Suppr超能文献

在体内,趋化因子诱导白细胞与血管内皮细胞牢固黏附,这严重依赖于白细胞最初的滚动。

Chemoattractant-induced firm adhesion of leukocytes to vascular endothelium in vivo is critically dependent on initial leukocyte rolling.

作者信息

Lindbom L, Xie X, Raud J, Hedqvist P

机构信息

Department of Physiology I, Karolinska Institute, Stockholm, Sweden.

出版信息

Acta Physiol Scand. 1992 Dec;146(4):415-21. doi: 10.1111/j.1748-1716.1992.tb09442.x.

Abstract

Leukocyte rolling and firm adhesion at the venular endothelium are two discrete events in the cellular inflammatory response mediated via selectin and integrin adhesion molecules, respectively. The dependency of chemoattractant-induced firm leukocyte adhesion on the preceding rolling interaction was investigated in rat mesenteric microvessels through use of intravital microscopy. Leukocyte rolling was dose-dependently inhibited by systemic treatment with the sulphated polysaccharide fucoidin. The firm leukocyte adhesion following stimulation with the chemotactic peptide fMLP was similarly inhibited when fMLP challenge was performed subsequent to inhibition of leukocyte rolling by fucoidin. Thus, based on paired observations in single venules before and after fucoidin treatment, reduced rolling leukocyte flux prior to fMLP challenge was paralleled over a wide range by a proportional decrease in fMLP-induced leukocyte adhesion. The results demonstrate quantitatively a close relationship between the extent of leukocyte rolling and the magnitude of the subsequent firm adhesion response, and, that an initial rolling interaction is a precondition for firm adhesion to occur at physiological blood flow rates in vivo.

摘要

白细胞在小静脉内皮细胞处的滚动和牢固黏附是细胞炎症反应中分别通过选择素和整合素黏附分子介导的两个不同事件。通过活体显微镜观察,研究了趋化因子诱导的白细胞牢固黏附对先前滚动相互作用的依赖性。在大鼠肠系膜微血管中,全身应用硫酸化多糖岩藻依聚糖可剂量依赖性地抑制白细胞滚动。当在岩藻依聚糖抑制白细胞滚动后进行趋化肽fMLP刺激时,fMLP刺激后白细胞的牢固黏附同样受到抑制。因此,基于岩藻依聚糖处理前后单个小静脉中的配对观察,在fMLP刺激前滚动白细胞通量的降低在很大范围内与fMLP诱导的白细胞黏附的成比例下降平行。结果定量地证明了白细胞滚动程度与随后牢固黏附反应强度之间的密切关系,并且初始滚动相互作用是在体内生理血流速率下发生牢固黏附的先决条件。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验