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黏附蛋白在人血小板α-颗粒电子透明基质中两个新划分区域的定位。

Localization of adhesive proteins in two newly subdivided zones in electron-lucent matrix of human platelet alpha-granules.

作者信息

Suzuki H, Katagiri Y, Tsukita S, Tanoue K, Yamazaki H

机构信息

Department of Cardiovascular Research, Tokyo Metropolitan Institute of Medical Science, Japan.

出版信息

Histochemistry. 1990;94(4):337-44. doi: 10.1007/BF00266440.

Abstract

Platelet alpha-granules have been reported to consist of two zones, nucleoid and electron-lucent matrix, with different densities under electron microscopy. When washed human platelets were prepared by a rapid freeze-substitution method using liquid helium, we found that the electron-lucent matrix could be further subclassified into two zones having different densities: the intermediate and the light zones. The light zone was located at the periphery opposite the most dense nucleoid and contained several tubular structures with diameters of about 20 nm. The intermediate zone often laid between the nucleoid and light zone. By careful inspection, intermediate and light zones could even be identified in the platelets embedded in Lowicryl K4M, which where then used to localize several adhesive proteins in these two zone by immunocytochemical studies using the respective polyclonal antibodies. Fibrinogen, thrombospondin, and fibronectin were detected only in the intermediate zone. In contrast, von Willebrand factor (vWF) was localized only in the light zone, suggesting an association between vWF and the tubular structures in the light zone. In the nucleoid, none of these adhesive proteins were detected. Glycoprotein IIb/IIIa, a receptor for these adhesive proteins on the platelet surface, was detected not only on the outer surface of the cell membranes but also on the inner surface of the alpha-granule membrane. These data indicate that two zones with different densities in electron-lucent matrix and functions exist in the platelet alpha-granules.

摘要

据报道,在电子显微镜下,血小板α颗粒由两个区域组成,即类核区和电子透明基质区,密度不同。当使用液氦通过快速冷冻置换法制备洗涤后的人血小板时,我们发现电子透明基质可进一步细分为两个密度不同的区域:中间区和亮区。亮区位于与密度最高的类核区相对的外周,包含几个直径约20nm的管状结构。中间区常位于类核区和亮区之间。通过仔细观察,甚至在包埋于Lowicryl K4M中的血小板中也能识别出中间区和亮区,然后使用各自的多克隆抗体通过免疫细胞化学研究将几种黏附蛋白定位在这两个区域。仅在中间区检测到纤维蛋白原、血小板反应蛋白和纤连蛋白。相反,血管性血友病因子(vWF)仅定位在亮区,这表明vWF与亮区的管状结构有关。在类核区,未检测到这些黏附蛋白中的任何一种。血小板表面这些黏附蛋白的受体糖蛋白IIb/IIIa不仅在细胞膜外表面检测到,而且在α颗粒膜内表面也检测到。这些数据表明,血小板α颗粒中电子透明基质存在两个密度和功能不同的区域。

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