Phagocytosis of P. falciparum malarial pigment hemozoin by human monocytes inactivates monocyte protein kinase C

Biochim Biophys Acta. 1993 Mar 24;1181(1):51-4. doi: 10.1016/0925-4439(93)90089-j.

Abstract

Hemozoin (malarial pigment) is a ferriprotoporphyrin IX-rich hemoglobin degradation product present in parasitized RBC. Avidly phagocytosed hemozoin abolishes phagocyte TPA-induced oxidative burst. Membrane-associated PKC increased transiently in hemozoin-fed monocytes by 50% after 30 min and decreased irreversibly to 20% of initial value within 5 h after phagocytosis. Control RBC-fed monocytes showed transient decay of membrane-associated PKC followed by complete recovery 12 h after phagocytosis. Cytosolic PKC was not impaired within 12 h and diminished drastically 24 h after phagocytosis of hemozoin. Results are compatible with increased degradation of membrane-translocated PKC, possibly by iron/H2O2-mediated damage of cysteine-rich regulatory domains of PKC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Hemeproteins / metabolism*
  • Hemeproteins / pharmacology
  • Humans
  • Monocytes / drug effects
  • Monocytes / enzymology*
  • Monocytes / immunology
  • Phagocytosis*
  • Pigments, Biological / metabolism*
  • Pigments, Biological / pharmacology
  • Plasmodium falciparum / immunology*
  • Plasmodium falciparum / metabolism
  • Protein Kinase C / antagonists & inhibitors*
  • Respiratory Burst

Substances

  • Hemeproteins
  • Pigments, Biological
  • hemozoin
  • Protein Kinase C