Beta(2)-glycoprotein I promotes the binding of anionic phospholipid vesicles by macrophages

Arterioscler Thromb Vasc Biol. 1999 Nov;19(11):2807-11. doi: 10.1161/01.atv.19.11.2807.

Abstract

Beta(2)-Glycoprotein I is a single-chain 50-kDa protein that circulates in plasma at a concentration of approximately 200 microg/mL. Its physiological role remains uncertain, but an important clue is the frequent presence of antibodies to this protein in patients with recurrent thrombosis. We have isolated beta(2)-glycoprotein I and examined its effect on the binding of phosphatidylserine (PS) vesicles by human monocyte-derived macrophages and by phorbol ester-stimulated THP-1 cells. beta(2)-Glycoprotein I stimulated the binding of PS vesicles by these cells in a concentration-dependent manner. Vesicles containing other anionic phospholipids, such as cardiolipin, phosphatidic acid, or cardiolipin, inhibited the binding, whereas PC vesicles had no effect. Platelet-derived microvesicles, which contain anionic phospholipid on the outer leaflet of their phospholipid bilayer, also inhibited beta(2)-glycoprotein I-dependent binding of anionic phospholipid vesicles. The binding is associated with incorporation of phospholipid in the cell membrane and internalization of beta(2)-glycoprotein I. These findings suggest a physiological function for beta(2)-glycoprotein I in the clearance of procoagulant anionic phospholipid-containing cell surfaces from the circulation.

Publication types

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

MeSH terms

  • Anions / metabolism
  • Cardiolipins / metabolism
  • Cells, Cultured
  • Cholesterol / metabolism
  • Endocytosis / physiology
  • Flow Cytometry
  • Glycoproteins / isolation & purification
  • Glycoproteins / metabolism*
  • Glycoproteins / pharmacology*
  • Humans
  • Lupus Coagulation Inhibitor / metabolism
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Membrane Glycoproteins / isolation & purification
  • Membrane Glycoproteins / metabolism
  • Membrane Glycoproteins / pharmacology
  • Phosphatidylserines / metabolism*
  • Protein Binding / physiology
  • Tritium
  • beta 2-Glycoprotein I

Substances

  • Anions
  • Cardiolipins
  • Glycoproteins
  • Lupus Coagulation Inhibitor
  • Membrane Glycoproteins
  • Phosphatidylserines
  • beta 2-Glycoprotein I
  • Tritium
  • Cholesterol