人内皮细胞免疫表型分析。

Y Kubota, T J Lawley
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摘要

我们对人内皮细胞的免疫学特性了解甚少。在这项研究中,我们对培养的人皮肤微血管内皮细胞与人脐静脉内皮细胞进行了免疫表型分析,并检测了各种生物反应修饰剂改变表型的能力。通过FACS分析,两种类型的细胞似乎都缺乏免疫精通细胞的许多细胞表面标记物,例如OKT4, OKT8, Leu7, FcIgG受体,补体受体,IL-2受体和HLA-Dr,但它们具有β 2微球蛋白和DAF。HLA-Dr抗原可以通过γ - ifn在两种类型的内皮细胞上以剂量和时间依赖的方式诱导。两种类型的内皮细胞都具有多种细胞粘附分子(Cell Adhesion Molecules, CAMs),如ICAM-1、CD44、LFA-3,但不具有LFA-1和CD2。两种内皮细胞暴露于γ - ifn、IL-1和TNF均可上调ICAM-1,但不上调LFA-3或CD44。这些数据表明,真皮微血管内皮细胞可能在多种不同的皮肤炎症中发挥核心作用。
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[Immunophenotypic analysis of human endothelial cells].

Very Little is known about the immunological attributes of human endothelial cells. In this study, we performed immunologic phenotypic analysis of cultured human dermal microvascular endothelial cells in comparison with human umbilical vein endothelial cells and examined the ability of various biologic response modifiers to alter the phenotypes. Using FACS analysis, both types of the cells appear to lack many of the cell surface markers of immunologically proficient cells, E.G. OKT4, OKT8, Leu7, FcIgG receptor, complement receptors, IL-2 receptor and HLA-Dr, but they possess beta 2-microglobulin and DAF. HLA-Dr antigens can be induced on both types of endothelial cells by gamma-IFN in a dose and time dependent manner. Both types of endothelial cells possess several kinds of Cell Adhesion Molecules (CAMs), such as ICAM-1, CD44, LFA-3, but not LFA-1 or CD2. ICAM-1 but not LFA-3 or CD44 can be upregulated by exposure of both types of endothelial cells to gamma-IFN, IL-1 and TNF. These data suggest that endothelial cells of the dermal microvasculature may play central roles in a variety of different cutaneous inflammation.

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