Ca2+-activated K+ efflux limits complement-mediated lysis of human erythrocytes

J Clin Invest. 1989 May;83(5):1466-71. doi: 10.1172/JCI114039.

Abstract

The lytic effect of complement on human erythrocytes has been reported by others to increase when Na+ is substituted for K+ in the external medium. In this paper we have investigated the hypothesis that net loss of K+ through a K+ transport pathway protects erythrocytes from complement-induced colloidosmotic swelling and lysis. Antibody-sensitized human erythrocytes containing different intracellular cation concentrations (nystatin treatment) were exposed to low concentrations of guinea pig serum in media of different cation composition; complement lysis was assessed by the release of hemoglobin and the volume of the surviving cells estimated by their density distribution profiles. Complement-dependent swelling and lysis of erythrocytes (a) were limited by the presence of an outwardly directed K+ electrochemical gradient and (b) were enhanced by carbocyanine, a specific inhibitor of the Ca2+-activated K+ transport pathway, and by absence of Ca2+ in the external medium. We propose that during complement activation a rising cytosolic calcium triggers the Ca2+-activated K+ permeability pathway, the Gardos effect, produces a net K+, Cl- and water loss, and thus limits the colloidosmotic swelling and lysis of erythrocytes.

Publication types

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

MeSH terms

  • Animals
  • Biological Transport
  • Calcium / physiology*
  • Cell Membrane Permeability
  • Colloids
  • Complement Activation*
  • Electrochemistry
  • Erythrocyte Membrane / physiology*
  • Guinea Pigs
  • Hemolysis*
  • Humans
  • Hypotonic Solutions
  • Osmotic Pressure
  • Potassium Channels / physiology*
  • Potassium Chloride
  • Sodium Chloride

Substances

  • Colloids
  • Hypotonic Solutions
  • Potassium Channels
  • Sodium Chloride
  • Potassium Chloride
  • Calcium