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大鼠急性胰腺炎中胰腺炎相关蛋白的小干扰RNA基因敲低

Small-interference RNA gene knockdown of pancreatitis-associated proteins in rat acute pancreatitis.

作者信息

Lin Yin-Yao, Viterbo Domenico, Mueller Cathy M, Stanek Albert E, Smith-Norowitz Tamar, Drew Hazel, Wadgaonkar Raj, Zenilman Michael E, Bluth Martin H

机构信息

SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.

出版信息

Pancreas. 2008 May;36(4):402-10. doi: 10.1097/MPA.0b013e31815f3933.

Abstract

OBJECTIVES

Pancreatitis-associated proteins (PAPs) are induced in acute pancreatitis and antisense-mediated gene knockdown of PAP decreased PAP gene expression and worsened pancreatitis. Here, we investigated the effect of a more stable inhibition of PAP using small-interference RNA gene knockdown in vitro and in an in vivo model of experimental pancreatitis.

METHODS

Pancreatitis-associated protein-specific siRNA was administered to AR42J cell cultures or rats induced with pancreatitis. Controls included administration of scrambled siRNA or vehicle alone. After 24 hours, cells and pancreata were harvested and assessed for PAP (PAP 1, PAP 2, PAP 3) gene expression and pancreatitis severity.

RESULTS

In vitro, PAP protein, and mRNA levels were reduced (PAP 1, 76%; PAP 2, 8%; PAP 3, 24%) in cells treated with PAP siRNA. In vivo, PAP 1, and PAP 3 expressions were reduced (PAP 1, 36%; PAP 3, 66%) in siRNA-treated rats; there was no difference in PAP 2 isoform mRNA expression and serum protein levels. Serum amylase and lipase levels decreased (> or =50%) after administration of siRNA; interleukin (IL) 1beta, IL-4, and IL-6 increased, whereas C-reactive protein and tumor necrosis factor-alpha decreased when compared with vehicle control. Administration of PAP siRNA correlated with worsening histopathology.

CONCLUSIONS

siRNA-mediated gene knockdown of PAP worsens pancreatitis. Differences in gene knockdown technology may provide different approaches to study gene function.

摘要

目的

胰腺炎相关蛋白(PAPs)在急性胰腺炎中被诱导产生,反义介导的PAP基因敲低可降低PAP基因表达并加重胰腺炎。在此,我们研究了在体外和实验性胰腺炎体内模型中使用小干扰RNA基因敲低对PAP进行更稳定抑制的效果。

方法

将胰腺炎相关蛋白特异性小干扰RNA应用于AR42J细胞培养物或诱导产生胰腺炎的大鼠。对照组包括给予乱序小干扰RNA或仅给予溶剂。24小时后,收获细胞和胰腺并评估PAP(PAP 1、PAP 2、PAP 3)基因表达和胰腺炎严重程度。

结果

在体外,用PAP小干扰RNA处理的细胞中PAP蛋白和mRNA水平降低(PAP 1降低76%;PAP 2降低8%;PAP 3降低24%)。在体内,小干扰RNA处理的大鼠中PAP 1和PAP 3表达降低(PAP 1降低36%;PAP 3降低66%);PAP 2亚型mRNA表达和血清蛋白水平无差异。给予小干扰RNA后血清淀粉酶和脂肪酶水平降低(≥50%);与溶剂对照组相比,白细胞介素(IL)1β、IL - 4和IL - 6增加,而C反应蛋白和肿瘤坏死因子 - α降低。给予PAP小干扰RNA与组织病理学恶化相关。

结论

小干扰RNA介导的PAP基因敲低会加重胰腺炎。基因敲低技术的差异可能为研究基因功能提供不同方法。

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