Bacterial killing and inhibition of inner membrane activity by C5b-9 complexes as a function of the sequential addition of C9 to C5b-8 sites.
Open Access
- 15 November 1990
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Immunology
- Vol. 145 (10) , 3367-3371
- https://doi.org/10.4049/jimmunol.145.10.3367
Abstract
The assembly of the C5b-9 complex on the outer membrane of C-sensitive cells of Escherichia coli results in a rapid inhibition of inner membrane function and ultimately a loss of cell viability. Cells bearing C5b-8 sites suffer no deleterious effects; however, the addition of C9 results in a rapid inhibition of inner membrane function and cell death. An attempt was made to examine the relationship between the toxic effects of the C5b-9 complex and the number of C9 molecules per C5b-8 site. Cells bearing C5b-8 sites were exposed to excess C9 at 0 degrees C and washed three times at 4 degrees C. The number of C9 molecules bound to each cell was equivalent to the number of C5b-8 sites present on each cell, and no additional C9 molecules could be bound when the cells were maintained at 4 degrees C. These cells were then incubated at 37 degrees C for 3 min and returned to 0 degrees C, a technique which exposed additional C9-binding sites equivalent to the number of C9 molecules previously bound to the cells. This technique was repeated and demonstrated that the sequential build-up of a C5b-9 site with two C9 molecules per C5b-8 site was capable of inhibiting both inner membrane function (respiration and amino acid transport) and cell viability. Three C9 molecules per complex had effects that approached the inhibitory effects of complexes formed in the presence of excess C9.This publication has 25 references indexed in Scilit:
- Activation of complement by serum-resistant Neisseria gonorrhoeae. Assembly of the membrane attack complex without subsequent cell death.The Journal of Experimental Medicine, 1982
- Studies on the mechanism of bacterial resistance to complement-mediated killing. II. C8 and C9 release C5b67 from the surface of salmonella minnesota S218 because the terminal complex does not insert into the bacterial outer membraneThe Journal of Experimental Medicine, 1982
- Studies on the mechanism of bacterial resistance to complement-mediated killing. I. Terminal complement components are deposited and released from salmonella minnesota S218 without causing bacterial deathThe Journal of Experimental Medicine, 1982
- Polymerization of the ninth component of complement (C9): formation of poly(C9) with a tubular ultrastructure resembling the membrane attack complex of complement.Proceedings of the National Academy of Sciences, 1982
- The eighth component of human complement. Purification and physicochemical characterization of its unusual subunit structure.Journal of Biological Chemistry, 1980
- Mathematical analysis of the reaction of EAC1-8 with C9: identification of parameters defining conditions for molecular titration.The Journal of Immunology, 1980
- Sequential metabolic expressions of the lethal process in human serum-treated Escherichia coli: role of lysozymeInfection and Immunity, 1980
- Molecular nature of the complement lesion.Proceedings of the National Academy of Sciences, 1978
- STUDIES ON TERMINAL STAGES OF IMMUNE HEMOLYSIS .3. DISTINCTION BETWEEN INSERTION OF C9 AND FORMATION OF A TRANSMEMBRANE CHANNEL1978
- Immune Lytic Transformation: A State of Irreversible Damage Generated as a Result of the Reaction of the Eighth Component in the Guinea Pig Complement SystemThe Journal of Immunology, 1968