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IL-22在支气管哮喘患者血清中的表达及其受体IL-22R1在人气道细胞中的表达 被引量:4

Serum IL-22 level in asthmatic patients and expression of IL-22R1 in human airway cells
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摘要 目的检测IL-22在支气管哮喘患者血清中的表达,检测IL-22R1在人气道上皮细胞、气道平滑肌细胞、肺成纤维细胞中的表达,寻找IL-22作用的靶细胞。方法应用ELISA法检测36例支气管哮喘患者及20例正常对照者血清IL-22及IL-17的表达,同时检测36例患者肺通气功能,根据1秒率(FEV1/FVC)及FEV1占预计值的百分比将支气管哮喘患者分为支气管激发试验阳性组(17例)和支气管舒张试验阳性组(19例)。应用实时定量PCR检测人气道平滑肌细胞、人肺成纤维细胞、人气道上皮细胞IL-22R1 mRNA的表达,用免疫荧光以及蛋白质印迹法检测IL-22R1蛋白在上述3种细胞中的表达。结果支气管哮喘患者血清IL-22及IL-17水平与正常对照组相比差异无统计学意义,但支气管舒张试验阳性组患者血清IL-22和IL-17水平高于支气管激发试验阳性组(P<0.05)。IL-22R1mRNA及蛋白在上述3种细胞均有表达。结论 IL-22可能涉及支气管哮喘的发生发展过程,气道平滑肌细胞、肺成纤维细胞、人气道上皮细胞可能均是IL-22发挥作用的靶细胞。 Objective To examine the serum level of IL-22 in asthmatic patients and the expression of IL-22R1 in human airway epithelial cells,human airway smooth muscle cells,and lung fibroblasts,so as to explore the target cells of IL-22.Methods The serum levels of IL-22 and IL-17 in 36 asthmatic patients and 20 normal control subjects were measured by enzyme-linked immunosorbent assay (ELISA).And lung function of the asthmatic patients was assessed by Gaeger spirometry.According to the values of FEV1/FVC and FEV1%,the patients were divided into two groups:bronchodilation test positive group (19 patients) and bronchial provocation test positive group (17 patients).The expression of IL-22R1 mRNA in human airway epithelial cells,human airway smooth muscle cells,and lung fibroblasts was examined using real-time PCR,and IL-22R1 protein expression was detected by immunofluorescence staining and Western blotting analysis.Results There was no significant difference in serum IL-22 and IL-17 levels between the asthmatic patients and normal controls.The serum IL-22 and IL-17 levels in asthmatic patients positive for bronchodilation test was significantly higher than those positive for bronchial provocation test(P〈0.05).IL-22R1 mRNA and protein were detected in all the 3 types of cells.Conclusion IL-22 may be involved in the pathogenesis of asthma,and human airway epithelial cells,human airway smooth muscle cells,and lung fibroblasts may all be the target cells of IL-22.
出处 《第二军医大学学报》 CAS CSCD 北大核心 2010年第12期1291-1295,共5页 Academic Journal of Second Military Medical University
关键词 IL-22 IL-22R1 气道上皮细胞 气道平滑肌细胞 肺成纤维细胞 IL-22; IL-22R1; airway epithelial cell; airway smooth muscle cell; lung fibroblasts;
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  • 1Zhu J,Yamane H,Paul W E. Differentiation of effector CD4 T cell populations ( * ) [J]. Annu Rev Immunol, 2010,28:445-489.
  • 2Barczyk A,Pierzchala W,Sozanska E. Interleukiw17 in sputum correlates with airway hyperresponsiveness to methacholine [J]. Respir Med, 2003,97 : 726-733.
  • 3Agache I, Ciobanu C, Agache C, Anghel M. Increased serum IL- l7 is an independent risk factor for severe asthma[J]. Respir Med,2010,104:1131 -1137.
  • 4Kotenko S V, Izotova L S, Mirochnitchenko O V, Esterova E, Dickensheets H, Donnelly R P, et al. Identification of the functional interleukin-22 (IL-22) receptor complex: the IL- 10R2 chain (IL-10R beta ) is a common chain of both the IL-10 and IL-22 (IL-10-related T cell-derived inducible factor, IL-TIF) receptor complexes[J]. J Biol Chem, 2001,276 : 2725 -2732.
  • 5Log sdon N J, Jones g C, Aliman J C, Izotova L, Schwartz B, Pestka S,et al. The IL-10R2 binding hot spot on IL-22 is located on the N-terminal helix and is dependent on N linked glycosylation[J]. J Mol Biol,2004,342:503- 514.
  • 6Whittington H A,Armstrong L,Uppington K M,Millar A B. Interleukin-22: a potential immunomodulatory molecule in the lung[J]. Am J Respir Cell Mol Biol,2004,31:220- 226.
  • 7Aujla S J, Kolls J K. IL 22: a critical mediator in mucosal host defense[J]. J Mol Med,2009,87:451- 454.
  • 8支气管哮喘防治指南(支气管哮喘的定义、诊断、治疗和管理方案)[J].中华结核和呼吸杂志,2008,31(3):177-185. 被引量:2517
  • 9Watanabe S, Yamasaki A, Hashimoto K, Shigeoka Y, Chikumi H, Hasegawa Y, et al. Expression of functional leukotriene B4 receptors on human airway smooth muscle cells[J]. J Allergy Clin Immunol, 2009,124 : 59-65, e1-e3.
  • 10Ikeuchi H,Kuroiwa T, Hiramatsu N,Kaneko Y, Hiromura K Ueki K, et al. Expression of interleukin-22 in rheumatoid arthritis: potential role as a proinflammatory cytokine[J]. Arthritis Rheum,2005,52 : 1097-1046.

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  • 1宋颖芳,戚好文.支气管哮喘三种病理改变的分子生物学机制研究进展[J].国际呼吸杂志,2007,27(4):249-252. 被引量:1
  • 2Wolk K, Witte E, Witte K, et al, Biology of interleukin-22[J], Scmin Immunopathol, 2010, 32(1): 17-31.
  • 3Mirochnitchenko OV, Esterova E, Dickensheets H, et ai. Identification of the functional interleukin-22(IL-22)receptor complex: the IL-10R2 chain(IL-10rbeta)is a common chain of both the IL-10 and IL-22(IL-10-related T cell-derived inducible factor, IL-TIF)regeptor complexes[J]. J Biol Chem, 2001,276(4): 2725-32.
  • 4Logsdon NJ, Jones BC, Allman JC, et al. The IL-10R2 binding hot spot on IL-22 is located on the N.terminal helix and is dependent on N-linked glycosylation[J]. J Mol Biol, 2004, 342(2): 503-14.
  • 5Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-tirne quantitative PCR and the 2(-delta delta C(T))method [J], Methods, 2001,25(4): 402-8.
  • 6Chen J, Deng Y, Zhao J, et al. The polymorphism of IL-17 G-152a Was assoelated with childhood asthma and bacterial colonization of the hypopharynx in bronchiolitis[J]. J Clin Immunol, 2010, 30(4): 539-45.
  • 7Batra V, Musani AI, Hastie AT, et al. Bronchoalveolar lavage fluid concentrations of transforming growth factor(TGF)-beta1, TGF-beta2,interleukin(IL)-4 and IL-13 after segmental allergen challenge and their effects on alpha-smooth muscle actin and collagen Ⅲ synthesis by primary human lung f [J]. Clin Exp Allergy, 2004, 34(3):437-44.
  • 8Corry DB, Kheradmand F. Toward a comprehensive understanding of allergic lung disease [J]. Trans Am Clin Climatol Assoc, 2009, 120: 33-48.
  • 9Wolk K, Witte E, Wallaae E, et al. IL-22 regulates the expression of genes responsible for antimicrobial defense,cellular differentiation, and mobility in keratinocytes:a potential role it psoriaSls[J], Eur J Immunol, 2006, 36(5): 1309-23.
  • 10Kunz S, Wolk K, Witte E, et al. triterleukin(IL)-19,IL-20 and IL-24 are produced by and act on keratinocytes and are distinct from classical ILs[J]. Exp Dermatol, 2006, 15(12): 991-1004.

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