Zheng B B, Zhang Y, Sun N N, Huang W H, Meng Y
Department of Respiratory and Critical Care Medicine, Chronic Airway Disease Laboratory, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zhonghua Yi Xue Za Zhi. 2018 Jun 12;98(22):1780-1785. doi: 10.3760/cma.j.issn.0376-2491.2018.22.011.
To explore the effect and mechanism of exosome derived from lipopolysaccharide (LPS)-induced mouse macrophage (RAW264.7) on acute lung injury. RAW264.7 were cultured and divided into 2 groups: control group and LPS-induced group. The exosomes were extracted from the two groups of cell supernatant by ultracentrifugation and classified into 2 groups: C-EXO group and LPS-EXO group. random allocation was used to averagely divide the eighteen male C57BL/6 mice into 3 groups: control group, EXO-control group and EXO-LPS group. All mice were sacrificed after 12 h. The lung tissue was used for HE staining to assess the degree of acute lung injury as well as immunohistochemical staining for interleukin (IL) -1β and tumor necrosis factor (TNF)-α. The tissue protein expression levels of IL-1β, TNF-α, β-catenin, E-cadhein, ZO-1 and Occludin were measured by Western blot. alveolar type Ⅱ epithelial cells (MLE-12) were cultured and divided into 3 groups: C-control group, EXO-control-induced group and EXO-LPS-induced group. The tissue protein expression levels of IL-1β, TNF-α, and Occludin were measured by Western blot after 12 h. The two samples of C-EXO group and LPS-EXO group was proved to be exosomes. Under a light microscope, the lung tissue of EXO-LPS group showed inflammatory cell infiltration, hemorrhage, interstitial and alveolar edema, and the thickness of alveolar septum. The tissue protein levels of IL-1β and TNF-α in EXO-LPS group were obviously higher than the control group, EXO-control group (1.331±0.203 and 0.274±0.018, 0.892±0.074; 0.800±0.096 and 0.596±0.025, 0.441±0.061; all <0.05). While the tissue protein levels of Occludin showed the opposite phenomenon (0.251±0.021 and 0.862±0.029, 0.453±0.013; all <0.05). Compared with the C-control group and the EXO-control-induced group, the expression levels of IL-1β and TNF-α increased significantly in the EXO-LPS-induced group (0.900±0.033 and 0.320±0.030, 0.661±0.028; 0.739±0.045 and 0.151±0.024, 0.360±0.037; all <0.05). whereas the protein levels of Occludin expression were reversed in MLE-12 (0.585±0.082 and 0.941±0.090, 0.732±0.083; all <0.05). Exosomes derived from LPS-induced RAW264.7 can induced the acute lung injury by affecting barrier function, which probably is related to the low degree of Occludin in alveolar type Ⅱ epithelial cells.
探讨脂多糖(LPS)诱导的小鼠巨噬细胞(RAW264.7)来源的外泌体对急性肺损伤的影响及机制。培养RAW264.7细胞并分为2组:对照组和LPS诱导组。通过超速离心从两组细胞上清液中提取外泌体,并分为2组:C-EXO组和LPS-EXO组。采用随机分组法将18只雄性C57BL/6小鼠平均分为3组:对照组、EXO-对照组和EXO-LPS组。12小时后处死所有小鼠。取肺组织进行HE染色以评估急性肺损伤程度,并进行白细胞介素(IL)-1β和肿瘤坏死因子(TNF)-α的免疫组化染色。通过蛋白质免疫印迹法检测IL-1β、TNF-α、β-连环蛋白、E-钙黏蛋白、紧密连接蛋白1(ZO-1)和闭合蛋白的组织蛋白表达水平。培养肺泡Ⅱ型上皮细胞(MLE-12)并分为3组:C-对照组、EXO-对照诱导组和EXO-LPS诱导组。12小时后通过蛋白质免疫印迹法检测IL-1β、TNF-α和闭合蛋白的组织蛋白表达水平。证实C-EXO组和LPS-EXO组的两个样本均为外泌体。在光学显微镜下,EXO-LPS组的肺组织显示有炎性细胞浸润、出血、间质和肺泡水肿以及肺泡间隔增厚。EXO-LPS组的IL-1β和TNF-α组织蛋白水平明显高于对照组、EXO-对照组(1.331±0.203和0.274±0.018,0.892±0.074;0.800±0.096和0.596±0.025,0.441±0.061;均P<0.05)。而闭合蛋白的组织蛋白水平则呈现相反的现象(0.251±0.021和0.862±0.029,0.453±0.013;均P<0.05)。与C-对照组和EXO-对照诱导组相比,EXO-LPS诱导组的IL-1β和TNF-α表达水平显著升高(0.900±0.033和0.320±0.030,0.661±0.028;0.739±0.045和0.151±0.024,0.360±0.037;均P<0.05)。而在MLE-12细胞中闭合蛋白的蛋白水平则相反(0.585±0.082和0.941±0.090,0.732±0.083;均P<0.05)。LPS诱导的RAW264.7来源的外泌体可通过影响屏障功能诱导急性肺损伤,这可能与肺泡Ⅱ型上皮细胞中闭合蛋白水平降低有关。