首页> 外文期刊>The Journal of Urology >Expression of osteopontin in rat kidneys: induction during ethylene glycol induced calcium oxalate nephrolithiasis.
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Expression of osteopontin in rat kidneys: induction during ethylene glycol induced calcium oxalate nephrolithiasis.

机译:骨桥蛋白在大鼠肾脏中的表达:在乙二醇诱导的草酸钙肾结石症中诱导。

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PURPOSE: Osteopontin is a well-known component of stone matrix and a strong inhibitor of the nucleation, growth and aggregation of calcium oxalate crystals in vitro. To understand its involvement in vivo in calcium oxalate nephrolithiasis we investigated the renal expression and urinary excretion of osteopontin in normal rats, and rats with hyperoxaluria and calcium oxalate crystal deposits in the kidneys. MATERIALS AND METHODS: Calcium oxalate nephrolithiasis was induced by administering ethylene glycol. Immunohistochemistry and in situ hybridization were done to localize osteopontin and osteopontin messenger RNA in the kidneys, while sensitive reverse transcriptase quantitative competitive template polymerase chain reaction was performed to detect and quantify osteopontin messenger RNA expression. Urinary excretion was determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blot analysis, and then quantified by densitometry of the Western blots. RESULTS: Osteopontin expression in the kidneys was significantly increased after hyperoxaluria and it increased further after the deposition of calcium oxalate crystals in the kidneys. Urinary excretion of osteopontin increased concomitantly. The results reveal differences in renal responses after exposure to oxalate and calcium oxalate crystals. In normal kidneys osteopontin expression was limited to a small number of cells of the thin limbs of the loop of Henle and papillary surface epithelium. During hyperoxaluria osteopontin expression in the kidneys was increased but still mostly limited to cells of the thin limb and papillary surface epithelium. However, after calcium oxalate crystal deposition osteopontin expression was observed throughout the kidneys, including segments of the proximal tubules. CONCLUSIONS: In response to exposure to oxalate and calcium oxalate crystals renal epithelial cells increase the production of osteopontin, which may have a significant role in calcium oxalate nephrolithiasis.
机译:目的:骨桥蛋白是石材基质的众所周知成分,并且是体外草酸钙晶体成核,生长和聚集的强抑制剂。为了了解其在体内参与草酸钙肾结石的形成,我们调查了正常大鼠以及高草酸尿症和草酸钙晶体沉积在肾脏中的大鼠的肾脏表达和骨桥蛋白的尿排泄。材料与方法:乙二醇诱导草酸钙肾结石病。进行了免疫组织化学和原位杂交以在肾脏中定位骨桥蛋白和骨桥蛋白信使RNA,同时进行了敏感的逆转录酶定量竞争模板聚合酶链反应以检测和定量骨桥蛋白信使RNA的表达。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和蛋白质印迹分析确定尿排泄,然后通过蛋白质印迹的光密度法定量。结果:高草酸尿后肾脏中骨桥蛋白的表达显着增加,草酸钙晶体在肾脏中沉积后,骨桥蛋白的表达进一步增加。骨桥蛋白的尿排泄随之增加。结果揭示了暴露于草酸盐和草酸钙晶体后肾脏反应的差异。在正常肾脏中,骨桥蛋白的表达仅限于Henle环和乳头表面上皮的四肢细小细胞。在高草酸尿症期间,肾脏中骨桥蛋白的表达增加,但仍主要限于瘦肢和乳头表面上皮细胞。但是,在草酸钙晶体沉积后,整个肾脏(包括近端小管的各个部分)都观察到了骨桥蛋白的表达。结论:响应于草酸和草酸钙晶体的暴露,肾上皮细胞增加骨桥蛋白的产生,这可能在草酸钙肾结石症中具有重要作用。

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