Fujikawa L S, Reay C, Morin M E
Ocular Immunology Laboratory, Smith-Kettlewell Eye Research Foundation, Pacific Presbyterian Medical Center, San Francisco, California 94115.
Invest Ophthalmol Vis Sci. 1989 Jan;30(1):66-73.
Class II histocompatibility complex antigens on the retinal vascular endothelium may allow these cells to function as antigen-presenting cells to circulating T cells. The present study investigated induction of class II antigens in vitro to characterize the response under controlled conditions. Retinal vascular endothelium from Lewis and Brown Norway rats (high versus low responders in experimental autoimmune uveitis) were exposed in vitro to recombinant rat gamma interferon, interleukin-1, interleukin-2, or Concanavalin-A spleen supernatant. Retinal pericytes, macrophages and lymphocytes were studied in comparison. A newly adapted ELISA technique was used to assay levels of antigen expression. Class II antigens (I-A OX6, I-E OX17, polymorphic I-A OX3), class I antigens (OX18), macrophage marker (OX42), macrophage and T helper cell marker (W3/25), and T suppressor/cytotoxic cell marker (OX8) were studied. Results showed that retinal vascular endothelium normally expresses very little class II antigen. However, high levels of I-A and I-E were induced by interferon or spleen supernatant. The levels of class II antigen approached that of the traditional antigen-presenting cell (macrophage) and were much higher than levels for pericytes and lymphocytes. The same doses of interferon showed larger increases in the Lewis rat compared to Brown Norway. No effect was seen with interleukin-1 or -2. Therefore, retinal vascular endothelium may be induced by gamma interferon to express class II antigens with degree of induction greater than or equal to the macrophage, and higher levels of induction were seen in the high responder strain.(ABSTRACT TRUNCATED AT 250 WORDS)
视网膜血管内皮细胞上的II类组织相容性复合体抗原可能使这些细胞作为抗原呈递细胞作用于循环中的T细胞。本研究在体外研究II类抗原的诱导情况,以在可控条件下表征该反应。将Lewis大鼠和棕色挪威大鼠(实验性自身免疫性葡萄膜炎中的高反应者与低反应者)的视网膜血管内皮细胞在体外暴露于重组大鼠γ干扰素、白细胞介素-1、白细胞介素-2或伴刀豆球蛋白A脾上清液。作为对照,对视网膜周细胞、巨噬细胞和淋巴细胞进行了研究。采用一种新改良的酶联免疫吸附测定(ELISA)技术来检测抗原表达水平。研究了II类抗原(I-A OX6、I-E OX17、多态性I-A OX3)、I类抗原(OX18)、巨噬细胞标志物(OX42)、巨噬细胞和T辅助细胞标志物(W3/25)以及T抑制/细胞毒性细胞标志物(OX8)。结果显示,视网膜血管内皮细胞通常表达极少的II类抗原。然而,干扰素或脾上清液可诱导I-A和I-E高水平表达。II类抗原水平接近传统抗原呈递细胞(巨噬细胞)的水平,且远高于周细胞和淋巴细胞的水平。相同剂量的干扰素在Lewis大鼠中引起的增加幅度大于棕色挪威大鼠。白细胞介素-1或-2未产生影响。因此,γ干扰素可诱导视网膜血管内皮细胞表达II类抗原,诱导程度大于或等于巨噬细胞,且在高反应者品系中诱导水平更高。(摘要截短于250词)