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足细胞损伤在肾小球硬化和肾小管间质病变发病机制中的作用:在进行性肾病生长激素转基因小鼠模型中的发现

[Role of podocyte damage in the pathogenesis of glomerulosclerosis and tubulointerstitial lesions: findings in the growth hormone transgenic mouse model of progressive nephropathy].

作者信息

Wanke R, Wolf E, Brem G, Hermanns W

机构信息

Institut für Tierpathologie, Universität München.

出版信息

Verh Dtsch Ges Pathol. 2001;85:250-6.

Abstract

The sequence of structural changes terminating in glomerulosclerosis, tubular atrophy and interstitial fibrosis was analyzed in the growth hormone (GH) transgenic mouse (TM) model of progressive renal disease. The investigation was performed in TM expressing the bovine GH gene under the control of the murine metallothionein-1-promoter and non-transgenic controls (CM) of different age groups. The kidneys were studied by light microscopy, transmission and scanning electron microscopy, and were analyzed with stereological methods. Early-stage renal lesions were characterized by glomerular hypertrophy and mesangial expansion. In 7-week-old TM the mean glomerular volume was twice that of age-matched CM. The number of endothelial and of mesangial cells per glomerulus was increased in TM vs. CM, while the number of podocytes did not change. The podocytes demonstrated hypertrophy and foot process effacement. Concomitant with an age-related further increase of glomerular size in TM, severe maladaptive podocyte lesions including detachment of podocytes were observed. The resultant denudation of the glomerular basement membrane was associated with severe proteinuria, glomerular hyalinosis, synechia formation and collapse of glomerular capillaries. These lesions progressed to glomerular obsolescence that was associated with atrophy of the adjacent tubule and interstitial fibrosis. The progressive kidney lesions in this model appear to be attributable to a considerable extent to podocyte damage resulting from the limited capacity of this cell type to keep up with progressing overall tuft growth. The findings provide further evidence that mature podocytes are unable for effective cell replication in vivo, and that podocyte damage plays a significant role in the pathogenesis of progressive glomerulosclerosis with tubular atrophy and interstitial fibrosis.

摘要

在进行性肾病的生长激素(GH)转基因小鼠(TM)模型中,分析了以肾小球硬化、肾小管萎缩和间质纤维化为终点的结构变化序列。研究在由小鼠金属硫蛋白-1启动子控制表达牛GH基因的TM以及不同年龄组的非转基因对照(CM)中进行。通过光学显微镜、透射电子显微镜和扫描电子显微镜对肾脏进行研究,并用体视学方法进行分析。早期肾脏病变的特征为肾小球肥大和系膜扩张。在7周龄的TM中,平均肾小球体积是年龄匹配的CM的两倍。与CM相比,TM中每个肾小球的内皮细胞和系膜细胞数量增加,而足细胞数量未改变。足细胞表现出肥大和足突消失。随着TM中肾小球大小随年龄进一步增加,观察到严重的适应性不良足细胞病变,包括足细胞脱离。由此导致的肾小球基底膜剥脱与严重蛋白尿、肾小球玻璃样变性、粘连形成和肾小球毛细血管塌陷有关。这些病变进展为肾小球荒废,伴有相邻肾小管萎缩和间质纤维化。该模型中进行性肾脏病变在很大程度上似乎归因于足细胞损伤,这是由于这种细胞类型跟上整个肾小球丛进展性生长的能力有限所致。这些发现进一步证明成熟足细胞在体内无法进行有效的细胞复制,并且足细胞损伤在伴有肾小管萎缩和间质纤维化的进行性肾小球硬化的发病机制中起重要作用。

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