Inositol phosphosphingolipid phospholipase C1 regulates plasma membrane ATPase (Pma1) stability in Cryptococcus neoformans

FEBS Lett. 2014 Nov 3;588(21):3932-8. doi: 10.1016/j.febslet.2014.09.005. Epub 2014 Sep 18.

Abstract

Cryptococcus neoformans is a facultative intracellular pathogen, which can replicate in the acidic environment inside phagolysosomes. Deletion of the enzyme inositol-phosphosphingolipid-phospholipase-C (Isc1) makes C. neoformans hypersensitive to acidic pH likely by inhibiting the function of the proton pump, plasma membrane ATPase (Pma1). In this work, we examined the role of Isc1 on Pma1 transport and oligomerization. Our studies showed that Isc1 deletion did not affect Pma1 synthesis or transport, but significantly inhibited Pma1 oligomerization. Interestingly, Pma1 oligomerization could be restored by supplementing the medium with phytoceramide. These results offer insight into the mechanism of intracellular survival of C. neoformans.

Keywords: Cryptococcus neoformans; Inositiol phosphosphingolipid phospholipase C (Isc1); Plasma membrane; Plasma membrane ATPase (Pma1); Sphingolipid.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphatases / biosynthesis
  • Adenosine Triphosphatases / chemistry*
  • Adenosine Triphosphatases / metabolism*
  • Cell Membrane / drug effects
  • Cell Membrane / enzymology*
  • Ceramides / pharmacology
  • Cryptococcus neoformans / cytology
  • Cryptococcus neoformans / enzymology*
  • Cryptococcus neoformans / genetics
  • Cryptococcus neoformans / physiology
  • Enzyme Stability
  • Gene Deletion
  • Intracellular Space / microbiology
  • Protein Multimerization / drug effects
  • Protein Structure, Quaternary
  • Protein Transport / drug effects
  • Type C Phospholipases / deficiency
  • Type C Phospholipases / genetics
  • Type C Phospholipases / metabolism*

Substances

  • Ceramides
  • Type C Phospholipases
  • Adenosine Triphosphatases