beta(2)-glycoprotein I (Apolipoprotein H) modulates uptake and endocytosis associated chemiluminescence in rat Kupffer cells

beta(2)-glycoprotein I (Apolipoprotein H) modulates uptake and endocytosis associated chemiluminescence in rat Kupffer cells

Author Gomes, L. F. Google Scholar
Goncalves, L. M. Google Scholar
Fonseca, FLA Google Scholar
Celli, C. M. Google Scholar
Videla, L. A. Google Scholar
Chaimovich, H. Google Scholar
Junqueira, VBC Google Scholar
Institution Universidade de São Paulo (USP)
Univ Chile
Universidade Federal de São Paulo (UNIFESP)
Baylor Coll Med
Abstract beta(2)-Glycoprotein I (beta(2)GPI) is known to influence macrophage uptake of particles with phosphatidylserine containing surfaces, as apoptotic thymocytes and unilamellar vesicles in vitro. Nevertheless, effects upon macrophage activation induced by this interaction are still unknown. beta(2)GPI influence upon the reactive species production by Kupffer cells was evaluted in order to investigate whether beta(2)GPI modulates the macrophage response to negatively charged surfaces. Chemiluminescence of isolated nonparenchymal rat liver cells was measured after phagocytosis of opsonized zymosan or phorbolmyristate acetate (PMA) stimulation, in the presence and absence of large unilamellar vesicles (LUVs) containing 25 mol% phosphatidylserine (PS) or 50 mol% cardiolipin (CL) and complementary molar ratio of phosphatidylcholine (PC). beta(2)GPI decreased by 50% the chemiluminescence response induced by opsonized zymosan, with a 66% reduction of the initial light emission rate. PMA stimulated Kupffer cell chemiluminescence was insensitive to human or rat beta(2)GPI. Albumin (500 mug/ml) showed no effect upon chemiluminescence. beta(2)GPI increased PS/PC LUV uptake and degradation by Kupffer cells in a concentration-dependent manner, without leakage of the internal contents of the LUVs, as shown by fluorescence intensity enhancement. LUVs opsonized with antiphospholipid antibodies (aPL) from syphilitic patients increased light emission by Kupffer cells. Addition of beta(2)GPI to the assay reduced chemiluminescence due to opsonization with purified IgG antibodies from systemic lupus erythematosus (SLE or syphilis (Sy) patient sera. A marked net increase in chemiluminescence is observed in the presence of Sy aPL antibodies, whereas a decrease was found when SLE aPL were added to the assay, in the presence or absence of beta(2)GPI. At a concentration of 125 mug/ml, beta(2)GPI significantly reduced Kupffer cell Candida albicans phagocytosis index and killing score by 50 and 10%, respectively the present data strongly suggest that particle uptake in the presence of beta(2)GPI is coupled to an inhibition of reactive species production by liver macrophages during the respiratory burst, supporting the role of beta(2)GPI as a mediator of senescent cell removal.
Keywords apolipoprotein H (beta(2)-glycoprotein I)
Kupffer cell
macrophage activation
phospholipid vesicles
Language English
Date 2002-07-01
Published in Free Radical Research. Abingdon: Taylor & Francis Ltd, v. 36, n. 7, p. 741-747, 2002.
ISSN 1071-5762 (Sherpa/Romeo, impact factor)
Publisher Taylor & Francis Ltd
Extent 741-747
Access rights Closed access
Type Article
Web of Science ID WOS:000176434600004

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