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气泡诱导的内皮微粒促进内皮功能障碍。

Bubble-Induced Endothelial Microparticles Promote Endothelial Dysfunction.

作者信息

Yu Xuhua, Xu Jiajun, Huang Guoyang, Zhang Kun, Qing Long, Liu Wenwu, Xu Weigang

机构信息

Department of Diving and Hyperbaric Medicine, Faculty of Naval Medicine, the Second Military Medical University, Shanghai, China.

出版信息

PLoS One. 2017 Jan 23;12(1):e0168881. doi: 10.1371/journal.pone.0168881. eCollection 2017.

Abstract

Decompression sickness is a systemic pathophysiological process caused by bubbles and endothelial microparticles (EMPs) are established markers reflecting competency of endothelial function and vascular biology. Here, we investigated the effects of bubble-induced EMPs on endothelial cells in vitro and vivo. Rat pulmonary microvascular endothelial cells (PMVECs) were isolated and stimulated by bubbles and bubble-induced EMPs were collected and incubated with normal PMVECs in vitro. Cell viability and apoptosis were detected using Cell Counting Kit-8 assay and Annexin V FITC/PI double staining, respectively. Cell permeability and pro-inflammatory cytokines were determined by electric cell substrate impedance sensing and enzyme-linked immunosorbent assay, respectively. Intracellular nitric oxide and reactive oxygen species production were analyzed microscopically. In vivo study, bubble-induced EMPs were intravenously injected to the rats and soluble thrombomodulin, intercellular adhesion molecule 1, and vascullar adhesion molecule 1 were involved in evaluating endothelial dysfunction. In our study, bubble stimulus resulted in a significant increase of EMPs release by 3 fold. Bubble-induced EMPs significantly decreased cell viability and increased cell apoptosis. Moreover, bubble-induced EMPs induced abnormal increase of cell permeability and over-expression of pro-inflammatory cytokines. Intracellular ROS production increased while NO production decreased. These negative effects caused by bubble-induced EMPs were remarkably suppressed when EMPs pretreated with surfactant FSN-100. Finally, intravenous injection of bubble-induced EMPs caused elevations of soluble thrombomodulin and pro-inflammatory cytokines in the circulation. Altogether, our results demonstrated that bubble-induced EMPs can mediate endothelial dysfunction in vitro and vivo, which can be attenuated by EMPs abatement strategy. These data expanded our horizon of the detrimental effects of bubble-induced EMPs, which may be of great concern in DCS.

摘要

减压病是一种由气泡引起的全身性病理生理过程,而内皮微粒(EMPs)是反映内皮功能和血管生物学状态的既定标志物。在此,我们研究了气泡诱导的EMPs在体外和体内对内皮细胞的影响。分离大鼠肺微血管内皮细胞(PMVECs),用气泡刺激,收集气泡诱导的EMPs并在体外与正常PMVECs共同孵育。分别使用细胞计数试剂盒-8法和膜联蛋白V FITC/PI双染法检测细胞活力和凋亡情况。分别通过电细胞基质阻抗传感和酶联免疫吸附测定法测定细胞通透性和促炎细胞因子。通过显微镜分析细胞内一氧化氮和活性氧的产生。在体内研究中,将气泡诱导的EMPs静脉注射到大鼠体内,并通过可溶性血栓调节蛋白、细胞间黏附分子1和血管黏附分子1来评估内皮功能障碍。在我们的研究中,气泡刺激导致EMPs释放显著增加3倍。气泡诱导的EMPs显著降低细胞活力并增加细胞凋亡。此外,气泡诱导的EMPs导致细胞通透性异常增加和促炎细胞因子过度表达。细胞内活性氧产生增加而一氧化氮产生减少。当用表面活性剂FSN-100预处理EMPs时,由气泡诱导的EMPs引起的这些负面影响得到显著抑制。最后,静脉注射气泡诱导的EMPs导致循环中可溶性血栓调节蛋白和促炎细胞因子升高。总之,我们的结果表明,气泡诱导的EMPs可在体外和体内介导内皮功能障碍,而这种功能障碍可通过减少EMPs的策略得到减轻。这些数据拓宽了我们对气泡诱导的EMPs有害影响的认识,这在减压病中可能备受关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf01/5256891/2e03cc0ffd78/pone.0168881.g001.jpg

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