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儿童表皮兜甲蛋白及内披蛋白的表达与特应性皮炎的发病机制探讨 被引量:5

The expression of epidermal terminal differentiation protein of children with atopic dermatitis
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摘要 目的探讨特应性皮炎(atopic dermatitis,AD)儿童急性病损期皮肤2种终末分化蛋白的表达情况,从皮肤屏障功能障碍方面研究AD的发病机制。方法选取中、重度AD患儿作为AD组,通过皮肤环钻术获取皮肤标本,以正常皮肤为对照,对兜甲蛋白(loricrin,LOR)及内披蛋白(involucrin,INV)2种表皮终末分化蛋白进行免疫组化研究。结果发现在AD患儿急性病损期皮肤,2种分化蛋白染色强度较正常对照组均减弱,应用图像分析系统对2种分化蛋白染色结果进行分析显示,与对照组相比,平均光密度、积分光密度明显降低(P<0.05),阳性面积百分比差异无统计学意义(P>0.05)。结论 2种终末分化蛋白表达异常导致的皮肤屏障功能障碍可能是AD发病原因之一。 Ojective To st udy the expression ofth ree ter minal differentiation protein in acute lesions ofatopic der matitis(A D)child ren i n order to explore the mechan ism ofA D. Methods P u nch biopsies were collected from acute lesions ofA D(moderate or severe)child ren and nor mal healthy skin. T he expression offilagg r i n(FLG),involucr in(I N V) and lor icr in(LOR)were investigated by im munohistochemistry. Results The staining intensit y oft h ree protei n decrea sed i n acute lesional sk i n ofA D subject s wa s fou nd. Mea n opt ical den sit y(m OD, i nteg r al optical density(i OD)sig nificantly decreased in involved A D skin as compared to skin with nor mal subjects(P〈0.05). Conclusion The abnor mal expression oft h ree ter m i nal different iat ion proteini nduced skin barrier dysfu nct ion, which may play an impor tant role in the pathogenesis ofA D.
出处 《空军医学杂志》 2015年第1期26-28,共3页 Medical Journal of Air Force
基金 雅漾基金资助项目(CDA-2011-2-02)
关键词 特应性皮炎 免疫组化 皮肤屏障 终末分化蛋白 儿童 Atopic dermatitis Immunohistochemistry Skin barrier Terminal differentiation protein Children
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参考文献12

  • 1Leung DY,Bieber T.Atopic dermatitis[J].Lancet,2003,361(9352):151–160.
  • 2Chamlin SL,Frieden IJ,Williams ML,et al.Effects of atopic dermatitis on young American children and their families[J].Pediatrics,2004,114(3):607-611.
  • 3Suga r ma n J L,Flu h r J W,Fowler A J,et al.T he object ive severity assessment of atopic dermatitis score:an objective measu re usi ng per meabilit y bar r ier f u nction and st rat u m corneum hydration withcomputer-assisted estimates for extent of disease[J].Arch Dermatol,2003,139(11):1417-1422.
  • 4吕宏升,朱庆生,王军,朱锦宇,赵广跃,张大伟.全自动显微镜及图像分析系统处理免疫组化图像[J].中国体视学与图像分析,2004,9(1):37-40. 被引量:63
  • 5Nemes Z,Steinert PM.Bricks and mortar of the epidermal barrier[J].Exp Mol Med,1999,31(1):5-19.
  • 6Marekov LN,Steinert PM.Ceramides are bound to structural protenvelope[J].J Biol Chem,1998,273(28):17763-17770.
  • 7Koch PJ,de Viragh PA,Scharer E,et al.Lessons from loricrin deficient mice:compensatory mechanisms maintaining skin barrier function in the absence of a major cornified envelope protein[J].J Cell Biol,2000,151(2):389-400.
  • 8Hudson TJ.Skin bar rier f unction and allergic risk[J].Nat Genet,2006,38(4):399-400.
  • 9Spergel J M,Mizog uchi E,Brewer J P,et al.Epicutaneous sensitization with protein antigen induces localized allergic dermatitis and hyperresponsiveness to methacholine after single exposure to aerosolized antigen in mice[J].J Clin Invest,1998,101(8):1614-1622.
  • 10Jensen JM,Flster-Holst R,Baranowsky A,et al.Impaired sphingomyelinase activity and epider mal differentiation in atopic dermatitis[J].J Invest Dermatol,2005,122(6):1423-1431.

二级参考文献6

共引文献62

同被引文献65

  • 1王元.系统性红斑狼疮实验室检查研究进展[J].实用儿科临床杂志,2005,20(5):390-392. 被引量:5
  • 2Mlitz V, Latreille J, Gardinier S, et al. Impact of filaggrin muta- tions on Roman spectra and biophysical properties of the stratum corneum in mild to moderate atopic dermatitis [ J ]. J Eur Acad Dermatol Venereol, 2012, 26(8) : 983 - 990.
  • 3Kezic S, O'Regan GM, Yan N, et al. Levels of filaggrin degrada- tion products are influenced by both filaggrin genotype and atopic dermatitis severity[J]. Allergy, 2011, 66(7) :934 - 940.
  • 4Morar N, Edster P, Street T, et al. Fine mapping of susceptibili- ty genes for atopic dermatitis in the epidermal differentiation com- plex on chromosome lq21 [J ]. Br J Dermatol, 2007, 157 : 3.
  • 5Rosanne A HMvan den Oord. Filaggrin gene defects and risk of developing allergic sensitisation and allergic disorders: systematic review andmeta- analysis[J]. British Medical Journal, 2009, 339: 24 - 33.
  • 6Paternoster L, Standl M, Chen CM, et al. Meta - analysis of genome - vide association studies identifies three new risk loci for atopic; dermatitis[J]. Nat Genet, 2011, 44:87 - 192.
  • 7Mrabet - Dahbi S, Dalpke AH, Renz H. The Toll - like receptor 2 R753Q mutation modifies cytokine production and Toll - like re- ceptor expression in atopic dermatitis[J ]. J Allergy Clin Immunol, 2008, 121:1 013- 1 019.
  • 8Smith FJD, Irvine AD, Terron Kwiatkowski A, et al. Loss - of - function mutations in the gene encoding filaggrin cause ichthyosis vulgaris[J]. Nat Genet, 2006, 38 : 337 - 342.
  • 9Palmer CN, Irvine AD, Terron - Kwiatkowski A, et al. Common loss- of - function variants of the epidermal barrier protein filag- grin are a major predisposing factor for atopic dermatitis[J]. Nat Genet2006, 38:441 - 446.
  • 10谭雪晶.一氧化氮诱导正常人皮肤炎症反应的实验研究[J].中国皮肤性病学杂志,2008,22(4):193-197. 被引量:2

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