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动脉壁的介入性热损伤:血管性血友病因子的展开及其在55摄氏度加热后与胶原蛋白结合增加。

Interventional thermal injury of the arterial wall: unfolding of von Willebrand factor and its increased binding to collagen after 55 degrees C heating.

作者信息

Post M J, de Graaf-Bos A N, Posthuma G, de Groot P G, Sixma J J, Borst C

机构信息

Department of Cardiology, Utrecht University Hospital, The Netherlands.

出版信息

Thromb Haemost. 1996 Mar;75(3):515-9.

PMID:8701418
Abstract

PURPOSE

Thermal angioplasty alters the thrombogenicity of the arterial wall. In previous studies, platelet adhesion was found to increase after heating human subendothelium to 55 degrees C and decrease after heating to 90 degrees C. In the present electron microscopic study, the mechanism of this temperature-dependent platelet adhesion to the heated arterial wall is elucidated by investigating temperature-dependent conformational changes of von Willebrand factor (vWF) and collagen types I and III and the binding of vWF to heated collagen.

METHODS

Purified vWF and/or collagen was applied to electron microscopic grids and heated by floating on a salt-solution of 37 degrees C, 55 degrees C or 90 degrees C for 15 s. After incubation with a polyclonal antibody against vWF and incubation with protein A/gold, the grids were examined by electron microscopy.

RESULTS

At 37 degrees C, vWF was coiled. At 55 degrees C, vWF unfolded, whereas heating at 90 degrees C caused a reduction in antigenicity. Collagen fibers heated to 37 degrees C were 60.3 +/- 3.1 nm wide. Heating to 55 degrees C resulted in the unwinding of the fibers, increasing the width to 87.5 +/- 8.2 nm (p < 0.01). Heating to 90 degrees C resulted in denatured fibers with an enlarged width of 85.1 +/- 6.1 nm (p < 0.05). Heating of collagen to 55 degrees C resulted in an increased vWF binding as compared to collagen heated to 37 degrees C or to 90 degrees C. Incubation of collagen with vWF, prior to heating, resulted in a vWF binding after heating to 55 degrees C that was similar to the 37 degrees C binding and a decreased binding after 90 degrees C.

CONCLUSIONS

After 55 degrees C heating, the von Willebrand factor molecule unfolds and collagen types I and III exhibit an increased adhesiveness for von Willebrand factor. Heating to 90 degrees C denatures von Willebrand factor and collagen. The conformation changes of von Willebrand factor and its altered binding to collagen type I and III may explain the increased and decreased platelet adhesion to subendothelium after 55 degrees C and 90 degrees C heating, respectively.

摘要

目的

热血管成形术会改变动脉壁的血栓形成倾向。在先前的研究中,发现将人内皮下层加热至55℃后血小板黏附增加,而加热至90℃后血小板黏附减少。在本电子显微镜研究中,通过研究血管性血友病因子(vWF)以及I型和III型胶原的温度依赖性构象变化以及vWF与加热后胶原的结合,阐明了这种温度依赖性血小板与加热后动脉壁黏附的机制。

方法

将纯化的vWF和/或胶原应用于电子显微镜载网,并通过漂浮在37℃、55℃或90℃的盐溶液上加热15秒。在用抗vWF多克隆抗体孵育并与蛋白A/金孵育后,通过电子显微镜检查载网。

结果

在37℃时,vWF呈卷曲状。在55℃时,vWF展开,而在90℃加热导致抗原性降低。加热至37℃的胶原纤维宽度为60.3±3.1nm。加热至55℃导致纤维解旋,宽度增加至87.5±8.2nm(p<0.01)。加热至90℃导致纤维变性,宽度增大至85.1±6.1nm(p<0.05)。与加热至37℃或90℃的胶原相比,将胶原加热至55℃导致vWF结合增加。在加热前将胶原与vWF孵育,加热至55℃后vWF结合与37℃时相似,而在90℃后结合减少。

结论

在55℃加热后,血管性血友病因子分子展开,I型和III型胶原对血管性血友病因子的黏附性增加。加热至90℃使血管性血友病因子和胶原变性。血管性血友病因子的构象变化及其与I型和III型胶原结合的改变可能分别解释了在55℃和90℃加热后血小板与内皮下层黏附的增加和减少。

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