Application of X-ray microanalysis to study of the expression of endothelial adhesion molecules on human umbilical vein endothelial cells in vitro.

Histochemistry Pub Date : 1994-11-01 DOI:10.1007/BF00268904
J Tomczok, W Sliwa-Tomczok, C L Klein, F Bittinger, C J Kirkpatrick
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引用次数: 2

Abstract

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.

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应用x射线显微分析研究体外人脐静脉内皮细胞内皮粘附分子的表达。
本文描述了一种半定量的方法,可以利用能量色散x射线微分析(EDX)来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。作为两种粘附分子的模型,E-selection (CD62E;内皮白细胞粘附分子-1 (ELAM-1)和细胞间粘附分子-1;CD54),在内毒素脂多糖(LPS)、肿瘤坏死因子(TNF)或磷酯(PMA)刺激HUVEC后,用银增强胶体金法定位。在扫描电子显微镜(SEM)下进行分析,加速电压为15 kV,扫描面积为200 x 400微米。半定量数据显示,lps处理组两种粘附分子的表达量均显著高于其他各组(P < 0.01)。此外,处理4 h后,各组e -选择素的表达水平均高于ICAM-1。将x射线微量分析的实验数据与酶联免疫吸附试验(ELISA)的数据进行比较,发现两种制剂的值相似。这种微量分析方法相对简单,似乎适用于体外不同类型内皮细胞的免疫金标记研究。
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