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首页> 外文期刊>Nephron >Recovery of damaged glomerular capillary network with endothelial cell apoptosis in experimental proliferative glomerulonephritis.
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Recovery of damaged glomerular capillary network with endothelial cell apoptosis in experimental proliferative glomerulonephritis.

机译:实验性增生性肾小球肾炎中受损的肾小球毛细血管网络与内皮细胞凋亡的恢复。

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Capillary repair can occur in damaged glomeruli in recovery models of glomerulonephritis (GN). In order to clarify whether capillary repair is an essential component in glomerular recovery from GN, we have examined the development of the capillary repair after inflammatory injury in both the repairing glomeruli and the segmental sclerotic scar lesions in Thy-1 GN. Mesangiolytic glomerular damage was induced in rats with anti-Thy-1.1 antibody administration. Diffuse mesangiolysis and segmental microaneurysmal ballooning developed in damaged glomeruli by day 3, with reduction of endothelial cellularity. Thereafter, histological proliferative GN developed between day 5 and week 3. Endothelial cell proliferation began on day 1 and peaked on day 5, and the number of glomerular endothelial cells increased and exceeded the level of control values on day 7. Angiogenic glomerular capillary repair occurred through the process of not only capillary regeneration from remaining endothelial cells in capillary aneurysmal lesions but also new capillary growth derived from the glomerular vascular poles by day 7. The number of glomerular capillary lumina also increased to the level of controls by week 3. Subsequently, mesangial proliferative GN resolved, and most of the glomeruli recovered to their normal structure with the reconstruction of the capillary network by weeks 4-6. In the glomerular capillary repair, significant apoptosis of glomerular endothelial cells was present during the period of mild endothelial cell hypercellularity between day 7 and day 10 (0.06 +/- 0.02 apoptotic endothelial cells/glomerular cross section vs. 0.00 +/- 0.00 in controls, mean +/- SEM; p < 0.05. In Thy-1 GN, most of the damaged glomeruli recovered with angiogenic capillary repair. However, segmental sclerotic scar lesions remained in 10-30% of the glomeruli with an incomplete repair of glomerular capillaries. Therefore, it is concluded that following the destruction of the glomerular capillary network in GN, angiogenic capillary repair plays an essential role in the recovery of damaged glomeruli, and incomplete capillary repair leads to sclerotic scar lesions in damaged glomeruli. Glomerular capillary repair occurs through the process of capillary regeneration from remaining endothelial cells as well as new glomerular capillary growth from the glomerular vascular poles. In glomerular capillary repair, apoptosis is necessary in regulating the number of intrinsic endothelial cells.
机译:在肾小球肾炎(GN)恢复模型中,受损的肾小球中可能发生毛细管修复。为了阐明毛细血管修复是否是从GN肾小球恢复中必不可少的组成部分,我们检查了Thy-1 GN的肾小球修复和节段性硬化性瘢痕病变中炎症损伤后毛细血管修复的发展。服用抗Thy-1.1抗体的大鼠诱发了血管溶血性肾小球损伤。到第3天,受损的肾小球发生了弥漫性血管扩张和节段性微动脉瘤性扩张,并降低了内皮细胞的数量。此后,在第5天至第3周出现组织学增殖性GN。内皮细胞增殖在第1天开始,并在第5天达到峰值,在第7天,肾小球内皮细胞的数量增加并超过了对照值,发生了血管生成性肾小球毛细血管修复。不仅通过毛细血管动脉瘤病变中剩余内皮细胞的毛细血管再生过程,而且还通过第7天从肾小球血管极产生新的毛细血管生长。到第3周,肾小球毛细血管腔的数量也增加到对照水平。随后,肾小球系膜增生性GN消退,大多数肾小球在第4-6周恢复毛细血管网络,恢复其正常结构。在肾小球毛细血管修复过程中,在第7天到第10天之间轻度内皮细胞高细胞活动期间,肾小球内皮细胞显着凋亡(0.06 +/- 0.02凋亡的内皮细胞/肾小球横截面,对照组为0.00 +/- 0.00 ,平均+/- SEM; p <0.05。在Thy-1 GN中,大多数受损的肾小球通过血管生成性毛细血管修复得以恢复,但在10-30%的肾小球中仍存在节段性硬化性瘢痕病变,肾小球毛细血管修复不完全因此,可以得出结论,随着GN中肾小球毛细血管网络的破坏,血管生成性毛细血管修复在受损肾小球的恢复中起着至关重要的作用,毛细血管修复不完全会导致受损肾小球中的硬化性瘢痕病变。剩余内皮细胞产生毛细血管再生的过程,以及肾小球血管极产生新的肾小球毛细血管生长的过程。肾小球毛细血管修复中,凋亡是调节内在内皮细胞数量所必需的。

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