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CXC类趋化因子12及其受体在口腔扁平苔藓中的表达 被引量:3

The study on the expression of CXCL12 and CXCR4 in OLP
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摘要 目的:检测CXCL12及CXCR4在口腔扁平苔藓中(OLP)的表达及分布。方法:将31例OLP黏膜标本按病损类型分型、分级,免疫组化检测CXCL12及CXCR4的表达,测量CXCL12及CXCR4的累积光密度值(IOD)。结果:1OLP组织中可以检测到CXCL12及CXCR4表达,其表达向表层扩展且逐渐增强。2依临床分型分组,网纹组、糜烂组与对照组差异均具有统计学意义(P<0.05);网纹型与糜烂型相比,CXCL12的IOD降低,CXCR4的IOD升高,网纹组与糜烂组差异无统计学意义(P>0.05)。3CXCL12及CXCR4依临床分级分组,5组之间的差异没有统计学意义(P>0.05),且临床分级与IOD无明显相关性(P>0.05)。4CXCL12的IOD与CXCR4的IOD呈正相关。结论:CXCL12及CXCR4在OLP中分布及表达的差异,提示CXCL12/CXCR4轴在OLP的发生发展中可能起到一定作用。 Objective:To explore the expression of CXCL12 and CXCR4 in normal oral mucosa and OLP of different clinical classifications at the level of protein. Method:OLP specimens(experimental group) were grouped respectively according to clinical classification and the score of clinical manifestation. The expressions of CXCL12 and CXCR4 were observed in different tissues using IH. Result:1According to the clinical classifications,the expressions of CXCL12 and CXCR4 in general group and erosive group were both higher compared to the normal oral mucosa,differences were considered statistically significant(P〈0.05).The dyeing sites of CXCL12 and CXCR4 in general group were similar to that of erosive group,but the staining intensity of CXCL12 was weaker while that of CXCR4 was stronger. The difference of the expression between general group and erosive group was not statistically significant(P〉0.05). 2Both CXCL12 and CXCR4 had no statistically significant differences among five groups based on the clinical manifestation(P〉0.05) and the IOD of both CXCL12 and CXCR4 had no obvious correlation with the clinical manifestation(P〉0.05).3The staining intensity of CXCL12 had positive correlation with that of CXCR4. Conclusion:The enhancement and distribution of CXCL12 and CXCR4 expression in OLP suggested CXCL12/CXCR4 may be involved in OLP development and progression.
出处 《临床口腔医学杂志》 2015年第2期67-70,共4页 Journal of Clinical Stomatology
基金 国家自然科学基金面上项目(21350005131205)
关键词 口腔扁平苔藓 CXCL12 CXCR4 免疫组化 OLP CXC12 CXCR4 IH
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参考文献21

  • 1陈谦明.口腔黏膜病学[M].第3版.北京:人民卫生出版社,2009:201-202.
  • 2Cencioni Cv Capogrossi MC,Napolitano M. The SDF-I / CXCR4 axis in stem cell preconditioning DJ. Cardiovasc Res, 2012, 94 (3) : 400- 407.
  • 3杨志峰,杨清玲,陈昌杰.趋化因子SDF-1与受体CXCR4的研究进展[J].分子诊断与治疗杂志,2011,3(1):58-61. 被引量:35
  • 4Bagan -SebastianJV, Milian -Masanet MA, Penarrocha -Diago M, et al. A clinical study of 205 patients with oral lichen planus DJ.J Oral Maxillofac Surg, 1992,50(2): 116-118.
  • 5Thongprasom K, Luangjarmekom L, Sererat T, et al. Relative efficacy of fluocinolone acetonide compared with triamcinolone acetonide in treatment of oral lichen planus DJ.J Oral Pathol Med, 1992, 21 C1 0) : 456-458.
  • 6Crump MP, GongJH, Loetscher P, et al. Solution structure and basis for functional activity of stromal cell-derived factor-I; dissociation of CXCR4 activation from binding and inhibition of HIV-I DJ. EM?BOJ, 1997,16(23) :6996-7007.
  • 7Gozansky EK,LouisJM,Caffrey M,et al. Mapping the binding of the N -terminal extracellular tail of the CXCR4 receptor to stromal cell?derived factor-lalphaDJ.J Mol Biol' 2005, 345 (4): 651-658.
  • 8Hatse S, BalzariniJ, Liekens S. Stromal cell-derived factor I CCX?CL12) binds to endothelial cells and signals through a receptor dif?ferent from CXCR4 DJ. Biochem Biophys Res Commun. 2006, 348 (1): 192-199.
  • 9Karin N. The multiple faces of CXCL12 (SDF-Ialpha) in the regu?lation of immunity during health and disease DJ.J Leukoc Biol. 2010,88(3):463-473.
  • 10Kitaori Lito Hv Schwarz EM,et al. Stromal cell-derived factor 1/ CXCR4 signaling is critical for the recruitment of mesenchymal stem cells to the fracture site during skeletal repair in a mouse model[J] . Arthritis Rheum, 2009, 60(3): 813-823.

二级参考文献31

  • 1方慧云,王秦秦.肺癌与细胞因子[J].国外医学(肿瘤学分册),2005,32(8):605-608. 被引量:3
  • 2Scully C, Eisen D, Carrozzo M. Management of oral lichen planus[J]. Am J Clin Dennatol, 2000(1):287-306.
  • 3Scully C, Carrozzo M. Oral mucosal disease: Lichen planus [J]. Br J Oral Maxinof Surg, 2008(46) : 15-21.
  • 4Jungell P, Konuinen Y T, Nortamo P, et al. Immunoelectron microscopic study of distribution of T cell subsets in oral lichen planus[J]. Scand J Dent Res, 1989(97):361-367.
  • 5Pinsky M R. Dysregulation of the immune response in severe sepsis[J]. Am J ned Sei, 2004, 328(4) :220-229.
  • 6Gorehk L, Flavell R A. Mechanism of transfenning growth factor beta-induced inhibition of T helper type 1 differentiation [J]. J Exp M, 2002, 19(5) : 14-99.
  • 7Kojawski L A, Talpaz M. The role of Interferon-alpha in the treatment of chronic myeloid leukemia [ J ]. Cytokine Growth Factor Rev, 2007, 18(5/6) :459-471.
  • 8Balabanian K, Lagane B, Infantino S, et al. The ehemokine SDF-1/CXCL12 binds to and signals through the orphan receptor RDC1 in T lymphocytes[J]. J Biol Chem, 2005, 280(42): 35760-35766.
  • 9Wong D, Korz W. Translating an Antagonist of Chemokine Receptor CXCR4: From Bench to Bedside[J]. Clin Cancer Res, 2008; 14(24): 7975-7980.
  • 10Busillo J M, Benovic J L. Regulation of CXCR4 Signaling[J]. Biochim Biophys Acta, 2007, 1768(4): 952- 963.

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