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肿瘤坏死因子-α在中耳胆脂瘤的表达及其对邻近骨质的作用 被引量:3

A study on expression of tumor necrosis factor alpha in middle ear cholesteatoma and its effect on bone destruction
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摘要 目的 :探讨肿瘤坏死因子 - α(TNF- α)在中耳胆脂瘤中的表达及其对邻近骨质的作用。方法 :应用TNF- α单克隆抗体对 18例中耳胆脂瘤组织和 8例正常外耳道、面部皮肤和鼓膜进行免疫定位检测。结果 :TNF-α定位于胆脂瘤组织的上皮及上皮下结缔组织 ,较正常外耳道及鼓膜的染色明显增强。结论 :TNF- α在中耳胆脂瘤组织中有较高表达并通过两条途径引起骨质吸收 :1TNF- α作为自分泌调节因子引起破骨性骨吸收 ;2 TNF-α作为中间信使 ,激活炎性细胞释放一系列生物酶引起骨组织脱钙 ,骨基质、骨蛋白溶解 ,最终导致骨质吸收。 Objective:To determine the expression and localization of tumor necrosis factor alpha(TNF α) in human middle ear cholesteatoma and its effects on bone resorption.Method:The distribution of TNF α in 18 cholesteatoma tissues and 8 normal external ear canal skin, facial skin and tympanic memebrane were studied immunohistochemically with paraffin embedded sections.Result:TNF α was localized in the epitheliun and connective tissue of cholesteatomas studied, particularly on basal and spinous cells and macrophages.The epithelium of normal external ear canal skin , facial skin and tympanic membrane was slightly stained.Conclusion:This study revealed significantly increased level of TNF α in cholesteatoma tissues.TNF α acts both directly,by causing bone erosion as an autocrine growth factor,and indirectly as an important mediator by stimulating the release of enzymes causing bone destruction.
出处 《临床耳鼻咽喉科杂志》 CSCD 北大核心 2001年第2期66-67,I002,共3页 Journal of Clinical Otorhinolaryngology
关键词 中耳胆脂瘤 肿瘤坏死因子-A 骨质吸收 Middle ear cholesteatoma Tumor necrosis factor alpha Bone destruction
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参考文献2

  • 1Yan S D,Am J Otolaryngol,1991年,12卷,83页
  • 2Yan S D,Ann Otol Rhinol Laryngol,1991年,100卷,157页

同被引文献25

  • 1张武宁,唐安洲,徐志文,谭颂华.慢性化脓性中耳炎的咽鼓管功能对手术疗效的影响[J].中华耳科学杂志,2004,2(2):114-118. 被引量:10
  • 2孙文忠,徐志文,唐安洲,苏纪平.PTKs CDK4及p15在中耳胆脂瘤上皮的表达[J].临床耳鼻咽喉科杂志,2004,18(10):616-619. 被引量:7
  • 3王辉兵,徐志文,唐安洲,苏纪平.中耳胆脂瘤基质金属蛋白酶2,9的活性检测及临床意义[J].临床耳鼻咽喉科杂志,2004,18(10):620-622. 被引量:14
  • 4张鄂,龚树生.缺氧诱导因子-1α及诱导型一氧化氮合酶在中耳胆脂瘤上皮中的表达及意义[J].临床耳鼻咽喉头颈外科杂志,2007,21(10):463-465. 被引量:2
  • 5Park HJ, Park K. Expression of Fas/APO-1 and apoptosis of keratinocytesin human cholesteatoma. Laryngoscope, 1999, 109(4):613-616.
  • 6Park K, Chun YM, Lee DH. Expression of phospholipase C-γ1 in experimental cholesteatoma using Mongolian gerbils. Acta Otolaryngol,2001; 121(4): 477-480.
  • 7Shibosawa E, Tsutsumi K, Takakuwa T, et al. Stromal expression of matrix metalloprotease-9 in middle ear cholesteatomas. Am J Otol,2000,21(5): 621-624.
  • 8Akimoto R, Pawankar R, Yagi T, et al. Acquired and congenital cholesteatoma: determination of tumor necrosis factor-alpha, intercellular adhesion molecule-1, interleukin-1-alpha and lymphocyte functional antigen-1 in the inflammatory process. ORL Otorhinolaryngol Relat Spec, 2000, 62(5): 257-265.
  • 9Schmidt M., Grunsfelder P, Hoppe F. Up-regulation of matrix metalloprotease-9 in middle ear cholesteatoma-correlations with growth factor expression in vivo? Eur Arch Otolaryngol, 2001,258 (9): 472-476.
  • 10Sudhoff H, Dazert S, Gonzales A, et al. Angiogenesis and angiogenic growth factors in middle ear cholesteatoma. Am J Otol, 2000, 21 (6):793-798.

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