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细胞外囊泡作为急性器官损伤的介质和标志物:当前概念。

Extracellular vesicles as mediators and markers of acute organ injury: current concepts.

机构信息

Department of Trauma-, Hand- and Reconstructive Surgery, University Hospital Frankfurt, Goethe-University, Frankfurt am Main, Germany.

出版信息

Eur J Trauma Emerg Surg. 2022 Jun;48(3):1525-1544. doi: 10.1007/s00068-021-01607-1. Epub 2021 Feb 3.

Abstract

Due to the continued high incidence and mortality rate worldwide, there is a need to develop new strategies for the quick, precise, and valuable recognition of presenting injury pattern in traumatized and poly-traumatized patients. Extracellular vesicles (EVs) have been shown to facilitate intercellular communication processes between cells in close proximity as well as distant cells in healthy and disease organisms. miRNAs and proteins transferred by EVs play biological roles in maintaining normal organ structure and function under physiological conditions. In pathological conditions, EVs change the miRNAs and protein cargo composition, mediating or suppressing the injury consequences. Therefore, incorporating EVs with their unique protein and miRNAs signature into the list of promising new biomarkers is a logical next step. In this review, we discuss the general characteristics and technical aspects of EVs isolation and characterization. We discuss results of recent in vitro, in vivo, and patients study describing the role of EVs in different inflammatory diseases and traumatic organ injuries. miRNAs and protein signature of EVs found in patients with acute organ injury are also debated.

摘要

由于全球范围内发病率和死亡率持续居高不下,因此需要开发新的策略,以便快速、准确、有价值地识别创伤和多发伤患者的现有损伤模式。已经证明细胞外囊泡 (EVs) 有助于促进临近细胞以及健康和患病机体中远处细胞之间的细胞间通讯过程。EVs 转移的 miRNA 和蛋白质在维持生理条件下正常器官结构和功能方面发挥着生物学作用。在病理条件下,EVs 改变 miRNA 和蛋白质货物的组成,从而介导或抑制损伤后果。因此,将具有独特蛋白质和 miRNA 特征的 EVs 纳入有前途的新型生物标志物列表是合乎逻辑的下一步。在这篇综述中,我们讨论了 EVs 分离和表征的一般特征和技术方面。我们讨论了最近的体外、体内和患者研究的结果,这些研究描述了 EVs 在不同炎症性疾病和创伤性器官损伤中的作用。还讨论了在急性器官损伤患者中发现的 EVs 的 miRNA 和蛋白质特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c98/9192467/16e49af29c85/68_2021_1607_Fig1_HTML.jpg

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