Tubing loops as a model for cardiopulmonary bypass circuits: Both the biomaterial and the blood-gas phase interfaces induce complement activation in anin vitro model
- 1 July 1996
- journal article
- research article
- Published by Springer Nature in Journal of Clinical Immunology
- Vol. 16 (4) , 222-229
- https://doi.org/10.1007/bf01541228
Abstract
We describe here a model for the study of blood/surface and blood/air interaction as encountered in cardiopulmonary bypass (CPB) circuits. Polyethylene tubing was filled with serum or blood and closed end to end into loops whereby the volume of the remaining air bubble was inversely varied with respect to that of the fluid. The loops were rotated vertically in a water bath at 37°C. The profiles of C3a, iC3, and TCC generation were similar to those observed at surgery, involving CPB. Soluble heparin and heparan sulfate inhibited both C3a and TCC formation, but surface-conjugated heparin had only a minor effect. Binding of C3 and/or C3 fragments to the heparin surface was much reduced compared to the amine matrix to which heparin was linked, but compared with the polyethylene surface the effect was less pronounced. These data suggest that, in addition to the biomaterial surface, the blood-gas interface seems to play an important role in the activation of complement and that this activation is inhibitable by high concentrations of soluble glucose aminoglycans.Keywords
This publication has 32 references indexed in Scilit:
- Complement activation during cardiopulmonary bypass: Effects of immobilized heparinThe Annals of Thoracic Surgery, 1994
- Evidence for iC3 generation during cardiopulmonary bypass as the result of blood-gas interactionClinical and Experimental Immunology, 1993
- Assessing the effect of cardiopulmonary bypass on the brainThe Annals of Thoracic Surgery, 1991
- Biology of complement: the overtureImmunology Today, 1991
- The response of human platelets to activated components of the complement systemImmunology Today, 1991
- Inhibition of complement dependent experimental inflammation in human skin by different heparin fractionsInternational Journal of Immunopharmacology, 1986
- An Assessment of the Extent of Antigenic Analogy between Physiologically Bound C3 and C3 Denatured by Sodium Dodecyl SulphateScandinavian Journal of Immunology, 1985
- Heparin prevents formation of the human C3 amplification convertase by inhibiting the binding site for B on C3bMolecular Immunology, 1983
- Formation of the initial C3 convertase of the alternative complement pathway. Acquisition of C3b-like activities by spontaneous hydrolysis of the putative thioester in native C3.The Journal of Experimental Medicine, 1981
- Structural Determinants of the Capacity of Heparin to Inhibit the Formation of the Human Amplification C3 ConvertaseJournal of Clinical Investigation, 1981