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Thrombin‐induced chemotaxis and aggregation of neutrophils
Author(s) -
Bizios Rena,
Lai Linda,
Fenton John W.,
Malik Asrar B.
Publication year - 1986
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041280318
Subject(s) - chemotaxis , thrombin , chemistry , thrombin generation , microbiology and biotechnology , biophysics , biochemistry , immunology , biology , receptor , platelet
Thrombin‐induced neutrophil chemotaxis and aggregation were studied using cells isolated from either human or sheep blood. Sheep neutrophils (10 8 cells/ml) exhibited maximum chemotactic migration towards 10 −8 M human α ‐thrombin, 10 −8 M γ‐thrombin (which lacks the fibrinogen site), and 10 −12 M D ‐Phe‐Pro‐Arg‐CH 2 ‐α‐thrombin (catalytically inactive thrombin). Chemotactic responses of the same magnitude were obtained with human neutrophils (10 8 cells/ml). The chemotactic responses to thrombin were comparable to those obtained with diluted (1:200 v/v) zymosan activated serum (ZAS) and 10 −11 M FMLP. Premixing of the thrombin forms with hirudin in 1:1 stoichiometric amounts abolished the chemotaxis but not chemokinesis Aggregatory responses of human and sheep neutrophils were comparable for ZAS, α‐thrombin, and γ‐thrombin. The responses of both human and sheep neutrophils to D ‐Phe‐Pro‐Arg‐CH 2 ‐α‐thrombin were attenuated, indicating that the proteolytic site may be involved in the aggregatory response. The results suggest that thrombin‐induced neutrophil chemotaxis and aggregation are mediated by different mechanisms, since chemotaxis is a catalytically independent response whereas aggregation is an active site independent response.