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Neutrophil - derived microparticles can induce pathological changes of acute respiratory distress syndrome in rats |
Wang Xiang-meng, Xiao Wen-kai, Deng Lie-hua |
Intensive Care Unit, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China |
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Abstract Objective: To investigate the effect of neutrophil-derived microparticles on the histopathological features of lung tissue in rats. 〖WTHZ〗Methods〓〖WTBZ〗Neutrophils were extracted from the peripheral venous blood of rats and NDMPs were extracted from the neutrophils stimulated with LPS. The NDMPs were qualitatively and quantitatively analyzed by the nanoparticle tracking analyzer. The rats were divided into 3 groups: control group, LPS group and NDMPs group. The rats in control group, LPS group and NDMPs group were given 100 μL saline, LPS (5 mg/kg) and NDMPs (2.0×109/kg) respectively by endobronchial injection. The changes of lung histological changes were observed by HE staining, lung wet/dry weight ratio, MPO activity in lung tissue and expression of various inflammatory factors in bronchoalveolar lavage fluid after 24 hours. 〖WTHZ〗Results〓〖WTBZ〗Compared with the control group, HE staining of LPS group and NDMPs group showed a large number of inflammatory infiltration, alveolar and interstitial hemorrhage, edema and other pathological changes; LPS group and NDMPs group lung injury score and lung wet and dry ratio was higher than the control (P<0.05). Lung injury score of NDMPs group was lower than that of LPS group (P<0.01), lung wet and dry ratio of NDMPs group was lower than that of LPS group (P<0.05), MPO activity of lung tissue and cytokines in bronchoalveolar lavage fluid of NDMPs group and LPS group were higher than those of control group (P<0.01). The expression of IL-1β in bronchoalveolar lavage fluid of LPS group was higher than that of the control group (P<0.01). The expression of IL-1β in bronchoalveolar lavage fluid in NDMPs group was higher than that in control group (P<0.05). In NDMPs group, the expression of inflammatory cytokines TNF-α, IL-1β and IL-10 expression were lower than LPS group (P<0.05). 〖WTHZ〗Conclusion〓〖WTBZ〗LPS-induced neutrophil-derived microparticles can cause pathological changes of acute respiratory distress syndrome in rats.
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Received: 02 August 2017
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Corresponding Authors:
Deng Lie-hua, E-mail:glinson@126.com
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[1]Bernard GR, Artigas A, Brigham KL. The American-European Consensus Conference on ARDS. Definitions, mechanisms, relevant outcomes, and clinical trial coordination[J]. Am J Respir Crit Care Med, 1994, 149(3 Pt 1): 818-824.
[2]Villar J, Fernández RL, Ambrós A, et al. A clinical classification of the acute respiratory distress syndrome for predicting outcome and guiding medical therapy[J]. Crit Care Med, 2015, 43(2): 346-353.
[3]Dalli J, Montero-Melendez T, Norling LV, et al. Heterogeneity in neutrophil microparticles reveals distinct proteome and functional properties[J]. Mol Cell Proteomics, 2013, 12(8): 2205-2219.
[4]Angelillo-Scherrer A. Leukocyte-derived microparticles in vascular homeostasis[J]. Circ Res, 2012, 110(2): 356-369.
[5]Pluskota E, Woody NM, Szpak D, et al. Expression, activation, and function of integrin alphaMbeta2 (Mac-1) on neutrophil-derived microparticles[J]. Blood, 2008, 112(6): 2327-2335.
[6]Pitanga TN, de Arago Frana L, Rocha VC, et al.Neutrophil-derived microparticles induce myeloperoxidase-mediated damage of vascular endothelial cells[J]. BMC Cell Biol, 2014, 15:21.
[7]Johnson BL Ⅲ, Kuethe JW, Caldwell CC. Neutrophil derived microvesicles:emerging role of a key mediator to the immune response[J]. Endocr Metab Immune Disord Drug Targets, 2014, 14(3):210-217.
[8]高林,丁凤华,王向蒙,等. 血浆中性粒细胞来源微颗粒与ARDS患者氧合指数和机械通气的关系[J]. 中国急救医学, 2016, 36(10):900-903.
[9]Ko SF, Hsu SY, Chen CH, et al. Human lung cancer-derived microparticles enhanced angiogenesis and growth of hepatoma cells in rodent lung parenchyma[J]. Am J Transl Res, 2016, 8(3): 1302-1318.
[10]Smith KM, Mrozek JD, Simonton SC, et al. Prolonged partial liquid ventilation using conventional and high-frequency ventilatory techniques: gas exchange and lung pathology in an animal model of respiratory distress syndrome[J]. Crit Care Med, 1997, 25(11):1888-1897.
[11]Wu D, Pan P, Qin Q. Research progress of pathogenesis of acute lung injury/acute respiratory distress syndrome[J]. Zhonghua Jie He He Hu Xi Za Zhi, 2015, 38(7):524-527.
[12]Johnson BL 3rd, Midura EF, Prakash PS, et al. Neutrophil derived microparticles increase mortality and the counter-inflammatory response in a murine model of sepsis[J]. Biochim Biophys Acta, 2017, 1863(10 Pt B):2554-2563.
[13]Li H, Meng X, Gao Y, et al. Isolation and phenotypic characteristics of microparticles in acute respiratory distress syndrome[J]. Int J Clin Exp Pathol, 2015, 8(2):1640-1648.
[14]Guervilly C, Lacroix R, Forel JM, et al. High levels of circulating leukocyte microparticles are associated with better outcome in acute respiratory distress syndrome[J]. Crit Care, 2011, 15(1):R31.
[15]Bhatia M, Moochhala S. Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome[J]. J Pathol, 2004, 202(2): 145-156.
[16]Walter JM, Wilson J, Ware LB. Biomarkers in acute respiratory distress syndrome: from pathobiology to improving patient care[J]. Expert Rev Respir Med, 2014, 8(5):573-586.
[17]Armstrong L, Milla AB. Relative production of tumor necrosis factor alpha and interleukin 10 in adult respiratory distress syndrome[J]. Thorax, 1997, 52(5): 442-446.
[18]Ma CH, Liu JP, Qu R, et al. Tectorigenin inhibits the inflammation of LPS-induced acute lung injury in mice[J]. Chin J Nat Med, 2014, 12(11):841-846.
[19]王婷, 梁华平, 柴鉴深,等. 三种大鼠急性肺损伤模型的比较[J]. 成都医学院学报, 2016, 11(1):5-9 |
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