Release of arachidonic acid by complement C5b-9 complex in glomerular epithelial cells

Am J Physiol. 1991 Sep;261(3 Pt 2):F427-36. doi: 10.1152/ajprenal.1991.261.3.F427.

Abstract

In experimental membranous nephropathy, C5b-9 induces noncytolytic glomerular epithelial cell (GEC) injury and proteinuria, which in some models is partially mediated by metabolites of arachidonic acid. In cultured GEC, sublytic C5b-9 increases cytosolic Ca2+ concentration ([Ca2+]i), activates phospholipase C (PLC), and releases arachidonic acid and eicosanoids. This study examined mechanisms of arachidonic acid production by C5b-9. In GEC labeled with [3H]arachidonate C5b-9 increased free [3H]arachidonic acid and 1,2-[3H]-arachidonoyl-diacylglycerol (DAG), an endogenous activator of protein kinase C (PKC). Elevated [Ca2+]i was not sufficient to account for increased free arachidonic acid. Moreover, in GEC that had been depleted of PKC by preincubation for 18 h with 2 microM phorbol myristate acetate, the C5b-9-induced arachidonate release was inhibited by greater than 75%. Reacylation of phospholipids was not decreased by C5b-9. Homogenates of GEC that had been stimulated with C5b-9 released more [14C]arachidonate from exogenously added 2-[14C]arachidonoyl-phosphatidyl-ethanolamine or 2-[14C]arachidonoyl-phosphatidylcholine than homogenates of unstimulated cells (assayed at a Ca2+ concentration of 2 mM). These experiments demonstrate directly that C5b-9 increased phospholipase A2 (PLA2) activity. PLA2 appeared to be stimulated as a result of PKC activation (probably secondary to increased DAG) in association with elevated [Ca2+]i. The C5b-9-induced activation of PLA2 may lead to release of eicosanoids, which may contribute toward impaired glomerular capillary wall permselectivity in experimental membranous nephropathy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonic Acid
  • Arachidonic Acids / metabolism*
  • Calcimycin / analogs & derivatives
  • Calcimycin / pharmacology
  • Calcium / metabolism
  • Cells, Cultured
  • Complement Membrane Attack Complex / pharmacology*
  • Cyclohexanones / pharmacology
  • Diglycerides / metabolism
  • Diglycerides / pharmacology
  • Edetic Acid / pharmacology
  • Egtazic Acid / pharmacology
  • Epithelium / drug effects
  • Epithelium / physiology
  • Fatty Acids, Nonesterified / metabolism
  • Kidney Glomerulus / drug effects
  • Kidney Glomerulus / physiology*
  • Kinetics
  • Lipase / metabolism
  • Lipoprotein Lipase / antagonists & inhibitors
  • Phospholipases A / metabolism
  • Phospholipases A2
  • Phospholipids / biosynthesis
  • Protein Kinase C / metabolism
  • Rats
  • Tetradecanoylphorbol Acetate / pharmacology

Substances

  • Arachidonic Acids
  • Complement Membrane Attack Complex
  • Cyclohexanones
  • Diglycerides
  • Fatty Acids, Nonesterified
  • Phospholipids
  • Arachidonic Acid
  • Calcimycin
  • Egtazic Acid
  • 1,6-bis(cyclohexyloximinocarbonyl)hexane
  • 1-oleoyl-2-acetylglycerol
  • Edetic Acid
  • Protein Kinase C
  • Lipase
  • Phospholipases A
  • Lipoprotein Lipase
  • Phospholipases A2
  • Tetradecanoylphorbol Acetate
  • Calcium