Watanabe R, Munemasa T, Matsumura M, Fujimaki M
New Product Research Laboratories II, Daiichi Pharmaceutical Co., Ltd., Edogawa-Ku, Tokyo, Japan.
Methods Find Exp Clin Pharmacol. 2007 Jun;29(5):321-7. doi: 10.1358/mf.2007.29.5.1117556.
The potential of newly formulated fluorescent-labeled liposomes for the intravital staining of Kupffer cells was evaluated in rats. Fluorescently labeled phosphatidylcholine (PC) was incorporated into liposomes consisting of PC and phosphatidylserine. After intravenous injection, Kupffer cells in the rat liver were intravitally stained and were clearly delineated under the fluorescence image of both confocal laser scanning microscopy and in vivo microscopy. Specificity of the staining was confirmed by immunohistochemistry using the anti-rat macrophage antibody Ki-M2R, which suggested that the liposomes were selectively entrapped by the hepatic reticuloendothelial system. A time-course study revealed that the suitable observation window was between 16 and 24 h after the injection. Phagocytic activity of Kupffer cells after the administration of liposomes was examined by measuring the amount of hepatic uptake of intravenously administered fluorescent microspheres; no detrimental influence of the liposomes on the phagocytic activity was observed. Additionally, no histopathologic changes were found in the livers from liposome-treated rats. Therefore, the fluorescent-labeled liposomes appear to be a useful research tool for labeling Kupffer cells for in vivo microscopic observation of the liver.
在大鼠中评估了新制备的荧光标记脂质体对库普弗细胞进行活体染色的潜力。将荧光标记的磷脂酰胆碱(PC)掺入由PC和磷脂酰丝氨酸组成的脂质体中。静脉注射后,大鼠肝脏中的库普弗细胞被活体染色,并在共聚焦激光扫描显微镜和体内显微镜的荧光图像下清晰可见。使用抗大鼠巨噬细胞抗体Ki-M2R通过免疫组织化学证实了染色的特异性,这表明脂质体被肝网状内皮系统选择性摄取。一项时间进程研究表明,合适的观察窗口是在注射后16至24小时之间。通过测量静脉注射的荧光微球的肝脏摄取量来检查脂质体给药后库普弗细胞的吞噬活性;未观察到脂质体对吞噬活性有不利影响。此外,在接受脂质体治疗的大鼠肝脏中未发现组织病理学变化。因此,荧光标记的脂质体似乎是一种用于标记库普弗细胞以进行肝脏体内显微镜观察的有用研究工具。