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血小板内部再探:电子断层成像揭示管状α-颗粒亚型。

The platelet interior revisited: electron tomography reveals tubular alpha-granule subtypes.

机构信息

Cell Microscopy Center and Department of Cell Biology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Blood. 2010 Aug 19;116(7):1147-56. doi: 10.1182/blood-2010-02-268680. Epub 2010 May 3.

Abstract

We have used (cryo) electron tomography to provide a 3-dimensional (3D) map of the intracellular membrane organization of human platelets at high spatial resolution. Our study shows that the open canalicular system and dense tubular system are highly intertwined and form close associations in specialized membrane regions. 3D reconstructions of individual alpha-granules revealed large heterogeneity in their membrane organization. On the basis of their divergent morphology, we categorized alpha-granules into the following subtypes: spherical granules with electron-dense and electron-lucent zone containing 12-nm von Willebrand factor tubules, subtypes containing a multitude of luminal vesicles, 50-nm-wide tubular organelles, and a population with 18.4-nm crystalline cross-striations. Low-dose (cryo) electron tomography and 3D reconstruction of whole vitrified platelets confirmed the existence of long tubular granules with a remarkably curved architecture. Immunoelectron microscopy confirmed that these extended structures represent alpha-granule subtypes. Tubular alpha-granules represent approximately 16% of the total alpha-granule population and are detected in approximately half of the platelet population. They express membrane-bound proteins GLUT3 and alphaIIb-beta3 integrin and contain abundant fibrinogen and albumin but low levels of beta-thromboglobulin and no von Willebrand factor. Our 3D study demonstrates that, besides the existence of morphologically different alpha-granule subtypes, high spatial segregation of cargo exists within individual alpha-granules.

摘要

我们使用(冷冻)电子断层扫描技术,以高空间分辨率提供了人类血小板细胞内膜组织的三维(3D)图谱。我们的研究表明,开放小管系统和致密管系统高度交织,并在特化的膜区域形成紧密的关联。对单个α颗粒的 3D 重建显示其膜组织存在很大的异质性。基于其不同的形态,我们将α颗粒分为以下亚型:含 12nm von Willebrand 因子管的电子致密和电子透明区的球形颗粒、含有大量腔囊泡、50nm 宽管状器官和具有 18.4nm 结晶交叉条纹的颗粒。对整个冷冻血小板进行低剂量(冷冻)电子断层扫描和 3D 重建证实了长管状颗粒的存在,其具有显著弯曲的结构。免疫电子显微镜证实这些延伸结构代表α颗粒的亚型。管状α颗粒占总α颗粒群体的约 16%,并且在约一半的血小板群体中检测到。它们表达膜结合蛋白 GLUT3 和 αIIb-β3 整合素,并且含有丰富的纤维蛋白原和白蛋白,但β-血栓球蛋白水平较低,没有 von Willebrand 因子。我们的 3D 研究表明,除了存在形态上不同的α颗粒亚型外,单个α颗粒内还存在货物的高空间隔离。

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