Editorial |
From the Departments of Cardiology and Cell Biology, Cleveland Clinic Foundation, Cleveland, Ohio.
Correspondence to Marc S. Penn, MD, PhD, Departments of Cardiology and Cell Biology, Cleveland Clinic Foundation, NC10, 9500 Euclid Ave, Cleveland, OH 44915. E-mail pennm@ccf.org
Key Words: thrombosis acute coronary syndrome restenosis
Tissue factor
(TF) is a cell surface protein that is expressed by
endothelial cells, monocytes, and smooth muscle cells
in response to a variety of stimuli including
lipopolysaccharide,1 growth factors,2 and
lipoproteins3 (Figure
).
The main function of TF is to bind coagulation factor VII, leading to
activation of both the intrinsic and extrinsic blood coagulation
cascades.4 In normal
arteries, TF expression is limited to the adventitia except for
sporadic expression in the
media.5 Although TF is
important in maintaining vascular integrity in response to injury,
abnormal TF expression has broad-ranging importance in a variety of
human diseases including disseminated intravascular coagulation in
patients with sepsis6 and
arterial thrombosis in patients with unstable
angina.7
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In this issue of Circulation Research, Singh et al8 further our understanding of the importance of TF in vascular disease by demonstrating the importance of TF expression on the development of neointimal growth in response to hemostasis. Previous studies using this model of carotid artery ligation leading to smooth muscle cell hyperplasia and neointimal formation9 have demonstrated the necessity of fibrin deposition for the smooth muscle cell migration and proliferation to occur.10
This study by Singh et
al8 also furthers our
understanding of the importance of TF in the generation of local fibrin
deposition. They showed that in response to blood hemostasis, TF, but
not
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