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从肠道缺血/再灌注损伤的小鼠模型的肠道组织中分离细胞外囊泡。

Isolation of extracellular vesicles from intestinal tissue in a mouse model of intestinal ischemia/reperfusion injury.

机构信息

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

出版信息

Biotechniques. 2020 May;68(5):257-262. doi: 10.2144/btn-2019-0159. Epub 2020 Feb 24.

Abstract

Extracellular vesicles (EVs) are small membranous particles that contribute to intercellular communications. Separating EVs from tissue is still a technical challenge. Here, we present a rigorous method for extracting EVs from intestinal tissue in a mouse intestinal ischemia/reperfusion (I/R) model, and for analyzing their miRNA content. The isolated EVs show a typical cup shape with a size peak of 120-130 nm in diameter, confirmed by TEM and NTA. They also express EV markers such as CD9, CD63, CD81, Tsg101 and Alix. Real-time qPCR confirmed that these pellets contain miRNAs related to I/R injury. Our study presents a practical way to isolate EVs from intestinal tissue which is suitable for downstream applications such as miRNA analysis, and provides a novel method for investigating the mechanism of intestinal I/R injury.

摘要

细胞外囊泡 (EVs) 是一种能够促进细胞间通讯的微小膜性颗粒。从组织中分离 EVs 仍然是一个技术挑战。在这里,我们提出了一种从肠道缺血再灌注(I/R)模型的小鼠肠道组织中提取 EVs 并分析其 miRNA 含量的严格方法。分离的 EVs 通过 TEM 和 NTA 证实呈典型的杯状,直径大小的峰值为 120-130nm。它们还表达 EV 标志物,如 CD9、CD63、CD81、Tsg101 和 Alix。实时 qPCR 证实这些沉淀中含有与 I/R 损伤相关的 miRNA。我们的研究提出了一种从肠道组织中分离 EVs 的实用方法,适用于 miRNA 分析等下游应用,并为研究肠道 I/R 损伤的机制提供了一种新方法。

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