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正常大鼠和糖尿病大鼠肾小球壁内源性免疫球蛋白G的超微结构分布

Ultrastructural distribution of endogenous IgGs in the glomerular wall of control and diabetic rats.

作者信息

Desjardins M, Bendayan M

机构信息

Department d'Anatomie, Université de Montréal, Québec, Canada.

出版信息

Histochem J. 1989 Dec;21(12):731-42. doi: 10.1007/BF01002839.

Abstract

Endogenous IgG molecules were revealed with high resolution EM over the glomerular wall in renal tissues sampled from short and longterm control and streptozotocin induced diabetic rats by applying the protein A-gold immunocytochemical approach. In tissues from control animals, IgG antigenic sites were revealed on the subendothelial side of the basement membrane, the epithelial side being only weakly labelled. In contrast, in longterm diabetic animals IgG antigenic sites were present throughout the entire thickness of the basement membrane, and in patches closely associated with the plasma membrane of the epithelial cells. Deposits of basement membrane-like material present in the mesangial area were also highly labelled for IgG. Numerous intensely labelled lysosome-like structures were present in the epithelial cells. Morphometrical evaluation of the distribution of the labelling over the basement membrane confirmed these observations. In control animals a peak of labelling was found at 30 nm from the endothelial cell region corresponding to the subendothelial side of the lamina densa. In longterm diabetic animals the labelling was more uniformly distributed throughout the entire thickness of the basement membrane. These data were correlated to biochemical determinations of proteinuria and IgG excretion in urine samples from the control and the diabetic animals. These results suggest that in normal conditions the lamina densa may represent the main barrier for the restriction of the passage of IgGs through the glomerular wall. Modifications at that level occur during diabetes leading to or participating in the loss of the selective permeability of the basement membrane.

摘要

通过应用蛋白A-金免疫细胞化学方法,在从短期和长期对照以及链脲佐菌素诱导的糖尿病大鼠采集的肾组织中,以高分辨率电子显微镜观察到肾小球壁上的内源性IgG分子。在对照动物的组织中,IgG抗原位点出现在基底膜的内皮下侧,上皮侧仅有微弱标记。相比之下,在长期糖尿病动物中,IgG抗原位点存在于基底膜的整个厚度中,并呈斑块状与上皮细胞质膜紧密相关。系膜区存在的基底膜样物质沉积物也被高度标记为IgG。上皮细胞中有许多高度标记的溶酶体样结构。对基底膜上标记分布的形态计量学评估证实了这些观察结果。在对照动物中,在距内皮细胞区域30 nm处发现标记峰值,对应于致密层的内皮下侧。在长期糖尿病动物中,标记更均匀地分布在基底膜的整个厚度中。这些数据与对照和糖尿病动物尿液样本中蛋白尿和IgG排泄的生化测定相关。这些结果表明,在正常情况下,致密层可能是限制IgG通过肾小球壁的主要屏障。糖尿病期间该水平发生改变,导致或参与基底膜选择性通透性的丧失。

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