Sulfatides are associated with neointimal thickening after vascular injury
Sulfatides are associated with neointimal thickening after vascular injury
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DOI:
10.1016/j.atherosclerosis.2010.01.033
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发表时间:
2010-07-01
期刊:
影响因子:
5.3
通讯作者:
Node, K.
中科院分区:
文献类型:
--
作者:
Inoue, T.;Taguchi, I.;Node, K.
Background: Sulfatides are known to be a native ligand of P-selectin. Platelet-leukocyte interaction via the cross-talk between P-selectin and Mac-1 (CD11b/CD18) plays an important role in the mechanism of neointimal thickening after vascular injury such as that seen in post-stent restenosis. However, the roles of sulfatides on restenosis have not been elucidated.Methods: Serum sulfatide levels, P-selectin expression on the surface of platelets, and activated Mac-1 on the surface of neutrophils were serially measured using both coronary sinus and peripheral blood samples in 21 patients who underwent coronary stent implantation.Results: The trans-cardiac gradient (coronary sinus minus peripheral blood) of the sulfatide levels significantly increased at 15 min (-1.47 +/- 2.87 to 0.59 +/- 1.44 nmol/ml, p < 0.001), compared to baseline levels. The maximum response of the trans-cardiac gradient of P-selectin expression on the surface of platelets at 15 min after stent implantation (R = 0.55, p < 0.01), and that of activated Mac-1 on the surface of neutrophils at 48 h (R = 0.59, p < 0.01), were both positively correlated with that of serum sulfatide levels at 15 min. The angiographic late lumen loss was correlated with the trans-cardiac gradient of sulfatide levels at 15 min (R = 0.48, p < 0.05), platelet P-selectin expression at 15 min (R = 0.42, p < 0.05) and activated neutrophil Mac-1 expression at 48 h (R = 0.46, p < 0.05), but not with values at other sampling points.Conclusions: Sulfatides may play a physiological role on inflammation in vascular injury and the development of neointimal thickening. (C) 2010 Elsevier Ireland Ltd. All rights reserved.