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足细胞损伤会加重系膜增生性肾小球肾炎。

Podocyte injuries exacerbate mesangial proliferative glomerulonephritis.

作者信息

Morioka Y, Koike H, Ikezumi Y, Ito Y, Oyanagi A, Gejyo F, Shimizu F, Kawachi H

机构信息

Department of Cell Biology, Institute of Nephrology, Faculty of Medicine, Niigata University, Japan.

出版信息

Kidney Int. 2001 Dec;60(6):2192-204. doi: 10.1046/j.1523-1755.2001.00047.x.

Abstract

BACKGROUND

From the observations of morphology seen in early phases of the experimental models of the irreversible mesangial proliferative glomerulonephritis, we hypothesized that podocyte injury is one of the important factors in bringing upon irreversible glomerular alterations. To verify this hypothesis, we investigated whether podocyte injury induced by puromycin aminonucleoside (PAN) injection affects the mesangial alterations of anti-Thy 1.1 glomerulonephritis.

METHODS

Female Wistar rats were injected with 0.5 mg monoclonal antibody (mAb) 1-22-3 five days after the injection of 10 mg or 5 mg/100 g body weight (BW) of puromycin aminonucleoside (PAN), and sacrificed at 7 days or 8 weeks after the mAb 1-22-3 injection.

RESULTS

Consecutive injections of 10 mg/100 g BW of PAN and mAb 1-22-3 caused the irreversible mesangial alteration with persistent proteinuria (at week 8, proteinuria 100.3 +/- 57.8 mg/24 h, matrix score 1.13 +/- 0.52, collagen type I score 2.04 +/- 0.53, mRNA for collagen type I 227 +/- 79% to the group with a single injection of 1-22-3). Although single injection of 5 mg/100 g BW of PAN was not capable of inducing abnormal proteinuria, consecutive injections of 5 mg/100 g BW of PAN and mAb 1-22-3 also caused irreversible mesangial alteration and persistent proteinuria.

CONCLUSIONS

Podocyte injury might be an important factor that exacerbates mesangial proliferation and mesangial matrix expansion. The irreversible mesangial alterations caused by consecutive injections of PAN and mAb 1-22-3 may be a novel model that could be used to analyze the mechanism of progressive mesangial alteration.

摘要

背景

从不可逆性系膜增生性肾小球肾炎实验模型早期阶段的形态学观察中,我们推测足细胞损伤是导致不可逆性肾小球改变的重要因素之一。为验证这一假设,我们研究了嘌呤霉素氨基核苷(PAN)注射诱导的足细胞损伤是否会影响抗Thy 1.1肾小球肾炎的系膜改变。

方法

雌性Wistar大鼠在注射10 mg或5 mg/100 g体重(BW)的嘌呤霉素氨基核苷(PAN)5天后,注射0.5 mg单克隆抗体(mAb)1-22-3,并在注射mAb 1-22-3后7天或8周处死。

结果

连续注射10 mg/100 g BW的PAN和mAb 1-22-3导致不可逆性系膜改变及持续性蛋白尿(第8周时,蛋白尿为100.3±57.8 mg/24 h,基质评分1.13±0.52,I型胶原评分2.04±0.53,I型胶原mRNA为单次注射1-22-3组的227±79%)。虽然单次注射5 mg/100 g BW的PAN不能诱导异常蛋白尿,但连续注射5 mg/100 g BW的PAN和mAb 1-22-3也会导致不可逆性系膜改变及持续性蛋白尿。

结论

足细胞损伤可能是加剧系膜增生和系膜基质扩张的重要因素。连续注射PAN和mAb 1-22-3所导致的不可逆性系膜改变可能是一种可用于分析进行性系膜改变机制的新型模型。

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