Wagner R C, Robinson C S
Microvasc Res. 1984 Sep;28(2):197-205. doi: 10.1016/0026-2862(84)90017-7.
Conventional electron microscopy of thin sections through capillary walls is inadequate to discern the relationships between endothelial vesicles and their association with the cell surface. High-voltage electron microscopy of thick sections through diaphragm muscle capillaries has been employed to visualize the three-dimensional structure of the vesicular system. Stereopairs of thick sections provide for direct three-dimensional observations of samples several vesicle diameters deep. A variety of simple and compound vesicular forms are present but not all are conjoined or maintain connections with the endothelial cell surface. This contributes to the concept of a dynamic interaction between free and attached vesicular structures where fission and fusion events compartmentalize and reconnect repeatedly. Such interactions would provide for a discontinuous pathway across the capillary wall but with a higher degree of complexity than a simple shuttling mechanism.
通过毛细血管壁薄切片的传统电子显微镜检查不足以辨别内皮小泡之间的关系及其与细胞表面的关联。已采用通过膈肌毛细血管厚切片的高压电子显微镜来观察小泡系统的三维结构。厚切片的立体对可对深度达几个小泡直径的样本进行直接三维观察。存在多种简单和复合的小泡形式,但并非所有小泡都与内皮细胞表面相连或保持连接。这有助于形成游离和附着的小泡结构之间动态相互作用的概念,其中裂变和融合事件反复地进行分隔和重新连接。这种相互作用将提供一条穿过毛细血管壁的不连续途径,但比简单的穿梭机制具有更高的复杂性。