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在缺乏主要尿蛋白的小鼠中进行尿蛋白分析。

Urinary protein analysis in mice lacking major urinary proteins.

机构信息

Laboratory of Animal Models for Human Diseases, National Institutes of Biomedical Innovation, Health and Nutrition, 7-6-8 Saito-Asagi, Ibaraki, Osaka 568-0085, Japan.

出版信息

Exp Anim. 2021 Aug 6;70(3):406-411. doi: 10.1538/expanim.21-0010. Epub 2021 Apr 20.

DOI:10.1538/expanim.21-0010
PMID:33883349
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8390313/
Abstract

Mouse urine contains major urinary proteins (MUPs) that are not found in human urine. Therefore, even healthy mice exhibit proteinuria, unlike healthy humans, making it challenging to use mice as models for human diseases. It was also unknown whether dipsticks for urinalysis could measure protein concentrations precisely in urine containing MUPs. To resolve these problems, we produced MUP-knockout (Mup-KO) mice by removing the Mup gene cluster using Cas9 proteins and two guide RNAs and characterized the urinary proteins in these mice. We measured the urinary protein concentrations in Mup-KO and wild-type mice using a protein quantitation kit and dipsticks. We also examined the urinary protein composition using SDS-PAGE and two-dimensional electrophoresis (2DE). The urinary protein concentration was significantly lower (P<0.001) in Mup-KO mice (17.9 ± 1.8 mg/dl, mean ± SD, n=3) than in wild-type mice (73.7 ± 8.2 mg/dl, n=3). This difference was not reflected in the dipstick values, perhaps due to the low sensitivity to MUPs. This suggests that dipsticks have limited ability to measure changes in MUPs with precision. SDS-PAGE and 2DE confirmed that Mup-KO mice, like humans, had no MUPs in their urine, whereas wild-type mice had abundant MUPs in their urine. The absence of the masking effect of MUPs in 2DE would enable clear comparisons of urinary proteins, especially low-molecular-weight proteins. Thus, Mup-KO mice may provide a useful model for human urinalysis.

摘要

鼠尿中含有人类尿液中不存在的主要尿蛋白 (MUPs)。因此,即使是健康的小鼠也会出现蛋白尿,与健康人类不同,这使得小鼠难以作为人类疾病的模型。此外,尚不清楚用于尿液分析的试条是否可以精确测量含有 MUPs 的尿液中的蛋白质浓度。为了解决这些问题,我们使用 Cas9 蛋白和两条向导 RNA 去除 Mup 基因簇,产生了 MUP 敲除 (Mup-KO) 小鼠,并对这些小鼠的尿液蛋白进行了特征分析。我们使用蛋白质定量试剂盒和试条测量了 Mup-KO 和野生型小鼠的尿蛋白浓度。我们还使用 SDS-PAGE 和二维电泳 (2DE) 检查了尿蛋白组成。Mup-KO 小鼠的尿蛋白浓度明显较低 (P<0.001) (17.9 ± 1.8 mg/dl,平均值 ± SD,n=3),而野生型小鼠的尿蛋白浓度为 73.7 ± 8.2 mg/dl (n=3)。试条值没有反映出这种差异,这可能是由于对 MUPs 的低灵敏度。这表明试条在精确测量 MUPs 变化方面的能力有限。SDS-PAGE 和 2DE 证实,Mup-KO 小鼠与人类一样,尿液中没有 MUPs,而野生型小鼠尿液中含有丰富的 MUPs。2DE 中不存在 MUPs 的掩蔽效应,这将使尿液蛋白,特别是低分子量蛋白的比较更加清晰。因此,Mup-KO 小鼠可能为人类尿液分析提供有用的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/8390313/9d3878086c77/expanim-70-406-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/8390313/8094aeda146d/expanim-70-406-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/8390313/6deca6b4af35/expanim-70-406-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/8390313/9d3878086c77/expanim-70-406-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/8390313/8094aeda146d/expanim-70-406-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/8390313/6deca6b4af35/expanim-70-406-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4a0/8390313/9d3878086c77/expanim-70-406-g003.jpg

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