首页> 美国卫生研究院文献>Clinical and Experimental Immunology >Intraglomerular expression of transforming growth factor-beta 1 (TGF-beta 1) mRNA in patients with glomerulonephritis: quantitative analysis by competitive polymerase chain reaction.
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Intraglomerular expression of transforming growth factor-beta 1 (TGF-beta 1) mRNA in patients with glomerulonephritis: quantitative analysis by competitive polymerase chain reaction.

机译:肾小球肾炎患者转化生长因子-β1(TGF-β1)mRNA的肾小球内表达:通过竞争性聚合酶链反应的定量分析。

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摘要

TGF-beta 1 is involved in the pathogenesis of glomerular sclerosis. We studied the intraglomerular expression of TGF-beta 1 mRNA in patients with glomerulonephritis using competitive polymerase chain reaction (PCR). This method is sensitive enough to quantify cDNA copies of mRNA present in small amounts of samples. Renal biopsy specimens were obtained from 42 patients with various kinds of glomerulonephritis. Ten glomeruli were dissected from renal biopsy specimens. Normal glomeruli were also obtained from the resected kidneys of eight patients with renal cell cancer. Total RNA was extracted from the glomeruli and reverse transcribed into cDNA with reverse transcriptase. To prepare samples containing identical amounts of beta-actin cDNA (8 pg), we performed competitive PCR by co-amplifying mutant templates of beta-actin with a unique EcoRI site. Next, to measure TGF-beta 1 cDNA, we performed competitive PCR by co-amplifying mutant templates of TGF-beta 1. We observed a higher glomerular expression of TGF-beta 1 mRNA in cases of mesangial proliferative glomerulonephritis having a moderate increase in mesangial matrix, diabetic nephropathy and diffuse proliferative lupus nephritis, compared with normal glomeruli. Results suggest that the intraglomerular synthesis of TGF-beta 1 may be involved in the progression of glomerulonephritis in humans.
机译:TGF-beta 1参与肾小球硬化的发病机制。我们使用竞争性聚合酶链反应(PCR)研究了肾小球肾炎患者肾小球内TGF-β1mRNA的表达。这种方法足够灵敏,可以定量少量样品中存在的mRNA的cDNA拷贝。肾活检标本取自42例各种肾小球肾炎患者。从肾活检标本中解剖出十个肾小球。还从八名肾细胞癌患者的切除肾脏中获得了正常的肾小球。从肾小球中提取总RNA,并用逆转录酶逆转录成cDNA。为了制备包含相同量的β-肌动蛋白cDNA(8 pg)的样品,我们通过共扩增具有独特EcoRI位点的β-肌动蛋白的突变模板进行了竞争PCR。接下来,为了测量TGF-beta 1 cDNA,我们通过共扩增TGF-beta 1的突变模板进行了竞争性PCR。我们观察到在肾小球膜增生性肾小球肾炎中肾小球膜增生的情况下TGF-beta 1 mRNA的肾小球表达更高与正常肾小球相比,基质,糖尿病性肾病和弥漫性增生性狼疮性肾炎。结果表明,TGF-β1的肾小球内合成可能与人类肾小球肾炎的进展有关。

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