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Inflammatory particles stimulate thromboplastin production by human monocytes
Thrombosis Research
|May 15, 1983
Summary
Inflammatory agents like asbestos and zymosan increase thromboplastin activity in human monocytes, a process dependent on protein synthesis. This finding suggests a role for monocytes in fibrin deposition during inflammation.
Area of Science:
- Immunology
- Cell Biology
- Hematology
Background:
- Inflammatory lesions often exhibit fibrin deposition.
- The role of inflammatory stimuli in monocyte procoagulant activity is not fully understood.
Purpose of the Study:
- To investigate the effect of various inflammatory particles and soluble agents on thromboplastin activity in human monocytes.
- To elucidate the mechanisms underlying the observed changes in procoagulant activity.
Main Methods:
- Cultured human monocytes were exposed to different inflammatory agents (zymosan, asbestos, carrageenan, dextran sulfate, latex, anatase).
- Thromboplastin activity was measured.
- The role of protein synthesis and endotoxin contamination was assessed.
Main Results:
- Potent inflammatory particles and dextran sulfate dose- and time-dependently increased monocyte thromboplastin activity.
- Weakly inflammatory particles showed minimal effect.
- The increase in activity was protein synthesis-dependent, slow to peak (around 18 hours), and not attributable to endotoxin.
Conclusions:
- Certain inflammatory stimuli significantly enhance monocyte thromboplastin activity.
- This procoagulant effect, dependent on protein synthesis, may contribute to fibrin deposition in inflammatory sites.
- Monocytes play a crucial role in the coagulation cascade during inflammatory responses.