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首页> 外文期刊>Histochemistry and cell biology >Semiautomated quantitative image analysis of glomerular immunohistochemistry markers desmin, vimentin, podocin, synaptopodin and WT-1 in acute and chronic rat kidney disease models
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Semiautomated quantitative image analysis of glomerular immunohistochemistry markers desmin, vimentin, podocin, synaptopodin and WT-1 in acute and chronic rat kidney disease models

机译:急性和慢性大鼠肾脏疾病模型中肾小球免疫组化标志物desmin,波形蛋白,podocin,synaptopodin和WT-1的半自动定量图像分析

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Five different glomerular immunohistochemistry markers were evaluated and compared in four different acute and chronic rat kidney disease models. Progression of glomerular or podocyte damage was shown in the puromycin aminonucleoside nephrosis (PAN) and Zucker fatty/spontaneously hypertensive heart failure F1 hybrid (ZSF1) rat model. Progression and prevention of glomerular damage was demonstrated in the Zucker diabetic fatty (ZDF) and Dahl salt-sensitive (Dahl SS) rat. Immunohistochemistry was performed for desmin, vimentin, podocin, synaptopodin and Wilms tumor protein-1 (WT-1), and evaluation of glomerular immunohistochemistry markers was done by semiautomated quantitative image analysis. We found desmin and WT-1 as the most sensitive markers for podocyte damage in both acute and chronic glomerular damage followed by vimentin, podocin and synaptopodin. We were able to demonstrate that early podocyte damage as shown by increased desmin and vimentin staining together with either a phenotypic podocyte change or podocyte loss (reduced numbers of WT-1-stained podocytes) drives the progression of glomerular damage. This is followed by a reduction in podocyte-specific proteins such as podocin and synaptopodin. Our report describes the different sensitivity of glomerular or podocyte markers and gives future guidance for the selection of the most sensitive markers for efficacy testing of new drugs as well as for the selection of tissue-based toxicity markers for glomerular or podocyte injury. In addition to functional clinical chemistry markers, desmin and WT-1 immunohistochemistry offers reliable and valuable data on the morphologic state of podocytes.
机译:在四种不同的急性和慢性大鼠肾脏疾病模型中评估并比较了五种不同的肾小球免疫组织化学标记物。在嘌呤霉素氨基核苷肾病(PAN)和Zucker脂肪/自发性高血压心力衰竭F1杂种(ZSF1)大鼠模型中显示了肾小球或足细胞损伤的进展。在Zucker糖尿病脂肪(ZDF)和Dahl盐敏感性(Dahl SS)大鼠中证明了肾小球损害的进展和预防。对结蛋白,波形蛋白,podocin,突触足蛋白和Wilms肿瘤蛋白-1(WT-1)进行了免疫组织化学,并通过半自动定量图像分析对肾小球免疫组织化学标记物进行了评估。我们发现desmin和WT-1是在急性和慢性肾小球损伤中紧随其后的波形蛋白,podocin和synaptopodin的足细胞损伤最敏感的标志物。我们能够证明,结节蛋白和波形蛋白染色增加以及表型足细胞变化或足细胞丢失(WT-1染色足细胞数量减少)所显示的早期足细胞损伤驱动肾小球损害的进展。随后减少了足细胞特异性蛋白(如Podocin和Synaptopodin)。我们的报告描述了肾小球或足细胞标志物的不同敏感性,并为选择最敏感的标志物提供了指导,以用于新药的功效测试,以及选择基于组织的肾小球或足细胞损伤的毒性标志物。除功能性临床化学标记外,结蛋白和WT-1免疫组织化学还提供了有关足细胞形态状态的可靠且有价值的数据。

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