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首页> 外文期刊>Investigative ophthalmology & visual science >Expression of indoleamine 2,3-dioxygenase in human corneal cells as a local immunosuppressive factor.
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Expression of indoleamine 2,3-dioxygenase in human corneal cells as a local immunosuppressive factor.

机译:吲哚胺2,3-二加氧酶在人角膜细胞中的表达作为局部免疫抑制因子。

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摘要

PURPOSE: To identify the localization of indoleamine 2,3-dioxygenase (IDO) in human corneal cells and to evaluate its functional ability as a local immunosuppressive factor. METHODS: The expression profile of IDO was identified in primary cultures of human corneal cells (fibroblasts, epithelial cells, endothelial cells) by RT-PCR and Western blot analysis. The immunosuppressive function of IDO was assessed by culturing human CD4(+) T cells with conditioned medium derived from the three types of human corneal cells, and changes in proliferation and apoptosis were determined. IDO expression and its apoptotic effects on CD4(+) T cells were also investigated after IFN-gamma treatment. RESULTS: Among the three types of human corneal cells, IDO mRNA and protein expression were observed in human corneal fibroblasts and epithelial cells, with higher levels in the human corneal fibroblasts. Human CD4(+) T cells cultivated in conditioned medium derived from human corneal fibroblasts showed decreased cell proliferation and increased apoptosis. IFN-gamma treatment significantly induced IDO expression and showed apoptotic effects on immune cells. CONCLUSIONS: These results suggest that human corneal fibroblasts are relatively immunoresistant and that the IDO expression can act as one of the factors for the maintenance of immune privilege in the cornea.
机译:目的:鉴定吲哚胺2,3-二加氧酶(IDO)在人角膜细胞中的定位,并评估其作为局部免疫抑制因子的功能。方法:通过RT-PCR和Western blot分析鉴定IDO在人角膜细胞(成纤维细胞,上皮细胞,内皮细胞)原代培养物中的表达。 IDO的免疫抑制功能是通过使用衍生自三种人角膜细胞的条件培养基培养人CD4(+)T细胞来评估的,并确定了增殖和凋亡的变化。 IFN-γ处理后,还研究了IDO表达及其对CD4(+)T细胞的凋亡作用。结果:在三种类型的人角膜细胞中,在人角膜成纤维细胞和上皮细胞中观察到IDO mRNA和蛋白质表达,在人角膜成纤维细胞中表达较高。在源自人角膜成纤维细胞的条件培养基中培养的人CD4(+)T细胞显示出细胞增殖减少和凋亡增加。 IFN-γ处理显着诱导IDO表达,并显示对免疫细胞的凋亡作用。结论:这些结果表明,人角膜成纤维细胞具有相对的免疫抵抗性,IDO的表达可以作为维持角膜免疫特权的因素之一。

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