Uiker S, Kriz W
Institute of Anatomy and Cell Biology I, University of Heidelberg, Germany.
Virchows Arch. 1995;426(3):281-93. doi: 10.1007/BF00191366.
The goal of this study has been to characterize the process of glomerular microaneurysm formation and to separate it from capillary ballooning. In the Habu venom model glomerular capillary ballooning and glomerular microaneurysm formation are seen regularly. The sequence of glomerular lesions leading to a glomerular microaneurysm has been examined and it is clear that the process starts with local mesangiolysis. This may proceed to mesangial expansion and/or ballooning of glomerular capillaries but in contrast to ballooning the formation of a glomerular microaneurysm is based on endothelial defects. The process occurs as follows: once initiated by mesangial failure lesions extend along the mesangial axis. As long as the extension of the lesion encroaches on divergent capillary branches, capillary ballooning by "coalescence" is the result. This process comes to an end when convergent capillary branching is reached and two capillaries join. At this point endothelial disruptions occur, blood and mesangial spaces merge and a glomerular microaneurysm is established. Further growth of the microaneurysm occurs following damage spreading along the lobular axis. The entire process has been reconstructed and is presented in a three-dimensional model.
本研究的目的是描述肾小球微动脉瘤形成的过程,并将其与毛细血管扩张区分开来。在哈布蛇毒模型中,经常可以看到肾小球毛细血管扩张和肾小球微动脉瘤形成。已经对导致肾小球微动脉瘤的肾小球病变序列进行了研究,很明显这个过程始于局部系膜溶解。这可能会发展为系膜扩张和/或肾小球毛细血管扩张,但与扩张不同的是,肾小球微动脉瘤的形成是基于内皮缺陷。这个过程如下:一旦由系膜功能障碍引发,病变就会沿着系膜轴延伸。只要病变的延伸侵犯到分歧的毛细血管分支,通过“融合”导致的毛细血管扩张就是结果。当到达汇聚的毛细血管分支且两条毛细血管汇合时,这个过程就结束了。此时会发生内皮破坏,血液和系膜间隙融合,从而形成肾小球微动脉瘤。微动脉瘤的进一步生长是在损伤沿着小叶轴扩散之后发生的。整个过程已经重建,并以三维模型呈现。