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肾足蛋白报告基因小鼠的建立及其在化学筛选中的应用。

Establishment of Nephrin Reporter Mice and Use for Chemical Screening.

作者信息

Tsuchida Junichi, Matsusaka Taiji, Ohtsuka Masato, Miura Hiromi, Okuno Yukiko, Asanuma Katsuhiko, Nakagawa Takahiko, Yanagita Motoko, Mori Kiyoshi

机构信息

TMK Project, Medical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Research Unit/Nephrological & Endocrinological Science, Sohyaku, Innovative Research Division, Mitsubishi Tanabe Pharma Corporation, Toda, Saitama, Japan.

出版信息

PLoS One. 2016 Jun 30;11(6):e0157497. doi: 10.1371/journal.pone.0157497. eCollection 2016.

Abstract

Nephrin is a critical component of glomerular filtration barrier, which is important to maintain glomerular structure and avoid proteinuria. Downregulation of nephrin expression is commonly observed at early stage of glomerular disorders, suggesting that methods to increase nephrin expression in podocytes may have therapeutic utility. Here, we generated a knockin mouse line carrying single copy of 5.5 kb nephrin promoter controlling expression of enhanced green fluorescent protein (EGFP) at Rosa26 genomic locus (Nephrin-EGFP mouse). In these mice, EGFP was specifically expressed in podocytes. Next, we isolated and cultivated glomeruli from these mice, and developed a protocol to automatically quantitate EGFP expression in cultured glomeruli. EGFP signal was markedly reduced after 5 days of culture but reduction was inhibited by vitamin D treatment. We confirmed that vitamin D increased mRNA and protein expression of endogenous nephrin in cultivated glomeruli. Thus, we generated a mouse line converting nephrin promoter activity into fluorescence, which can be used to screen compounds having activity to enhance nephrin gene expression.

摘要

Nephrin是肾小球滤过屏障的关键组成部分,对维持肾小球结构和避免蛋白尿至关重要。在肾小球疾病早期通常会观察到Nephrin表达下调,这表明增加足细胞中Nephrin表达的方法可能具有治疗作用。在此,我们构建了一种敲入小鼠品系,其在Rosa26基因组位点携带单拷贝5.5 kb Nephrin启动子,用于控制增强型绿色荧光蛋白(EGFP)的表达(Nephrin-EGFP小鼠)。在这些小鼠中,EGFP在足细胞中特异性表达。接下来,我们从这些小鼠中分离并培养肾小球,并开发了一种自动定量培养肾小球中EGFP表达的方案。培养5天后,EGFP信号明显降低,但维生素D处理可抑制这种降低。我们证实维生素D可增加培养肾小球中内源性Nephrin的mRNA和蛋白表达。因此,我们构建了一种将Nephrin启动子活性转化为荧光的小鼠品系,可用于筛选具有增强Nephrin基因表达活性的化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dad6/4928931/24282ac6b289/pone.0157497.g001.jpg

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