Activated platelets stimulate tissue factor expression in smooth muscle cells

Tissue factor (TF)-induced activation of the coagulation plays a key role in the pathophysiology of acute coronary syndromes. Because TF represents the initial trigger of the coagulation cascade, its expression in the arterial wall is tightly regulated. Objective: To determine whether and which solu...

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Veröffentlicht in:Thrombosis research 2003, Vol.112 (1), p.51-57
Hauptverfasser: Cirillo, Plinio, Golino, Paolo, Calabrò, Paolo, Ragni, Massimo, Forte, Lavinia, Piro, Orlando, De Rosa, Salvatore, Pacileo, Mario, Chiariello, Massimo
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Sprache:eng
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Zusammenfassung:Tissue factor (TF)-induced activation of the coagulation plays a key role in the pathophysiology of acute coronary syndromes. Because TF represents the initial trigger of the coagulation cascade, its expression in the arterial wall is tightly regulated. Objective: To determine whether and which soluble mediators released during platelet activation may upregulate TF expression in smooth muscle cells (SMCs). Methods and results: Rabbit SMCs were challenged with collagen-activated platelets and their effects on TF mRNA transcription and protein expression were evaluated at different time points (30 min, 1, 2, 4, 8, 12 and 24 h) by RT-PCR, immunofluorescence and a two-stage colorimetric assay. A progressive increase in TF mRNA, peaking at 2 h, was evident in SMCs stimulated with activated platelets with respect to baseline. The increase in TF mRNA expression was associated with a parallel increase in TF protein, as demonstrated by immunofluorescence and by colorimetric assay. In a different set of experiments, selected platelet-derived soluble mediators were shown to induce TF mRNA expression. Conclusions: Activated platelets upregulate TF, via release of several soluble mediators, in a cell population widely expressed in the vessel wall and in atherosclerotic plaques, such as SMCs. This phenomenon might play an important role in sustaining thrombus formation in vivo.
ISSN:0049-3848
1879-2472
DOI:10.1016/j.thromres.2003.11.011