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同时分析黏附于人类微血管内皮细胞的外周血粒细胞、淋巴细胞和单核细胞。

Simultaneous analysis of peripheral blood granulocytes, lymphocytes, and monocytes adhering to human microvascular endothelial cells.

作者信息

Heckmann M, Pirthauer M

机构信息

Department of Dermatology, Ludwig-Maximilians-University, Munich, Germany

出版信息

Microvasc Res. 1996 Sep;52(2):101-14. doi: 10.1006/mvre.1996.0047.

Abstract

We describe a sensitive, reliable, and convenient procedure to assay cell adhesion based on flow cytometry which allows quantitative studies of all major peripheral blood leukocytes adhering to microvascular endothelial cells. Using this assay, we show that adhesion of mononuclear cells is significantly increased in the presence of granulocytes and that maximal quantitative adhesion of lymphocytes and monocytes requires 30-40 min compared to 5-10 min required for maximal granulocyte adhesion. Moreover, we demonstrate peripheral blood leukocytes from different healthy individuals displayed considerable variations in efficiency of adhesion to pooled microvascular endothelial cells. The here-described methodology may provide a useful tool to characterize the impact of defined mediators or pharmacological agents on stable cell-cell adhesion of peripheral blood leukocytes to microvascular endothelial cells. Moreover, it may hell to identify interindividual variations in cell adhesion efficiency relevant to cell-mediated immune reactions.

摘要

我们描述了一种基于流式细胞术检测细胞黏附的灵敏、可靠且便捷的方法,该方法可对所有主要外周血白细胞与微血管内皮细胞的黏附进行定量研究。使用此检测方法,我们发现粒细胞存在时单核细胞的黏附显著增加,淋巴细胞和单核细胞的最大定量黏附需要30 - 40分钟,而粒细胞最大黏附则需要5 - 10分钟。此外,我们证明来自不同健康个体的外周血白细胞在与汇集的微血管内皮细胞黏附效率上存在相当大的差异。本文所述方法可能为表征特定介质或药物制剂对外周血白细胞与微血管内皮细胞稳定细胞间黏附的影响提供有用工具。此外,它可能有助于识别与细胞介导的免疫反应相关的细胞黏附效率的个体间差异。

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