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Monocyte integrin expression and monocyte-platelet complex formation in humans with coronary restenosis.

机译:患有冠状动脉再狭窄的人的单核细胞整合素表达和单核细胞-血小板复合物的形成。

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摘要

1. In the present study, we sought to determine whether patients with restenosis after coronary stenting possess increased monocyte reactivity, as manifested by a higher level of adhesion molecule expression and an enhanced propensity to form monocyte-platelet aggregates after activation in vitro. 2. Anti-coagulated peripheral venous blood from 24 patients, 10 with and 14 without angiographically verified restenosis, was obtained. Leucocyte antigen expression and the number of leucocyte-platelet complexes were measured by flow cytometry after activation in whole blood. 3. Surface integrin Mac-1 (CD11b/CD18) and VLA-4 (CD49d/ CD29) expression on monocytes and the relative number of monocyte-platelet complexes after in vitro activation were significantly elevated in patients with restenosis compared with patients without restenosis (fluorescence intensities of 1425 +/- 76 vs 1195 +/- 71, 87 +/- 7 vs 65 +/- 6 and 47 +/- 4 vs 29 +/- 3% for for Mac-1, VLA-4 and monocyte-platelet complexes, respectively; P < 0.05 for each parameter). 4. The results suggest that restenosis is associated with increased monocyte VLA-4 and Mac-1 integrin expression and monocyte-platelet complex formation, which can be revealed after activation in vitro.
机译:1.在本研究中,我们试图确定冠状动脉支架置入术后再狭窄患者是否具有增加的单核细胞反应性,这表现为更高水平的粘附分子表达和体外活化后形成单核细胞-血小板聚集体的倾向增加。 2.获得了24例患者的抗凝外周静脉血,其中10例有血管造影证实的再狭窄,14例没有血管造影证实的再狭窄。在全血中活化后,通过流式细胞术测量白细胞抗原表达和白细胞-血小板复合物的数量。 3.与没有再狭窄的患者相比,再狭窄的患者单核细胞表面整合素Mac-1(CD11b / CD18)和VLA-4(CD49d / CD29)的表达以及体外激活后单核细胞-血小板复合物的相对数量显着升高(对于Mac-1,VLA-4和单核细胞,荧光强度分别为1425 +/- 76与1195 +/- 71、87 +/- 7与65 +/- 6和47 +/- 4与29 +/- 3% -血小板复合物;每个参数P <0.05)。 4.结果表明再狭窄与单核细胞VLA-4和Mac-1整联蛋白表达增加以及单核细胞-血小板复合物形成有关,这可以在体外激活后发现。

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