van Rooijen N, Poppema A
Department of Cell Biology, Faculty of Medicine, Free University, Amsterdam, The Netherlands.
J Pharmacol Toxicol Methods. 1992 Dec;28(4):217-21. doi: 10.1016/1056-8719(92)90007-n.
In earlier studies, we described a technique for the "in vivo" depletion of macrophages, using liposome-encapsulated dichloromethylene bisphosphonate (C12MBP). The aim of the present study was to compare the effects on macrophages of various other liposome-delivered Ca2+ chelators: EDTA, DTPA, and EGTA. It appeared that both EDTA and DTPA as well as Ca(2+)-and Cu(2+)-EDTA complexes were also effective in the elimination of splenic macrophages when encapsulated in liposomes and intravenously injected. EGTA, a well-known and frequently used Ca2+ chelator, had no effect.
在早期研究中,我们描述了一种使用脂质体包裹的二氯亚甲基二膦酸盐(C12MBP)“体内”清除巨噬细胞的技术。本研究的目的是比较其他各种脂质体递送的Ca2+螯合剂(乙二胺四乙酸(EDTA)、二乙三胺五乙酸(DTPA)和乙二醇双四乙酸(EGTA))对巨噬细胞的影响。结果显示,当EDTA、DTPA以及Ca(2 +)-和Cu(2 +)-EDTA复合物包裹在脂质体中并静脉注射时,它们在清除脾脏巨噬细胞方面同样有效。EGTA是一种广为人知且常用的Ca2+螯合剂,却没有效果。