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慢病毒介导的HuR RNA干扰通过p38/MK2信号通路对术后肠梗阻的调控

Regulation of Postoperative Ileus by Lentivirus-Mediated HuR RNA Interference via the p38/MK2 Signaling Pathway.

作者信息

Xiong Ye Dao, Rong Lu Xing, Pan Chi

机构信息

Fujian Medical University Union Hospital, Fuzhou, China.

出版信息

J Gastrointest Surg. 2017 Feb;21(2):389-397. doi: 10.1007/s11605-016-3303-z. Epub 2016 Oct 27.

Abstract

OBJECTIVES

The objective of the present study is to explore the effect of lentivirus-mediated HuR interference on the development and progression of postoperative ileus and the role of HuR in the regulation of the p38/MAPK-activated protein kinase-2 (MK2) signaling pathway during postoperative ileus.

METHODS

To establish a mouse model of lentiviral transduction, we first determined the optimum effective titer of lentiviral vectors for transduction of the murine small intestine via the abdominal cavity by using hematoxylin and eosin (HE) staining, immunohistochemistry, detection of GFP messenger RNA (mRNA) and protein, and Western blotting. To investigate the effect of HuR interference on gene expression during postoperative ileus, we established a mouse model of postoperative ileus and used RT-PCR to measure the expression of proinflammatory genes, ELISA to measure the expression of serum inflammatory cytokines, immunohistochemistry to evaluate inflammatory cell infiltration in the small intestine, HE staining of paraffin sections to examine the pathology of the small intestine, and Western blotting to measure HuR expression and identify its role in the regulation of the p38/MK2 inflammatory pathway.

RESULTS

We successfully designed a mouse model of intraperitoneal transduction of HuR-RNAi lentivirus. When HuR gene expression was suppressed in a mouse model of postoperative ileus, the infiltration of inflammatory cells, the expression of proinflammatory genes, and the levels of serum inflammatory cytokines were significantly reduced. This reduction in inflammation correlated with reduced cytoplasmic localization of HuR and reduced activation of MK2.

CONCLUSIONS

Within the p38/MK2 signal transduction pathway, HuR may increase the mRNA stability of various inflammatory cytokines, thereby promoting inflammation that causes postoperative ileus. Suppressing the expression of HuR in a postoperative ileus model can effectively suppress the postoperative ileus inflammatory reaction. HuR might serve as a candidate drug target for the prevention and mitigation of postoperative ileus.

摘要

目的

本研究旨在探讨慢病毒介导的HuR干扰对术后肠梗阻发生发展的影响,以及HuR在术后肠梗阻过程中对p38/丝裂原活化蛋白激酶-2(MK2)信号通路的调控作用。

方法

为建立慢病毒转导小鼠模型,我们首先通过苏木精-伊红(HE)染色、免疫组织化学、绿色荧光蛋白信使核糖核酸(mRNA)和蛋白检测以及蛋白质印迹法,确定慢病毒载体经腹腔转导小鼠小肠的最佳有效滴度。为研究HuR干扰对术后肠梗阻期间基因表达的影响,我们建立了术后肠梗阻小鼠模型,并采用逆转录聚合酶链反应(RT-PCR)检测促炎基因的表达,酶联免疫吸附测定(ELISA)检测血清炎性细胞因子的表达,免疫组织化学评估小肠炎性细胞浸润情况,石蜡切片HE染色检查小肠病理变化,以及蛋白质印迹法检测HuR表达并确定其在p38/MK2炎性信号通路调控中的作用。

结果

我们成功构建了HuR-RNAi慢病毒腹腔转导小鼠模型。在术后肠梗阻小鼠模型中抑制HuR基因表达时,炎性细胞浸润、促炎基因表达及血清炎性细胞因子水平均显著降低。炎症反应的减轻与HuR胞质定位减少及MK2激活降低相关。

结论

在p38/MK2信号转导通路中,HuR可能增加多种炎性细胞因子的mRNA稳定性,从而促进导致术后肠梗阻的炎症反应。在术后肠梗阻模型中抑制HuR表达可有效抑制术后肠梗阻的炎症反应。HuR可能是预防和减轻术后肠梗阻的候选药物靶点。

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