Price M R, Baldwin R W
Br J Cancer. 1974 Nov;30(5):382-93. doi: 10.1038/bjc.1974.212.
Membrane fractions were isolated from homogenates of an aminoazo dye induced rat hepatoma (hepatoma D23) by sucrose density gradient centrifugation in zonal rotors. The membrane fractions retained tumour specific antigenic determinants and exhibited an increased antigenic activity over other subcellular membrane fractions, as defined by their capacity to quantitatively neutralize the membrane immunofluorescence staining of viable hepatoma D23 cells by antibody in tumour immune serum. In contrast, no antigenic activity was found to be associated with purified hepatoma D23 nuclei or nuclear membranes as evaluated by the in vitro antigen assay.The two methods described for the isolation of hepatoma D23 membranes have been developed for the large scale fractionation of tumour homogenates in order that further studies upon the nature and immunogenicity of membrane associated tumour specific antigens may be resolved using defined membrane preparations of increased antigenic activity.
通过在区带转子中进行蔗糖密度梯度离心,从氨基偶氮染料诱导的大鼠肝癌(肝癌D23)匀浆中分离出膜组分。这些膜组分保留了肿瘤特异性抗原决定簇,并且与其他亚细胞膜组分相比,表现出增强的抗原活性,这是通过它们定量中和肿瘤免疫血清中抗体对活肝癌D23细胞的膜免疫荧光染色的能力来定义的。相比之下,通过体外抗原测定评估,未发现纯化的肝癌D23细胞核或核膜具有抗原活性。所描述的两种分离肝癌D23膜的方法是为了大规模分离肿瘤匀浆而开发的,以便使用具有增强抗原活性的特定膜制剂来解决关于膜相关肿瘤特异性抗原的性质和免疫原性的进一步研究。