Antiga L, Ene-Iordache B, Remuzzi G, Remuzzi A
Clinical Research Center for Rare Diseases Aldo e Cele Daccò, Mario Negri Institute for Pharmacological Research, Villa Camozzi, Ranica, BG, Italy.
Microvasc Res. 2001 Nov;62(3):346-54. doi: 10.1006/mvre.2001.2351.
Glomerular structural changes are conventionally investigated by optical or electron microscopy on two-dimensional (2D) sections. To understand the relationship between functional and structural changes of glomerular capillary networks in more detail, three-dimensional (3D) investigation of the capillary tufts is required. Since confocal microscopy and scanning electron microscopy cannot completely show the 3D topological organization of the capillary tuft, we have developed an automatic method to obtain a 3D model of the glomerular capillary lumen structure and to derive its topological organization. Serial semithin sections of a glomerular tuft, from rat kidney tissue, were digitized at high resolution. Capillary lumens were digitally outlined and segmented images were automatically aligned. A 3D model of the capillary tuft was automatically generated using the Visualization Toolkit library and the Marching Cubes algorithm. We then developed an original algorithm for automatic 3D skeletonization of capillary lumen volume to identify capillary segments and bifurcations and to obtain the topological organization of the network and geometric parameters of capillary segments (length, radius, and spatial configuration). Capillary segment connectivity was graphically presented in a 2D layout with an automatic procedure, revealing the lobular organization of the network. This technique, successfully applied to serial sections of a glomerular capillary, can be used to study a population of glomerular capillaries to disclose the structural effects of pathological conditions. The methodology can be extended to other vascular structures, such as the microcirculation of neoplastic tissues.
肾小球结构变化传统上是通过光学或电子显微镜对二维(2D)切片进行研究的。为了更详细地了解肾小球毛细血管网络功能和结构变化之间的关系,需要对毛细血管丛进行三维(3D)研究。由于共聚焦显微镜和扫描电子显微镜无法完全显示毛细血管丛的3D拓扑结构,我们开发了一种自动方法来获取肾小球毛细血管腔结构的3D模型并推导其拓扑结构。对大鼠肾脏组织的肾小球丛连续半薄切片进行高分辨率数字化处理。对毛细血管腔进行数字勾勒,并自动对齐分割图像。使用可视化工具包库和移动立方体算法自动生成毛细血管丛的3D模型。然后,我们开发了一种原始算法,用于对毛细血管腔体积进行自动3D骨架化,以识别毛细血管段和分支,并获得网络的拓扑结构和毛细血管段的几何参数(长度、半径和空间构型)。毛细血管段的连通性通过自动程序以二维布局图形化呈现,揭示了网络的小叶结构。这项技术已成功应用于肾小球毛细血管的连续切片,可用于研究一群肾小球毛细血管,以揭示病理状况的结构影响。该方法可扩展到其他血管结构,如肿瘤组织的微循环。