Suppr超能文献

一种用于隔离的体外测定法:恶性疟原虫感染的红细胞与福尔马林固定的内皮细胞和无黑色素黑色素瘤细胞的结合。

An in vitro assay for sequestration: binding of Plasmodium falciparum-infected erythrocytes to formalin-fixed endothelial cells and amelanotic melanoma cells.

作者信息

Udeinya I J, Leech J, Aikawa M, Miller L H

出版信息

J Protozool. 1985 Feb;32(1):88-90. doi: 10.1111/j.1550-7408.1985.tb03019.x.

Abstract

Erythrocytes infected with Plasmodium falciparum bind specifically to cultured endothelial cells and to a line of amelanotic melanoma cells. We have fixed endothelial cells and amelanotic melanoma cells in various ways and determined whether the fixed cells were still able to bind infected erythrocytes. Only cells fixed with 1.0-2.5% formalin in phosphate-buffered saline continued to bind infected erythrocytes as well as unfixed cells. The mechanism of binding to fixed and unfixed cells appeared to be identical for the following reasons. First, erythrocytes infected by parasite strains that bound to unfixed cells also bound to fixed cells while those that did not bind to unfixed cells did not bind to fixed cells. Second, immune serum that inhibited binding to unfixed cells also inhibited binding to fixed cells. Third, electron microscopy showed that knobs were the points of attachment between infected erythrocytes and both fixed and unfixed melanoma cells. Fixed cells gave reproducible results over at least 2 months. Thus, we have developed a simplified, reproducible assay for measuring binding of P. falciparum-infected erythrocytes to target cells.

摘要

感染恶性疟原虫的红细胞能特异性地结合培养的内皮细胞以及一株无黑色素生成的黑色素瘤细胞系。我们用多种方法固定内皮细胞和无黑色素生成的黑色素瘤细胞,并确定固定后的细胞是否仍能结合感染的红细胞。只有在磷酸盐缓冲盐水中用1.0 - 2.5%福尔马林固定的细胞,才能像未固定的细胞一样继续结合感染的红细胞。由于以下原因,与固定和未固定细胞结合的机制似乎是相同的。第一,被能结合未固定细胞的寄生虫株感染的红细胞也能结合固定细胞,而那些不能结合未固定细胞的则不能结合固定细胞。第二,抑制与未固定细胞结合的免疫血清也能抑制与固定细胞的结合。第三,电子显微镜显示,微小突起是感染的红细胞与固定和未固定的黑色素瘤细胞之间的附着点。固定细胞在至少2个月内给出了可重复的结果。因此,我们开发了一种简化的、可重复的检测方法,用于测量恶性疟原虫感染的红细胞与靶细胞的结合。

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