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用于检测正常肾小球以及特发性和实验性肾病中阴离子位点的聚-L-赖氨酸-金探针。一项比较超微结构研究。

Poly-L-lysine-gold probe for the detection of anionic sites in normal glomeruli and in idiopathic and experimentally-induced nephrosis. A comparative ultrastructural study.

作者信息

Russo P, Gingras D, Bendayan M

机构信息

Département de Pathologie, Hôpital Ste-Justine, Montréal, Québec, Canada.

出版信息

Am J Pathol. 1993 Jan;142(1):261-71.

PMID:8424459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1886853/
Abstract

Anionic sites play a key role in the charge selectivity of glomerular filtration as well as in the maintenance of the structural integrity of the visceral epithelium and podocytes. Alterations in these sites are believed to be a major factor underlying human idiopathic nephrosis and puromycin-nephrosis in the rat. The poly-L-lysine-gold complex was used for the ultrastructural detection of anionic sites in renal glomeruli of patients with idiopathic nephrosis as well as of rats with puromycin-induced nephrosis, allowing for study of the changes occurring in the anionic sites during nephrosis and for the comparison between human disease and this experimental model. In both normal human and rat controls, the probe was detected on epithelial and endothelial cell surfaces and on the glomerular basement membrane, mainly in both laminae rarae. In proteinuric rats, a decrease in labeling intensity was noted on podocyte membranes and in the lamina rara externa, with a corresponding increase in the more central areas of the glomerular basement membrane. These changes were not as evident in proteinuric humans. Furthermore, a reduction in labeling density was noted in the glomerular basement membrane of proteinuric animals, although this could not be substantiated in human tissues. Poly-L-lysine-gold is a useful probe for anionic sites in fixed tissues, and allows for comparison between human disease and its experimental counterpart.

摘要

阴离子位点在肾小球滤过的电荷选择性以及脏层上皮和足细胞结构完整性的维持中起关键作用。这些位点的改变被认为是人类特发性肾病和大鼠嘌呤霉素肾病的主要潜在因素。聚-L-赖氨酸-金复合物用于特发性肾病患者以及嘌呤霉素诱导肾病大鼠的肾小球中阴离子位点的超微结构检测,从而能够研究肾病期间阴离子位点发生的变化,并对人类疾病与该实验模型进行比较。在正常人类和大鼠对照中,探针主要在两个透明层中检测到上皮和内皮细胞表面以及肾小球基底膜上。在蛋白尿大鼠中,足细胞膜和外透明层的标记强度降低,而肾小球基底膜更中央区域的标记强度相应增加。这些变化在蛋白尿人类中不那么明显。此外,蛋白尿动物的肾小球基底膜标记密度降低,尽管在人体组织中无法证实这一点。聚-L-赖氨酸-金是固定组织中阴离子位点的有用探针,并允许对人类疾病与其实验对应物进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/a3ab5ddc081f/amjpathol00073-0264-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/05bfca5974dc/amjpathol00073-0261-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/eb7eced0a1df/amjpathol00073-0262-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/c4794d57bff2/amjpathol00073-0263-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/69c3fe34c7f7/amjpathol00073-0263-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/a3ab5ddc081f/amjpathol00073-0264-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/05bfca5974dc/amjpathol00073-0261-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/eb7eced0a1df/amjpathol00073-0262-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/c4794d57bff2/amjpathol00073-0263-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/69c3fe34c7f7/amjpathol00073-0263-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea47/1886853/a3ab5ddc081f/amjpathol00073-0264-a.jpg

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本文引用的文献

1
Size and charge selective permeability defects induced in glomerular basement membrane by a polycation.一种聚阳离子在肾小球基底膜中诱导产生的大小和电荷选择性通透性缺陷
Kidney Int. 1984 Jan;25(1):11-9. doi: 10.1038/ki.1984.2.
2
Increased permeability of the glomerular basement membrane to ferritin after removal of glycosaminoglycans (heparan sulfate) by enzyme digestion.通过酶消化去除糖胺聚糖(硫酸乙酰肝素)后,肾小球基底膜对铁蛋白的通透性增加。
J Cell Biol. 1980 Aug;86(2):688-93. doi: 10.1083/jcb.86.2.688.
3
Heparan sulfate--rich anionic sites in the human glomerular basement membrane. Decreased concentration in congenital nephrotic syndrome.
人肾小球基底膜中富含硫酸乙酰肝素的阴离子位点。先天性肾病综合征中浓度降低。
N Engl J Med. 1983 Oct 27;309(17):1001-9. doi: 10.1056/NEJM198310273091701.
4
Loss of heparan sulfate proteoglycan from glomerular basement membrane of nephrotic rats.肾病大鼠肾小球基底膜硫酸乙酰肝素蛋白聚糖的缺失
Lab Invest. 1983 Mar;48(3):292-302.
5
Minimal change nephropathy: an electrochemical disorder of the glomerular membrane.微小病变性肾病:肾小球膜的一种电化学紊乱。
Am J Med. 1981 Feb;70(2):262-8. doi: 10.1016/0002-9343(81)90760-9.
6
Glomerular sialic acid and proteinuria in human renal disease.人类肾脏疾病中的肾小球唾液酸与蛋白尿
Lab Invest. 1973 Apr;28(4):477-81.
7
Mucosubstances of the glomerulus.肾小球的黏液物质。
Lab Invest. 1969 Aug;21(2):119-25.
8
Glomerular polyanion. Alteration in aminonucleoside nephrosis.肾小球多阴离子。氨基核苷肾病中的改变。
Lab Invest. 1970 Dec;23(6):649-57.
9
Localization of sialic acid in kidney glomeruli: regionalization in the podocyte plasma membrane and loss in experimental nephrosis.唾液酸在肾小球中的定位:足细胞质膜中的区域化及在实验性肾病中的缺失
Proc Natl Acad Sci U S A. 1985 Dec;82(24):8508-12. doi: 10.1073/pnas.82.24.8508.
10
Glomerular epithelial abnormalities associated with the onset of proteinuria in aminonucleoside nephrosis.氨基核苷肾病中与蛋白尿发生相关的肾小球上皮异常。
Am J Pathol. 1987 Feb;126(2):220-9.