全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
-  2017 

高迁移率族蛋白B1和Toll样受体4与哮喘气道炎症的关系及维生素D的作用
Relationship of HMGB1 and TLR4 with airway inflammation in asthma and the role of vitamin D

DOI: 10.7652/jdyxb201704012

Keywords: 高迁移率族蛋白B1(HMGB1),Toll样受体4(TLR4),哮喘,气道炎症,1,25-(OH)2D3,Th1/Th2
high mobility group box 1 (HMGB1)
,TLR4,asthma,airway inflammation,1,25-(OH)2D3,Th1/Th2

Full-Text   Cite this paper   Add to My Lib

Abstract:

摘要:目的 探讨高迁移率族蛋白B1(HMGB1)和Toll样受体4(TLR4)与气道炎症的关系及维生素D的作用。方法 BALB/c小鼠随机分为对照组、哮喘组和1,25-(OH)2D3干预组(每组8只)。采用HE染色观察小鼠肺组织病理学变化并应用计算机图像系统测定支气管壁厚度,采用免疫组化法观察肺组织HMGB1和TLR4表达,同时收集支气管肺泡灌洗液(BALF)和外周血,将BALF进行细胞学检测,用酶联免疫吸附法(ELISA)测定BALF和外周血中HMGB1、TLR-4、白介素-4(IL-4)和干扰素-γ(IFN-γ)含量。结果 哮喘组小鼠肺组织HMGB1和TLR4表达较强,干预组表达较弱。哮喘组BALF中白细胞总数及嗜酸性粒细胞、中性粒细胞和淋巴细胞比例明显升高,单核/巨噬细胞比例明显下降(均为P<0.05);干预组BALF中白细胞总数及嗜酸性粒细胞、中性粒细胞和淋巴细胞比例明显下降,单核/巨噬细胞比例明显上升(均为P<0.05)。哮喘组BALF和外周血中HMGB1、TLR4和IL-4含量均明显高于对照组,IFN-γ含量均明显低于对照组(均为P<0.05);干预组BALF和外周血中HMGB1、TLR4和IL-4含量均明显低于哮喘组,IFN-γ含量明显高于哮喘组(均为P<0.05)。BALF中HMGB1和TLR4含量分别与细胞总数和IL-4浓度均呈正相关(r1为0.796、0.730;r2为0.695、0.648;均为P<0.05)。结论 HMGB1和TLR4与气道炎症和免疫紊乱有关;适量1,25-(OH)2D3可减轻气道炎症,可能与调节Th1/Th2细胞平衡有关。
ABSTRACT: Objective To evaluate the relationship of high mobility group box 1 (HMGB1) and TLR4 with airway inflammation and the role of vitamin D. Methods Totally 24 BALB/c mice were randomly divided into control group, asthma group, and 1,25-(OH)??2D??3 group, each having 8 mice. The pathological changes in lung tissue of the mice were observed by hematoxylin-eosin (HE) staining, bronchial wall thickness was measured with computer pathological image analysis system software. The expressions of HMGB1 and TLR4 in lung tissue were detected by immunohistochemical method. Bronchoalveolar lavage fluid (BALF) was collected for cytological examination; the contents of HMGB1, TLR4, IL-4 and IFN-γ in BALF and the peripheral blood were detected by enzyme-linked immunosorbent assay (ELISA). Results The expressions of HMGB1 and TLR4 in lung tissue were stronger in asthma group, but weaker in intervention group. The total number of leukocytes as well as the percentages of eosinophils, neutrophils and lymphocytes increased significantly in BALF in asthma group, but significantly decreased in intervention group (all P<0.05). The ratio of monocyte/macrophage significantly decreased in asthma group, but increased significantly in intervention group (P<0.05). The contents of HMGB1, TLR4 and IL-4 in BALF and the peripheral blood were significantly higher in asthma group than in control and intervention groups, whereas IFN-γ level was significantly lower than that in control and intervention groups (all P<0.05). HMGB1 and TLR4 contents had a positive correlation with the total number of cells and IL-4 concentration in BALF, respectively (r1=0.796, 0.730; r2=0.695, 0.648; all P<0.05). Conclusion HMGB1 and TLR4 were associated with airway inflammation and immune disorders. An appropriate amount of 1,25-(OH)2D3 can relieve airway inflammation, which may be

References

[1]  BARKAUSKAITE V, EK M, POPOVIC K, et al. Translocation of the novel cytokine HMGB1 to the cytoplasm and extracellular space coincides with the peak of clinical activity in experimentally UV-induced lesions of cutaneous lupus erythematosus[J]. Lupus, 2007, 16(10):794-802.
[2]  HANSDOTTIR S,MONICK MM.Vitamin D effects on lung immunity and respiratory diseases[J].Vitam Horm, 2011, 86:217-237.
[3]  TEMELKOVSKI J, HOGAN SP, SHEPHERD DP, et al. An improved murine model of asthma: selective airway inflammation, epithelial lesions and increased methacholine responsiveness following chronic exposure to aerosolised allergen[J]. Thorax, 1998, 53(10):849-856.
[4]  HUANG TJ, MACARY PA, EYNOTT P, et al. Allergen-specific Th1 cells counteract efferent Th2 cell-dependent bronchial hyperresponsiveness and eosinophilic inflammation partly via IFN-γ[J]. J Immunol, 2001, 166(1):207-226.
[5]  BAEKE F, KORF H, OVERBERGH L, et al. The vitamin D analog, TX527, promotes a human CD4+CD25highCDl2710w regulatory T cell profile and induces a migratory signature specific for homing to sites of inflammation[J]. J Immunol, 2011, 186(1):132-142.
[6]  DOGRU M, KIRMIZIBEKMEZ H, YESILTEPE MUTLU RG, et al. Clinical effects of vitamin D in children with asthma[J]. Int Arch Allergy Immunol, 2014, 164(4):319-325.
[7]  MATHEU V, B?FCK O, MONDOC E, et al. Dual effects of vitamin D-induced alteration of TH1/TH2 cytokine expression: enhancing IgE production and decreasing airway eosinophilia in murine allergic airway disease[J]. J Allergy Clin Immunol, 2003, 112(3):585-592.
[8]  李如霞,侯进飞,周瑾思,等. 1,25-二羟基维生素D3对尘螨引起的P815肥大细胞TLR4表达和IL-4分泌影响的初步研究[J]. 中华微生物学和免疫学杂志, 2015, 35(3):188-193.
[9]  王学亮,周传麟,王丽娜. 维生素D对支气管哮喘患者Th1/Th2平衡的调节作用及IL-17的影响[J]. 国际呼吸杂志, 2015, 35(1):9-11.
[10]  SADEGHI K, WESSNER B, LAGGNER U, et al. Vitamin D3 down-regulates monocyte TLR expression and triggers hyporesponsiveness to pathogen-associated molecular patterns[J]. Eur J Immunol, 2006, 36(2):361-370.
[11]  ENTEZARI M, WEISS DJ, SITAPARA R, et al. Inhibition of high-mobility group box1 protein (HMGBl) enhances bacterial clearance and protects against Pseudomonas Aeruginosa pneumonia in cystic fibrosis[J]. Mol Med, 2012, 18(3):477-485.
[12]  GOLDSTEIN RS, BRUCHFELD A, YANG L, et al. Cholinergic anti-inflammatory pathway activity and high mobility group box-1 (HMGB1) serum levels in patients with rheumatoid arthritis[J]. Mol Med, 2007, 13(3-4):210-215.
[13]  齐?b禄,杨敬平,银雪,等. 外周血中 TLR4、TIRAP 表达与脓毒症相关性研究[J]. 临床肺科杂志, 2015, 20(1):19-22.
[14]  MAYUZUMI H, OHKI Y, TOKUYAMA K, et al. Age-related difference in the persistency of allergic airway inflammation and bronchial hyperresponsiveness in a murine model of asthma[J]. Int Arch Allergy Immunol, 2007, 143(4):255-262.
[15]  VENKAYYA R, LAM M, WILLKOM M, et al. The Th2 lymphocyte products IL-4 and IL-13 rapidly induce airway hyper-responsiveness through direct effects on resident airway cells[J]. Am J Respir Cell Mol Biol, 2002, 26(2):202-208.
[16]  HAMADA N, MAEYAMA T, KAWAGUCHI T, et al. The role of high mobility group box1 in pulmonary fibrosis[J]. Am J Respir Cell Mol Biol, 2008, 39(4):440-447.
[17]  付亮,蔡绍曦,赵海金,等. N-乙酰半胱氨酸对哮喘小鼠肺组织HMGB1、RAGE表达的影响[J]. 南方医科大学学报, 2008, 28(5):692-695.
[18]  LEE CC, LAI YT, CHANG HT, et al. Inhibition of high-mobility group box1 in lung reduced airway inflammation and remodeling in a mouse model of chronic asthma[J]. Biochem Pharmacol, 2013, 86(7):940-949.
[19]  谭小玉,侯长春,陈俊健,等. IL-1β诱导支气管上皮细胞高迁移率族蛋白1主动释放[J].重庆医学, 2015, 44(2):151-154.
[20]  刘勇,黄亮,杨继斌,等. 不同潮气量机械通气对复苏犬支气管灌洗液中TOLL样受体4变化的影响[J]. 中国急救医学, 2012, 32(8):704-708.
[21]  STRAUB C, MIDORO-HORIUTI T, GOLDBLUM R. Elucidating the role of high mobility group box1 (HMGB1) cytokine in a murine model of allergic asthma[J]. J Allergy Clin Immu, 2010, 125(2):AB108.
[22]  YANG Q, LIU X, YAO Z, et al. Penehyclidine hydrochloride inhibits the release of high-mobility group box 1 in lipopolysaccharide-activated RAW264.7 cells and cecal ligation and puncture-induced septic mice[J]. J Surg Res, 2014, 186(1):310-317.
[23]  MUSUMECI D, ROVIELLO GN, MONTESARCHIO D. An overview on HMGB1 inhibitors as potential therapeutic agents in HMGB1-related pathologies[J]. Pharmacol Ther, 2014, 141(3):347-357.
[24]  SUNDEN-CULLBERG J, NORRBY-TEGLUND A, ROUHIAINEN A, et al. Persistent elevation of high mobility group box-1 protein (HMGB1) in patients with severe sepsis and septic shock[J]. Crit Care Med, 2005, 33(3):564-573.
[25]  WU J, KOBAYASHI M, SOUSA EA, et al. Differential proteomic analysis of bronchoalveolar lavage fluid in asthmatics following segmental antigen challenge[J]. Mol Cell Proteomics, 2005, 4(9):1251-1264.
[26]  贾晨虹,王建,董力,等. 糖皮质激素对哮喘患者外周血单核细胞 TLR4和相关炎症因子表达的影响[J]. 实用临床医药杂志, 2015, 19(23):41-43.
[27]  CHEN WJ, HOU XJ, YANG SF, et al. Effect of vitamin D supplementation during pregnancy on the Th1/Th2 cell balance of rat offspring[J]. Pharmazie, 2014, 69(5):385-390.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133