Cardiolipin is a normal component of human plasma lipoproteins

  1. Hiroshi Deguchi*,
  2. José A. Fernández*,
  3. Tilman M. Hackeng*,
  4. Carole L. Banka, and
  5. John H. Griffin*,
  1. Departments of *Molecular and Experimental Medicine and Immunology, The Scripps Research Institute, La Jolla, CA 92037
  1. Communicated by Ernest Beutler, The Scripps Research Institute, La Jolla, CA (received for review October 14, 1999)

Abstract

Anticardiolipin (anti-CL) antibodies, diagnostic for antiphospholipid antibody syndrome, are associated with increased risks of venous and arterial thrombosis. Because CL selectively enhances activated protein C/protein S-dependent anticoagulant activities in purified systems and because CL is not known to be a normal plasma component, we searched for CL in plasma. Plasma lipid extracts [chloroform/methanol (2:1, vol/vol)] were subjected to analyses by using TLC, analytical HPLC, and MS. A plasma lipid component was purified that was indistinguishable from reference CL (M:1448). When CL in 40 fasting plasma lipid extracts (20 males, 20 females) was quantitated by using HPLC, CL (mean ± SD) was 14.9 ± 3.7 μg/ml (range 9.1 to 24.2) and CL was not correlated with phosphatidylserine (3.8 ± 1.7 μg/ml), phosphatidylethanolamine (64 ± 20 μg/ml), or choline-containing phospholipid (1,580 ± 280 μg/ml). Based on studies of fasting blood donors, CL (≥94%) was recovered in very low density, low density, and high density lipoproteins (11 ± 5.3%, 67 ± 11.0%, and 17 ± 10%, respectively), showing that the majority of plasma CL (67%) is in low density lipoprotein. Analysis of relative phospholipid contents of lipoproteins indicated that high density lipoprotein is selectively enriched in CL and phosphatidylethanolamine. These results shows that CL is a normal plasma component and suggest that the epitopes of antiphospholipid antibodies could include CL or oxidized CL in lipoproteins or in complexes with plasma proteins (e.g., β2-glycoprotein I, prothrombin, protein C, or protein S) or with platelet or endothelial surface proteins.

Footnotes

  • To whom reprint requests should be addressed at: Department of Molecular and Experimental Medicine, The Scripps Research Institute, MEM180, 10550 North Torrey Pines Road, La Jolla, CA 92037. E-mail: jgriffin{at}scripps.edu.

  • Abbreviations:
    CL,
    cardiolipin;
    PL,
    phospholipid;
    c-PL,
    choline-containing PL;
    ELSD,
    evaporative light scattering detector;
    PC,
    phosphatidylcholine;
    PS,
    phosphatidylserine;
    PE,
    phosphatidylethanolamine;
    SM,
    sphingomyelin;
    VLDL,
    very low density lipoprotein;
    LDL,
    low density lipoprotein;
    HDL,
    high density lipoprotein;
    ox-,
    oxidized;
    APC,
    activated protein C;
    Lp(a),
    lipoprotein(a)
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