Chiu J, Drummond K N
Am J Pathol. 1972 Aug;68(2):391-406.
Glomerular sialoprotein (GSP) in nephrotoxic nephritis (NTN) rats was studied by chemical and histochemical methods at 1 to 2 hours, 48 hours, 10 days and 16 days after the induction of the disease by intravenous injection of rabbit antiserum to whole rat glomeruli. Histochemically, GSP was demonstrated by the CI and AB 8 GX stains. After the specimen was taken for histologic studies, the glomeruli from the kidneys of each rat were isolated by differential seiving and centrifugation. Quantitative determination of the glomerular sialic acid content from each rat was done using a combination of the chromatographic method of Svennerholm and the thiobarbituric acid assay of Warren. In normal rats the GSP is seen on the epithelial aspect of the glomerular basement membrane (GBM). Within 1 to 2 hours after induction of NTN, disruptuin of the normal membranous distribution of GSP and its dispersion into the mesangial space or the epithelial cytoplasm was noted. Reduction in the amount of staining was also observed after 48 hours. These changes increased in severity as the histologic lesions progressed. A quantitative decrease in glomerular sialic acid became apparent 10 days after the onset of NTN and was still observed at 16 days. Since GSP is situated at the filtration barrier site and is considered a major component of the glomerular antigenic structure, its changes in NTN suggest that it may play an important role in the pathogenesis of this disease and in the alteration of GBM permeability.
通过化学和组织化学方法,对静脉注射兔抗大鼠全肾小球抗血清诱导的肾毒性肾炎(NTN)大鼠在发病后1至2小时、48小时、10天和16天的肾小球涎蛋白(GSP)进行了研究。组织化学上,GSP通过CI和AB 8 GX染色显示。在取标本进行组织学研究后,通过差速筛分和离心从每只大鼠的肾脏中分离出肾小球。使用Svennerholm的色谱法和Warren的硫代巴比妥酸测定法相结合的方法,对每只大鼠的肾小球唾液酸含量进行了定量测定。在正常大鼠中,GSP可见于肾小球基底膜(GBM)的上皮面。在诱导NTN后1至2小时内,注意到GSP正常膜性分布的破坏及其向系膜间隙或上皮细胞质的弥散。48小时后也观察到染色量减少。随着组织学病变的进展,这些变化的严重程度增加。NTN发病10天后,肾小球唾液酸定量减少明显,16天时仍可观察到。由于GSP位于滤过屏障部位,被认为是肾小球抗原结构的主要成分,其在NTN中的变化表明它可能在该疾病的发病机制和GBM通透性改变中起重要作用。