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MicroRNA-378 通过抑制肠黏膜细胞凋亡的机制来防止肠缺血/再灌注损伤。

MicroRNA-378 protects against intestinal ischemia/reperfusion injury via a mechanism involving the inhibition of intestinal mucosal cell apoptosis.

机构信息

Department of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 China.

Department of Anesthesiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.

出版信息

Cell Death Dis. 2017 Oct 12;8(10):e3127. doi: 10.1038/cddis.2017.508.

DOI:10.1038/cddis.2017.508
PMID:29022896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5682673/
Abstract

Intestinal ischemia/reperfusion (I/R) injury remains a major clinical event and contributes to high morbidity and mortality rates, but the underlying mechanisms remain elusive. Recent studies have demonstrated that microRNAs (miRNAs) have important roles in organ I/R injury, but the changes and potential roles of miRNAs in intestinal I/R-induced intestinal injury are unclear. This study was designed to analyze the miRNA expression profiles in intestinal mucosa after I/R injury and to explore the role of target miRNA during this process. Using miRNA microarray analysis, we found changes of 19 miRNAs from the expression profile of miRNAs in a mouse model of intestinal I/R and further verified them by RT-qPCR. Here, we report that miR-378 is one of the markedly decreased miRNAs and found the putative target mRNA that is linked to cell death after applying the TargetScan, miRanda, CLIP-Seq and miRDB prediction algorithms. Our results show that the overexpression of miR-378 significantly ameliorated intestinal tissue damage in wild-type and transgenic mice and oxygen glucose deprivation/reperfusion-challenged IEC-6 cell injury. Moreover, miR-378 overexpression reduced intestinal epithelial cell apoptosis in both in vivo and in vitro ischemic models and attenuated cleaved caspase-3 expression. Collectively, our results revealed that the suppression of caspase-3 activation by miRNA-378 overexpression may be involved in the protective effects of intestinal ischemic damage. MiRNA-378 may serve as a key regulator and therapeutic target in intestinal I/R injury.

摘要

肠缺血/再灌注(I/R)损伤仍然是一个主要的临床事件,导致高发病率和死亡率,但潜在的机制仍不清楚。最近的研究表明,microRNAs(miRNAs)在器官 I/R 损伤中具有重要作用,但 miRNA 在肠 I/R 诱导的肠损伤中的变化和潜在作用尚不清楚。本研究旨在分析 I/R 损伤后肠黏膜中的 miRNA 表达谱,并探讨靶 miRNA 在这一过程中的作用。通过 miRNA 微阵列分析,我们发现了一种小鼠肠 I/R 模型中 miRNA 表达谱的 19 个 miRNA 的变化,并通过 RT-qPCR 进一步验证了这些变化。在这里,我们报告 miR-378 是明显下调的 miRNA 之一,并通过 TargetScan、miRanda、CLIP-Seq 和 miRDB 预测算法找到了与细胞死亡相关的假定靶 mRNA。我们的结果表明,miR-378 的过表达显著改善了野生型和转基因小鼠的肠组织损伤和氧葡萄糖剥夺/再灌注挑战的 IEC-6 细胞损伤。此外,miR-378 的过表达减少了两种体内和体外缺血模型中的肠上皮细胞凋亡,并减弱了 cleaved caspase-3 的表达。总之,我们的结果表明,miR-378 过表达抑制 caspase-3 激活可能参与了肠缺血损伤的保护作用。miRNA-378 可能作为肠 I/R 损伤的关键调节因子和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/8e4fc5de98f7/cddis2017508f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/b08e683c3c31/cddis2017508f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/15bed7de2e61/cddis2017508f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/d114a2c98a1f/cddis2017508f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/347239613d22/cddis2017508f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/8e4fc5de98f7/cddis2017508f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/b08e683c3c31/cddis2017508f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/15bed7de2e61/cddis2017508f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/d114a2c98a1f/cddis2017508f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/347239613d22/cddis2017508f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88c7/5682673/8e4fc5de98f7/cddis2017508f5.jpg

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J Cell Mol Med. 2017 Mar;21(3):432-443. doi: 10.1111/jcmm.12987. Epub 2016 Sep 28.
2
Remifentanil preconditioning protects the small intestine against ischemia/reperfusion injury via intestinal δ- and μ-opioid receptors.瑞芬太尼预处理通过肠道δ和μ阿片受体保护小肠免受缺血/再灌注损伤。
Surgery. 2016 Feb;159(2):548-59. doi: 10.1016/j.surg.2015.07.028. Epub 2015 Sep 26.
3
Predicting effective microRNA target sites in mammalian mRNAs.
Integrative genome-scale analyses reveal post-transcriptional signatures of early human small intestinal development in a directed differentiation organoid model.整合基因组规模分析揭示了定向分化类器官模型中早期人类小肠发育的转录后特征。
BMC Genomics. 2023 Oct 26;24(1):641. doi: 10.1186/s12864-023-09743-1.
4
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Nat Commun. 2023 Sep 6;14(1):5437. doi: 10.1038/s41467-023-41147-3.
5
Gut microbe-derived milnacipran enhances tolerance to gut ischemia/reperfusion injury.肠道微生物衍生的米那普仑增强了对肠道缺血/再灌注损伤的耐受性。
Cell Rep Med. 2023 Mar 21;4(3):100979. doi: 10.1016/j.xcrm.2023.100979.
6
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5
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7
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8
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9
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