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结节性红斑患者皮损处CD68和VEGF的表达

Expression of CD68 and VEGF in Skin Lesion of Erythema Nodosum Patients
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摘要 目的 研究结节性红斑皮损中CD68和VEGF的表达情况,探讨上述因素在其发病中的作用机理。方法采用Max Vision TM免疫组织化学染色法检测49例结节性红斑患者皮损(疾病组)及10例正常皮肤组织(对照组)CD68和VEGF分子的表达情况。结果 疾病组CD68阳性表达率为95.92%,显著高于正常组CD68阳性表达率(60.00%),差异有统计学意义(P<0.01);疾病组VEGF阳性表达率为95.92%,显著高于正常组VEGF阳性表达率(60.00%),差异有统计学意义(P<0.01)。结论 CD68和VEGF在EN皮损处的高表达,提示EN皮损处有大量处于激活状态的炎细胞浸润、聚集,引起血管内皮细胞损伤,考虑炎症反应和内皮细胞损伤参与了结节性红斑皮损的发病。 Objective To Study the CD68 and VEGF expression in skin lesion tissue and their functions in pathogenesis of the erythema nodosum.Methods The expression of CD68 and VEGF in the skin lesions of 49 cases of erythema nodosum patients(disease group)and 10 cases of normal human(control group)were detected by MaxVision TM immunohistochemical staining method.Results Compared with the normal contol group(60.00%),the positive expression rate of CD68 in disease group(95.92%)was increased significantly,with statistical differences between two grouqs(P<0.01).Compared with the normal control group(60.00%),the positive egression rate of VEGF in disease group(95.92%)was increased significantly with statistical dififerences between two groups(P<0.01).Conclusion Higher expression of CD68 and VEGF in skin lesions was concluded that active inflammatory cells and injury of endothelial cell were participated in pathogenesis of erythema nodosum.
作者 张佳丽 韩晨珠 丁晨 王以可 李保强 ZHANG Jia-li;Han Chen-zhu;DING Cheng;WANG Yi-ke;LI Bao-qiang(Department of Dermatology and venereology,The Affiliated Hospital of Chengde Medical University,Chengde,Hebei,067000,China;Luohe Second People's Hospital)
出处 《承德医学院学报》 2023年第2期108-111,共4页 Journal of Chengde Medical University
关键词 结节性红斑 免疫组化 CD68 VEGF erythema nodosum immunohistochemical CD68 VEGF
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  • 1王红,杨培增,彭晓燕,周红颜,黄祥坤,刘云霞.共刺激分子在Behcet病患者结节红斑组织中的表达[J].首都医科大学学报,2005,26(3):258-262. 被引量:4
  • 2Topaloglu R, Sungur A, Baskin E, et al. Vascular endothelial growth factor in Henoch - Schonlein purpura. J Rheumatol 2001 ; 28: 2269 -2273.
  • 3Brown LF, Harrist TJ, Yeo KT, et al. Increased expression of vascular permeability factor (vascular endothelial growth factor) in bullous pemphigoid, dermatitis herpetifonnis, and erythema multiforme. J Invest Dermatol. 1995;104:744- 749.
  • 4Lee DH, Cho HJ, Kim JT, et al. Expression of vascular endothelial growth factor and inducible nitric oxide synthase in pterygia. Cornea 2001 ;20:738 - 742.
  • 5Viac J, Palacio S, Schmitt D, et al. Expression of vascular endothelial growth factor in normal epidermis, epithelial tumors and cultured keratinocytes. Arch Dermatol Res 1997;289:158 - 163.
  • 6Shimizu Y, Sakai M, Umemura Y, et al. Immunohistochemical localization of nitric oxide synthase in normal human skin: expression of endothelial - type and inducible - type nitric oxide synthase in kerafinoeytes. J Dermatol. 1997;24:80- 87.
  • 7Gross SS, Wolin MS. Nitric oxide: pathophysiological mechanism.Annu Rev Phyciol 1995;57:737 - 769.
  • 8Yokoyama K, Mitomi H, Kobayashi K, et al. Obliterative arteritis with nitric oxide synthase and HLA - DR expression in Crohn' s colitis. Hepatogastroenterology 2001 ;48:401 - 407.
  • 9Jozkowicz A, Cooke JP, Guevara I, et al. Genetic augmentation of nitric oxide synthase increases the vascular generation of VEGF. Cardiovasc Res 2001 ;51:773 - 834.
  • 10Lal BK, Varma S, Pappas PJ, et al. VEGF increases permeability of the endothelial cell monolayer by activation of PKB/akt, endothelial nitric - oxide synthase, and MAP kinase pathways. Microvasc Res 2001 ;62:252 - 262.

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