Tomczok J, Sliwa-Tomczok W, Klein C L, Bittinger F, Kirkpatrick C J
Institute of Pathology, Johannes Gutenberg University Mainz, Germany.
Histochemistry. 1994 Nov;102(5):337-43. doi: 10.1007/BF00268904.
A semi-quantitative procedure is described, which allows the evaluation of expression levels of endothelial adhesion molecules on cultured human umbilical vein endothelial cells (HUVEC) using energy dispersive X-ray microanalysis (EDX). As a model two adhesion molecules, E-selection (CD62E; ELAM-1/endothelial leukocyte adhesion molecule-1) and ICAM-1 (intercellular adhesion molecule-1; CD54), were localized by the use of the silver-enhancement colloidal gold method after stimulation of HUVEC with endotoxin lipopolysaccharide (LPS), tumour necrosis factor (TNF) or a phorbol ester (PMA). The analysis was performed in a scanning electron microscope (SEM) at an accelerating voltage of 15 kV with scanned areas of 200 x 400 microns. The semi-quantitative data indicated that in LPS-treated groups both adhesion molecules were expressed at a significantly higher level than in all other groups (P < 0.01). In addition, after a 4 h treatment the expression levels of E-selectin in all groups were higher compared to ICAM-1. The experimental data from X-ray microanalysis were compared with data obtained from an enzyme-linked immunosorbent assay (ELISA) and similar values were found for both types of preparation. This microanalytical method is relatively simple and seems to be suitable for immunogold labelling studies on different types of endothelial cells in vitro.
本文描述了一种半定量方法,该方法可利用能量色散X射线微分析(EDX)评估培养的人脐静脉内皮细胞(HUVEC)上内皮粘附分子的表达水平。以两种粘附分子E选择素(CD62E;ELAM-1/内皮白细胞粘附分子-1)和细胞间粘附分子-1(ICAM-1;CD54)作为模型,在用内毒素脂多糖(LPS)、肿瘤坏死因子(TNF)或佛波酯(PMA)刺激HUVEC后,通过银增强胶体金法对其进行定位。分析在扫描电子显微镜(SEM)中进行,加速电压为15 kV,扫描区域为200×400微米。半定量数据表明,在LPS处理组中,两种粘附分子的表达水平均显著高于所有其他组(P<0.01)。此外,处理4小时后,所有组中E选择素的表达水平均高于ICAM-1。将X射线微分析的实验数据与酶联免疫吸附测定(ELISA)获得的数据进行比较,发现两种制剂的值相似。这种微分析方法相对简单,似乎适用于体外不同类型内皮细胞的免疫金标记研究。