外泌体 miR-21-5p 的减少和 CD62p+ 外泌体的增加与多创伤患者败血症的发生有关。

IF 2.3 3区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS
Birte Weber , Dirk Henrich , Ingo Marzi , Liudmila Leppik
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引用次数: 0

摘要

败血症作为一种严重的全身性炎症,常常会导致器官功能障碍,进而导致死亡。在多发性创伤患者中,脓毒症并发症是导致晚期死亡的主要原因,占 45%,并给医疗系统带来极高的成本。因此,临床医生必须尽早发现败血症,以改善患者的预后。外泌体是诊断多发性创伤患者脓毒症并发症的一种很有前途的新诊断工具。研究人员在急诊室(ER)、创伤后24小时和5天收集了发生脓毒症(10人)和未发生脓毒症(10人)的多发性创伤患者(受伤严重程度评分(ISS)≥16)的血浆样本。通过基于微珠的多重流式细胞术测量表面表位,研究了EVs亚群,并与健康对照组(n = 10)的血浆EVs进行了比较。此外,外泌体细胞因子浓度是通过高灵敏度酶联免疫吸附法测定的,并与全身浓度相关。在 miRNA 货物分析方面,我们分析了 miRNA miR-1298-5p、miR-1262、miR-125b-5p、miR-92a-3p、miR-93-5p、miR-155-5p 和 miR-21-5p,并通过 RT-qPCR 比较了它们的外泌体浓度。脓毒性多创伤患者的 CD62p + 外泌体明显增加(p ≤ 0.05),而 CD40 + 外泌体和 CD49e + 外泌体则减少(p ≤ 0.05)。此外,我们还观察到,外泌体 IL-6 浓度反映了全身 IL-6 浓度(r2 = 0.63),在脓毒症患者和非脓毒症患者之间没有明显变化。所有患者和健康对照组的外泌体 IL-10 浓度似乎都是恒定的。我们观察到,外泌体中 miR-21-5p 的减少与脓毒症的发生有关(p ≤ 0.05),而脓毒症患者的外泌体 miR-93-5p、miR-155-5p 和 miR-92a-3p 没有特别的变化。综上所述,本研究在多创伤患者中进行的研究表明,败血症的发生与 CD62p + 外泌体的增加有关。此外,败血症患者的外泌体货物也发生了变化:miR-21-5p 减少了。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Decrease of exosomal miR-21-5p and the increase of CD62p+ exosomes are associated with the development of sepsis in polytraumatized patients

Sepsis as a severe systemic inflammation leads oftentimes to organ dysfunction and subsequently to death. In polytrauma patients, septic complications represent with 45% the predominant cause of late death and are responsible for extremely high costs in the healthcare system. Therefore, clinicians have to detect as early as possible the begin of sepsis to improve the patient's outcome. One new promising diagnostic tool to diagnose septic complications in polytraumatized patients are exosomes.

Plasma samples from polytraumatized patients (Injury Severity Score (ISS) ≥16) which developed sepsis (n = 10) and without sepsis (n = 10), were collected at emergency room (ER), 24h and 5 days after trauma. The EVs subpopulations were investigated by a bead-based multiplex flow cytometry measurement of surface epitopes and were compared with plasma EVs from healthy controls (n = 10). Moreover, exosomal cytokine concentrations were measured via high-sensitive ELISA and were correlated with systemic concentrations. For miRNA cargo analysis, we analysed the miRNAs miR-1298-5p, miR-1262, miR-125b-5p, miR-92a-3p, miR-93-5p, miR-155-5p and miR-21-5p and compared their exosomal concentrations by means of RT-qPCR.

CD62p + exosomes were significantly increased in septic polytrauma-patients (p ≤ 0.05), while CD40+exosomes, as well as CD49e + exosomes were diminished (p ≤ 0.05). Furthermore, we observed that the exosomal IL-6 concentration reflects the systemic IL-6 concentration (r2 = 0.63) and did not significantly alter between patients with and without sepsis. The exosomal IL-10 concentration seemed to be constant in all patients and healthy controls. We observed that a decrease of miR-21-5p in exosomes was associated with the development of sepsis (p ≤ 0.05), while exosomal miR-93-5p, miR-155-5p and miR-92a-3p were not specifically altered in septic patients.

Taken together, the present study in polytraumatized patients demonstrated that the development of sepsis is associated with an increase of CD62p + exosomes. Furthermore, the exosomal cargo was changed in septic patients: miR-21-5p was diminished.

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来源期刊
Molecular and Cellular Probes
Molecular and Cellular Probes 生物-生化研究方法
CiteScore
6.80
自引率
0.00%
发文量
52
审稿时长
16 days
期刊介绍: MCP - Advancing biology through–omics and bioinformatic technologies wants to capture outcomes from the current revolution in molecular technologies and sciences. The journal has broadened its scope and embraces any high quality research papers, reviews and opinions in areas including, but not limited to, molecular biology, cell biology, biochemistry, immunology, physiology, epidemiology, ecology, virology, microbiology, parasitology, genetics, evolutionary biology, genomics (including metagenomics), bioinformatics, proteomics, metabolomics, glycomics, and lipidomics. Submissions with a technology-driven focus on understanding normal biological or disease processes as well as conceptual advances and paradigm shifts are particularly encouraged. The Editors welcome fundamental or applied research areas; pre-submission enquiries about advanced draft manuscripts are welcomed. Top quality research and manuscripts will be fast-tracked.
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