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人视网膜色素上皮细胞与T淋巴细胞的激活 被引量:1

Human retinal pigment epithelial cells and T-lymphocyte activation
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摘要 目的 观察人视网膜色素上皮(RPE)细胞人类白细胞抗原(HLA)-DP、-DQ、DR抗原和CD40抗原的表达,以确定它们在免疫应答过程中的分子表达和刺激T淋巴细胞活化的能力。方法人RPE细胞分别在γ-干扰素诱导和无诱导的条件下培养,免疫组织化学染色方法测定HLA—DP、-DQ、-DR抗原和CD40抗原在RPE细胞中的表达。体外共同培养人RPE细胞和外周血单个核细胞,荧光活化细胞分类仪测定其中活化的T淋巴细胞CD69的表达。结果γ-干扰素能够诱导HLA—DP、DQ、-DR抗原表达升高和CD40在人RPE细胞上的表达,CD69阳性的T淋巴细胞,在人RPE细胞与外周血单个核细胞的共同培养系统中的含量增加。结论人RPE细胞能够激活外周血中T淋巴细胞,是一种具有免疫学特性潜能的抗原递呈细胞。 Objective To investigate the expression of Human leucocyte antigen(HLA)-DP, -DQ, DR and CD40 in human retinal pigment epithelial (RPE) cells, to determine their molecule expression in immune response process, and their abilities to stimulate T lymphocyte activation. Methods Human RPE cells were cultured with or without ( IFN respectively. Expression of HLA DP, -DQ, -DR and CD40 was measured by immunohistoehemical staining. Meanwhile, peripheral blood mononuclear cells (PBMC) were co-cultured with RPE cells in vitro, and then the expression of activated lymphocytes CD69 was measured by fluorescence activated cell sorter(FACS). Results Expression of HLA-DP, -DQ, -DR and CD40 antigen were enhanced by Y-interferon inducement. Increasing amount of CD69 positive lymphocytes were found in the co-culture system of RPE cells and PBMC. Conclusion T-lymphoeytes in the peripheral blood were activated by human RPE cells which is antigen presenting cells with immunological characteristics potential.
作者 王帆
出处 《中华眼底病杂志》 CAS CSCD 北大核心 2008年第5期355-358,共4页 Chinese Journal of Ocular Fundus Diseases
关键词 色素上皮 HLA—D抗原/生理学 T淋巴细胞/免疫学 细胞培养技术 免疫组 织化学 Pigment epithelium of eye HLA-D antigens/ physiology T-Lymphocytes/ immunology Cell culture techniques Immunohistochemistry
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  • 1Larkin DF, Alexander RA, Cree IA. Infiltrating inflammatory cell phenotypes and apoptosis in rejected human corneal allografts. Eye, 1997, 11: 68-74.
  • 2Larkin DF, Calder VL, Lightman SL. Identification and characterization of cells infiltrating the graft and aqueous humour in rat corneal allograft rejection. Clin Exp Immunol, 1997, 107: 381-391.
  • 3Durie FH, Foy TM, Masters SR, et al. The role ot CD40 in the regulation of humoral and cell mediated immunity. Immunol Today, 1994, 15: 406-411.
  • 4Bertelmann E, Jaroszewski J, Pleyer U. Corneal allograft rejection: current understanding. 2: clinical implications, Ophthalmologica, 2002, 216: 2-12.
  • 5Engelmann K, Friedl P. Optimization of culture conditions for human corneal endothelial cells. In Vitro Cell Dev Biol, 1989, 25: 1065-1072.
  • 6Plskova J, Kuffova L, Holan V, et al. Evaluation of corneal graft rejection in a mouse model. Br J Ophthalmol, 2002, 86: 108-113.
  • 7Iwata M, Soya K, Sawa M, et al. CD40 expression in normal human cornea and regulation of CD40 in cultured human corneal epithelial and stromal cells. Invest Ophthalmol Vis Sci, 2002, 43: 348-357.
  • 8Celia M, Scheidegger D, Palmer-Lehmann K, et al. Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation. J Exp Med, 1996, 184: 747- 752.
  • 9Salomon B, Bluestone JA. Complexities of CD28/B7:CTLA-4 costimulatory pathways in autoimmunity and transplantation. Annu Rev Immunol, 2001, 19: 225-252.
  • 10Yang Y, Wilson JM. CD40 ligand-dependent T cell activation: requirement of BT-CD28 signaling through CD40. Science, 1996, 273: 1862-1864.

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