2006
DOI: 10.1055/s-2006-933336
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Sources of Tissue Factor

Abstract: Tissue factor (TF) exhibits a distinct nonuniform tissue distribution. Thus, high levels are found in highly vascularized organs such as the lung, brain, and placenta; intermediate levels in the heart, kidney, intestine, testes, and uterus; and low levels in the spleen, thymus, and liver. Several cell types are known to express TF constitutively, such as astrocytes in the brain, epithelial cells enveloping organs and body surfaces, adventitial fibroblasts and pericytes, and cardial myocytes in the heart. Smoot… Show more

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Cited by 224 publications
(194 citation statements)
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References 97 publications
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“…Unique among cells, monocytes not only secrete a repertoire of pro-and anti-inflammatory cytokines, but are the only blood cells known to synthesize the procoagulant molecule TF (44,45). In this study, we explored the possibility that recombinant activated protein C dampens the proinflammatory and procoagulant potential of activated monocytes by up-regulating the production of the anti-inflammatory cytokine IL-10 and by inhibiting TF activity.…”
Section: Discussionmentioning
confidence: 99%
“…Unique among cells, monocytes not only secrete a repertoire of pro-and anti-inflammatory cytokines, but are the only blood cells known to synthesize the procoagulant molecule TF (44,45). In this study, we explored the possibility that recombinant activated protein C dampens the proinflammatory and procoagulant potential of activated monocytes by up-regulating the production of the anti-inflammatory cytokine IL-10 and by inhibiting TF activity.…”
Section: Discussionmentioning
confidence: 99%
“…7,[11][12][13] A variety of inflammatory stimuli, including bacterial cell products and components of the complement system, are known to promote the expression of tissue factor (TF) on the surface of endothelial cells, monocytes, and neutrophils. [14][15][16] In view of previous studies showing that aberrant TF expression may be responsible for thrombosis, we considered the possibility that increased TF expression induces pathological activation of the coagulation pathway, placental failure, fetal death, and growth restriction in this model of spontaneous abortion.…”
Section: Introductionmentioning
confidence: 99%
“…TF is the clotting initiator [24][25][26] and a structural member of the cytokine receptor family, which signifies the expansion of the adaptive immune system in vertebrates, indicating a close connection of the coagulation pathways with the host response to infection 27 . Accordingly, TF has been increasingly recognized as the interface between coagulation and inflammation [27][28][29][30][31][32] .…”
mentioning
confidence: 99%