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Marsche, G; Furtmüller, PG; Obinger, C; Sattler, W; Malle, E.
Hypochlorite-modified high-density lipoprotein acts as a sink for myeloperoxidase in vitro.
Cardiovasc Res. 2008; 79(1): 187-194. Doi: 10.1093/cvr/cvn051 [OPEN ACCESS]
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Führende Autor*innen der Med Uni Graz
Malle Ernst
Marsche Gunther
Co-Autor*innen der Med Uni Graz
Sattler Wolfgang
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Abstract:
AIMS: Myeloperoxidase (MPO), a cardiovascular risk factor in humans, is an in vivo catalyst for lipoprotein modification via intermediate formation of reactive chlorinating species. Among the different lipoprotein classes, anti-atherogenic high-density lipoprotein (HDL) represents a major target for modification by hypochlorous acid (HOCl), generated from H2O2 by MPO in the presence of physiological chloride concentrations. As MPO was identified as an HDL-associated protein that could facilitate selective oxidative modification of its physiological carrier, the aim of the present study was to investigate whether and to what extent modification of HDL by HOCl affects the binding affinity of MPO in vitro. METHODS AND RESULTS: We show that binding affinity of 125I-labelled MPO to HDL markedly increases as a function of increasing extent of HOCl modification of HDL. In contrast to native HDL, HOCl-HDL potently inhibits MPO binding/uptake by endothelial cells and effectively attenuates metabolism of MPO by macrophages. Reduction of HDL-associated chloramines with methionine strongly impaired binding affinity of MPO towards HOCl-HDL. This indicates that N-chloramines generated by HOCl are regulators of the high-affinity interaction between HOCl-HDL and positively charged MPO. Most importantly, the presence of HOCl-HDL is almost without effect on the halogenating activity of MPO. CONCLUSION: We propose that MPO-dependent modification of HDL and concomitant increase in the binding affinity for MPO could generate a vicious cycle of MPO transport to and MPO-dependent modification at sites of chronic inflammation.
Find related publications in this database (using NLM MeSH Indexing)
Cells, Cultured -
Chloramines - metabolism
Endothelium, Vascular - cytology
Humans -
Hydrogen Peroxide - metabolism
Hypochlorous Acid - metabolism
Lipoproteins, HDL - metabolism
Peroxidase - metabolism
Umbilical Veins - cytology

Find related publications in this database (Keywords)
hypochlorous acid
ApoA-I
inflammation
neutrophils
MPO-hydrogen peroxide-halide system
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