Gomez D E, Hartzler J L, Corbitt R H, Nason A M, Thorgeirsson U P
Division of Cancer Etiology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
In Vitro Cell Dev Biol Anim. 1993 Jun;29A(6):451-5.
We describe a fast and reproducible method that can be used as a final step in obtaining pure populations of liver endothelial cells. This method employs endothelial cell specific lectin covalently bound to magnetic polystyrene beads (Dynabeads). Evonymus europaeus agglutinin (EEA)-coated Dynabeads were used to purify monkey liver endothelium from Percoll gradient separated nonparenchymal cells. EEA-coated beads were also successfully used to purify monkey aortic endothelial cells. The endothelial cells grew to confluence as a cobblestonelike monolayer, expressed Factor VIII related antigen, and incorporated acetylated-low density lipoprotein. The magnetic beads seemed not to modify the normal properties of the isolated endothelium, thus facilitating their use in experimental studies. This immunomagnetic separation technique may be applicable for purification of endothelial cells from a wide variety of tissue sources.
我们描述了一种快速且可重复的方法,该方法可作为获得纯肝内皮细胞群体的最后一步。此方法采用与磁性聚苯乙烯珠( Dynabeads )共价结合的内皮细胞特异性凝集素。用欧洲卫矛凝集素(EEA)包被的 Dynabeads 从经 Percoll 梯度分离的非实质细胞中纯化猴肝内皮细胞。EEA包被的磁珠也成功用于纯化猴主动脉内皮细胞。内皮细胞生长至汇合形成鹅卵石样单层,表达因子 VIII 相关抗原,并摄取乙酰化低密度脂蛋白。磁珠似乎未改变分离出的内皮细胞的正常特性,从而便于其在实验研究中的应用。这种免疫磁分离技术可能适用于从多种组织来源中纯化内皮细胞。