1985
DOI: 10.1016/0049-3848(85)90035-0
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Effect of a fibrin(ogen)-derived vasoactive peptide on polymorphonuclear leukocyte emigration

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1986
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Cited by 14 publications
(6 citation statements)
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“…Thus, it is expected that inflammatory cells would be recruited to sites of clot formation by chemotactic agents produced by the clot itself. Indeed, fibrin‐derived peptides have been shown to act as chemotactic agents in vitro 30–32 and in vivo ,31 and neutrophils have been shown to have specific receptors for clot constituents 33, 34. Fibrin peptides have also been shown to stimulate other leukocyte functions, such as degranulation 15.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, it is expected that inflammatory cells would be recruited to sites of clot formation by chemotactic agents produced by the clot itself. Indeed, fibrin‐derived peptides have been shown to act as chemotactic agents in vitro 30–32 and in vivo ,31 and neutrophils have been shown to have specific receptors for clot constituents 33, 34. Fibrin peptides have also been shown to stimulate other leukocyte functions, such as degranulation 15.…”
Section: Discussionmentioning
confidence: 99%
“…However, the apparent proinflammatory effects of fibrin(ogen) may involve indirect interactions. For example, some fibrin degradation products (81)(82)(83)(84)(85) and fibrinopeptide B (86) are strongly chemotactic for PMN, monocytes and fibroblasts. In addition, lower molecular weight degradation products of fibrin(ogen) are known to promote granulocyte infiltration and vascular permeability (82,87).…”
Section: Discussionmentioning
confidence: 99%
“…FDPs reportedly stimulate vascular permeability, 82 endothelial cell retraction, 83,84 monocyte/macrophage IL-1 and IL-6 production, 85,86 and leukocyte chemotaxis. [87][88][89] FDPs can be generated via plasmin-mediated proteolysis of fibrin, and mice with reduced or no plasmin have been generated by gene-targeted deletion of plasminogen activators or plasminogen, respectively. 90,91 Such plasmin-deficient mice display increased pathology in glomerulonephritis 92 and arthritis 51,93 models, suggesting that plasmingenerated FDPs may well function in inflammation.…”
Section: Discussionmentioning
confidence: 99%