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The Journal of Immunology, 1974, 112: 935-940.
Copyright © 1974 by The American Association of Immunologists, Inc.

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Interaction of the First (C1), the Second (C2) and the Fourth (C4) Component of Complement with Different Preparations of Bacterial Lipopolysaccharides and with Lipid A

Michael Loos, Dieter Bitter-Suermann and Manfred Dierich

Institute of Medical Microbiology, Johannes Gutenberg University, 65 Mainz, Germany

Abstract

Lipopolysaccharides of Gram-negative bacteria (LPS) known to activate the complement system via the alternate pathway bypassing C1, C4, and C2 had a direct effect on purified C1, but no effect on purified C4 and C2. These studies were performed with different preparations of LPS and of Lipid-A isolated from smooth (S-) and rought (R-) forms of Escherichia coli and Salmonella strains. It was shown that the effect of LPS on C1 depends upon the concentration and type of LPS applied: 0.77 µg of LPS from E. coli 0 75, 2.5 µg of LPS from S. minnesota R 595, 24 µg of Lipid-A and 55 µg of Lipid-A/BSA were necessary to get 50% inhibition of free C1. In contrast, 100 µg of LPS from E. coli 0 111, from S minnesota S-form, or from S. minnesota R 345 showed no significant inhibition. Binding of C1 to EA or EAC4 markedly reduced the effect of LPS and of Lipid-A on C1. The inhibition of C1 was shown to be the result of a direct interaction of LPS and of Lipid-A with the C1 subunit C1q: LPS precipitated C1q. LPS and Lipid-A had no effect on the C1 esterase activity against C2.




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M. Drogari-Apiranthitou, E. J. Kuijper, N. Dekker, and J. Dankert
Complement Activation and Formation of the Membrane Attack Complex on Serogroup B Neisseria meningitidis in the Presence or Absence of Serum Bactericidal Activity
Infect. Immun., July 1, 2002; 70(7): 3752 - 3758.
[Abstract] [Full Text] [PDF]




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