin
  • Phospholipases A2