Decay accelerating factor regulates complement activation on glomerular epithelial cells

J Immunol. 1989 Feb 1;142(3):877-82.

Abstract

Epithelial cells of the glomerular capillary are the site of C5b-9 mediated injury in rat membranous nephropathy. We investigated the regulation of C activation by cultured glomerular epithelial cells (GEC). Rat and human GEC were more resistant to C injury by homologous C than heterologous C. In human GEC homologous C cytotoxicity was enhanced by antiserum to decay accelerating factor (DAF) indicating that homologous C activation was, at least in part, restricted by membrane DAF. Anti-DAF immunoprecipitated a 67-kDa protein from human glomeruli. In rat GEC, pronase and phosphatidylinositol-specific phospholipase C (which are known to inactivate human DAF) enhanced cytotoxicity by homologous C. Thus, DAF is present on human GEC in culture and in human kidney glomeruli, and a DAF-like protein is present on cultured rat GEC. These proteins regulate C activation in vitro and may play a role in controlling C activation on GEC in vivo.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • CD55 Antigens
  • Cells, Cultured
  • Complement Activation* / drug effects
  • Complement C8 / immunology
  • Complement C9 / immunology
  • Complement Inactivator Proteins / physiology*
  • Cytotoxicity, Immunologic
  • Edetic Acid
  • Epithelium / immunology
  • Guinea Pigs
  • Humans
  • Kidney Glomerulus / immunology*
  • Membrane Proteins / physiology*
  • Rabbits
  • Rats

Substances

  • CD55 Antigens
  • Complement C8
  • Complement C9
  • Complement Inactivator Proteins
  • Membrane Proteins
  • Edetic Acid