Platts K E, Benson M T, Rennie I G, Sharrard R M, Rees R C
Institute for Cancer Studies, University of Sheffield, United Kingdom.
Invest Ophthalmol Vis Sci. 1995 Oct;36(11):2262-9.
The purpose of this study was to assess qualitatively the expression of adhesion molecules by human retinal pigment epithelium (RPE) and to study their regulation by inflammatory cytokines. These molecular events and the role played by inflammatory cytokines are important for selective lymphocyte trafficking into the eye during uveitis.
Expression of intracellular adhesion molecule-1 (ICAM-1), endothelial leukocyte adhesion molecule-1 (ELAM-1), platelet endothelial cell adhesion molecule-1 (PECAM-1), and vascular adhesion molecule (VCAM-1) by early passage human RPE cells was assessed by flow cytometry. In addition, the regulation of the expression of these molecules by the inflammatory cytokines interleukin-1 beta (IL-1 beta), IL-6, tumor necrosis factor alpha (TNF alpha), and interferon gamma (IFN gamma) was determined. Reverse transcription-polymerase chain reaction (RT-PCR) was used to characterize further adhesion molecule expression.
Flow cytometric analysis determined that ICAM-1 was constitutively expressed on RPE cell lines and that in the presence of TNF alpha, IFN gamma, and IL-1 beta, there was a median fold increase in expression of 4.4, 5.4, and 4.4, respectively. In contrast, flow cytometric analysis of ELAM-1, PECAM-1, and VCAM-1 indicated that these adhesion molecules were not constitutively expressed at the cell surface; only the expression of VCAM-1 was upregulated by the presence of cytokines. The results of RT-PCR on RPE cells indicated that mRNA for all the adhesion molecules was present constitutively in some RPE cultures. After activation with IFN gamma, TNF alpha, and IL-1 beta, RT-PCR analysis showed that the number of RPE cell lines expressing all the adhesion molecules increased.
ICAM-1 expression is markedly upregulated by inflammatory cytokines. Although mRNA for other adhesion molecules is expressed in RPE cells and is enhanced by inflammatory cytokines, this does not necessarily reflect the cell surface protein expression. Thus, the expression of adhesion molecules by RPE cells, and the subsequent recruitment of specific leukocytes, may be determined by the local cytokine environment.
本研究旨在定性评估人视网膜色素上皮(RPE)中黏附分子的表达,并研究炎症细胞因子对其的调节作用。这些分子事件以及炎症细胞因子所起的作用对于葡萄膜炎期间淋巴细胞选择性向眼内迁移至关重要。
通过流式细胞术评估早期传代的人RPE细胞中细胞间黏附分子-1(ICAM-1)、内皮白细胞黏附分子-1(ELAM-1)、血小板内皮细胞黏附分子-1(PECAM-1)和血管黏附分子(VCAM-1)的表达。此外,还测定了炎症细胞因子白细胞介素-1β(IL-1β)、IL-6、肿瘤坏死因子α(TNFα)和干扰素γ(IFNγ)对这些分子表达的调节作用。采用逆转录聚合酶链反应(RT-PCR)进一步表征黏附分子的表达。
流式细胞术分析确定ICAM-1在RPE细胞系中组成性表达,并且在TNFα、IFNγ和IL-1β存在的情况下,表达的中位数分别增加了4.4倍、5.4倍和4.4倍。相比之下,对ELAM-1、PECAM-1和VCAM-1的流式细胞术分析表明,这些黏附分子在细胞表面并非组成性表达;只有VCAM-1的表达因细胞因子的存在而上调。对RPE细胞进行RT-PCR的结果表明,所有黏附分子的mRNA在某些RPE培养物中组成性存在。在用IFNγ、TNFα和IL-1β激活后,RT-PCR分析显示表达所有黏附分子的RPE细胞系数量增加。
炎症细胞因子可显著上调ICAM-1的表达。虽然其他黏附分子的mRNA在RPE细胞中表达并被炎症细胞因子增强,但这不一定反映细胞表面蛋白的表达。因此,RPE细胞中黏附分子的表达以及随后特定白细胞的募集可能由局部细胞因子环境决定。