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Activation of Neutrophil Granulocytes in an In Vitro Model of a Cardiopulmonary Bypass
Author(s) -
Åsberg Ann Elisabeth,
Videm Vibeke
Publication year - 2005
Publication title -
artificial organs
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.684
H-Index - 76
eISSN - 1525-1594
pISSN - 0160-564X
DOI - 10.1111/j.1525-1594.2005.00162.x
Subject(s) - degranulation , complement system , platelet , chemistry , biomaterial , platelet activation , integrin alpha m , cardiopulmonary bypass , immunology , microbiology and biotechnology , granulocyte , adhesion , in vitro , medicine , biochemistry , biology , receptor , antibody , organic chemistry
Activated neutrophils play a central role in the pathogenesis of postoperative organ dysfunction after surgery with cardiopulmonary bypass. The researchers used an in vitro roller pump model to investigate the relative importance of the biomaterial, platelets, plasma proteins including activated complement, and flow mode on neutrophil activation as shown by the adhesion, degranulation, and increased the surface expression of CD11b. Neutrophil adhesion to the biomaterial increased with platelet addition, but not with plasma. Biomaterial contact activated neutrophils in a serum‐free buffer, but was significantly increased by activated complement. Platelets increased neutrophil degranulation in a serum‐free buffer but tended to reduce it in plasma. CD11b expression increased in both media. Complement activation was higher with neutrophils alone than with neutrophils and platelets combined. The roller pump reduced neutrophil adhesion and increased degranulation compared to passive rotation. Neutrophil interaction with platelets and complement were more important for activation than biomaterial contact and use of the roller pump. Improvement of biocompatibility is dependent on modifying complement activation and platelet interaction with neutrophils.