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IL-32及TNF-α在哮喘小鼠肺组织中的表达及布地奈德的干预作用 被引量:11

Expression of Interleukin-32 and Tumor Necrosis Factor Alpha and the effects of Budesonide in mice with asthma
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摘要 目的:探讨哮喘小鼠发病过程中白细胞介素32(IL-32)及肿瘤坏死因子-α(TNF-α)在肺内表达的变化及布地奈德的干预作用。方法:将30只健康雌性BALB/c小鼠随机分为3组:卵蛋白(OVA)致敏并激发的哮喘模型组(A组),OVA致敏、激发并予布地奈德吸入治疗组(B组)及正常对照组(C组),每组10只。观察卵蛋白激发及布地奈德干预后哮喘小鼠气道的病理变化;免疫组织化学染色观察IL-32及TNF-α表达的变化。结果:IL-32及TNF-α在对照组中呈低表达,在哮喘组中表达明显增加,使用布地奈德干预后,IL-32及TNF-α的表达明显降低(P<0.05),且二者表达量均与气道壁厚度呈正相关(r=0.716,P<0.05;r=0.459,P<0.05)。结论:IL-32及TNF-α可能参与了哮喘小鼠气道重塑过程,布地奈德干预改善哮喘小鼠的气道重塑可能与降低IL-32及TNF-α的表达有关。 Objective:To study the expression of Interleukin-32(IL-32) and Tumor Necrosis Factor Alpha(TNF-α) in the airway and the effect of Budesonide on their expression in mice with asthma.Methods:Thirty BALB/c Female mices were randomly divided into three groups: placebo control group,untreated asthma group,and Budesonide-treated asthma group.The asthma group were induced by intraperitoneal injection of 10% ovalbumin(OVA) on days 1,8 and 15,and then from days 22 to 34,challenged by inhalation of 2% OVA aerosol every other day.The Budesonide-treated asthma group received an inhalation of Budesonide(1 mg) before OVA challenge.The pathological changes of the airway were assessed by hematoxylin and eosin staining.The immunohistochemistry was used to estimate the expression of IL-32 and TNF-αin the lung.Results:The expression of IL-32 and TNF-αin the lung was low in the control group and increased significantly in the untreated asthma group(P0.05),but decreased significantly in the Budesonide-treated asthma group..Both IL-32(r=0.716,P0.05) and TNF-α(r=0.459,P0.05) were positively correlated with the thickness of the airway wall.Conclusion:IL-32 and TNF-α may be associated with airway remodeling inmice with asthma.Budesonide can improve airway remodeling,possibly by decreasing the expression of IL-32 and TNF-α.
出处 《中国妇幼保健》 CAS 北大核心 2012年第5期743-746,共4页 Maternal and Child Health Care of China
关键词 哮喘 气道重塑 IL-32 TNF-Α 小鼠 Asthma Airway remodeling Interleukin-32 TNF-α Mice
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参考文献14

  • 1Shoda H, Fujio K, Yamaguchi Yet al. Interactions between IL - 32 and tumor necrosis factor alpha contribute to the exacerbation of immune - inflammatory diseases [ J ] . Arthritis Res Ther, 2006, 8 ( 6 ) : 166.
  • 2Joosten LA, Netea MG, Kim SH et al. IL -32, a proinflammatory cytokine in rheumatoid arthritis [J].Proe Natl Acad Sci USA, 2006, 103 (9) : 3298.
  • 3Cagnard N, Letourneur F, Essabbani A et al. Interleukin - 32, CCL2, PF4F1 and GFDIO are the only cytokine/chemokine genes differentially expressed by in vitro cultured rheumatoid and osteoarthritis fibroblast - like synoviocytes [J] . Eur Cytokine Netw, 2005, 16 (4) : 289.
  • 4Shioya M, Nishida A, Yagi Yet al. Epithelial overexpression of interleukin - 32 - alpha in inflammatory bowel disease [ J] . Clin Exp Immunol, 2007, 149 (3): 480.
  • 5Kim KH, Shim JH, Seo EH et al. Interleukin - 32 monoclonal antibodies for immunohistochemistry, Western blotting, and ELISA [J]. J Immunol Methods, 2008, 333 (1-2): 38.
  • 6Du Q, Chen Z, Zhou LF et al. Inhibitory effects of astragaloside IV on ovalbumin-induced chronic experimental asthma [J] . Can J Physiol Pharmacol, 2008, 86 (7) : 449.
  • 7Rydell Trmanen K, Uller L, Erjefalt JS. Remodeling of extra - bronchial lung vasculature following allergic airway inflammation [ J ] . Respir Res, 2008, 9:18.
  • 8Coda C, Kanaji T, Kanaji Set al. Involvement of IL -32 in activation induceded cell death in T ceils[J] . International Immunology, 2006, 18 (2): 233.
  • 9Obase Y, Shimoda T, Milsula K et al. Correlaction between airway hyperresponsiveness and airway inflammation in a young adult population: eosinophil, ECP, and cytokine levels in induced sputum [J].. Ann Allergy Asthma Immunol, 2001, 86 (3) : 304.
  • 10Susumu Nakae, Carolina Lunderius. TNF can contribute to muhiple features of ovalbumin - induced allergic inflammation of the airways in mice [J]. J Allergy Clin Immunol, 2007, 119 (3) : 680.

同被引文献90

  • 1杨红霞,张建勇,陈玲.白细胞介素32对哮喘小鼠气道黏蛋白5ac分泌的影响作用[J].中国实用内科杂志,2013,33(S1):88-88. 被引量:1
  • 2李梅.老年慢性支气管哮喘患者血清TNF-α、IL-6水平及其临床意义[J].放射免疫学杂志,2005,18(6):440-441. 被引量:18
  • 3王豪,沈霞,沈铮.血清ECP和EOS数与支气管哮喘的关系[J].交通医学,1997,11(1):1-2. 被引量:1
  • 4Dinarello CA, Kim SH. IL- 32, a novel cytokine with a possible role in disease[J]. Ann Rheum Dis, 2006, 65(Suppl 3) : iii61- iii64.
  • 5Kim SH, Han SY, Azam T, et al. Interleukin -32: a cytokine and inducer of TNFalpha[J]. Immunity, 2005, 22( 1 ) : 131 - 142.
  • 6Nishida A, Andoh A, Inatomi O, et al. Interleukin - 32 expression in the pancreas[J]. J Biol Chem,2009, 284(26): 17868 - 17876.
  • 7Joosten LA, Netea MG, Kim SH, et al. IL- 32, a proinflammatory cytokine in rheumatoid arthritis [ J]. Proc Natl Acad Sci USA,2006,103(9):3298—3303.
  • 8Kobayashi H, Lin PC. Molecular characterization of IL - 32 in hu- man endothelial cells[ J. Cytokine, 2009, 46(3) : 351 - 358.
  • 9Shioya M, Nishida A, Yagi Y, et al. Epithelial overexpression of interleukin- 32α in inflammatory bowel disease [ J]. Clin Exp Im- munol, 2007, 149(3) : 480-486.
  • 10Netea MG, Azam T, Ferwerda G, et al. IL - 32 synergizes with nu- cleotide oligomerization domain ( NOD ) 1 and NOD2 ligands for IL - 1 beta and IL - 6 production through a caspase 1 - dependent mechanism [ J]. Proc Natl Acad Sci USA, 2005, 102 (45) : 16309 - 16314.

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