Deppert W, Hanke K, Henning R
J Virol. 1980 Aug;35(2):505-18. doi: 10.1128/JVI.35.2.505-518.1980.
Simian virus 40 (SV40)-transformed monolayer cells were analyzed in situ by indirect immunofluorescence microscopy for the postulated cell surface location of SV40 T-antigen-related molecules. With antisera prepared against purified, sodium dodecyl sulfate-denatured SV40 T-antigen, positive surface staining was obtained when the cells had been treated with formaldehyde before immunofluorescence analysis. In contrast, living SV40-transformed cells analyzed in monolayer were surface fluorescence negative. The fixation procedure developed in this study combined with a double staining immunofluorescence technique allowed the simultaneous analysis of the same cells for the expression of both SV40 T-antigen-related surface antigen and nuclear T-antigen. The localization of SV40 T-antigen-related surface antigen on the outer surface of the plasma membrane of formaldehyde-fixed SV40-transformed cells was demonstrated directly by the protein A-mediated binding of Staphylococcus aureus bacteria on formaldehyde-fixed SV40-transformed cells precoated with antiserum against sodium dodecyl sulfate-denatured T-antigen. Both cell surface staining and S. aureus binding were found to be highly specific for SV40 T-antigen-related binding sites. These results indicate that T-antigen-related molecules in a cryptic form are located on the surface of SV40-transformed monolayer cells and can be detected in situ after modification of the cell surface architecture.
通过间接免疫荧光显微镜对猴病毒40(SV40)转化的单层细胞进行原位分析,以确定SV40 T抗原相关分子在假定的细胞表面位置。用针对纯化的十二烷基硫酸钠变性的SV40 T抗原制备的抗血清,在免疫荧光分析前用甲醛处理细胞时可获得阳性表面染色。相比之下,单层分析的活SV40转化细胞表面荧光为阴性。本研究开发的固定程序与双重染色免疫荧光技术相结合,可对同一细胞同时分析SV40 T抗原相关表面抗原和核T抗原的表达。通过蛋白A介导的金黄色葡萄球菌与预先用抗十二烷基硫酸钠变性T抗原的抗血清包被的甲醛固定的SV40转化细胞的结合,直接证明了SV40 T抗原相关表面抗原在甲醛固定的SV40转化细胞质膜外表面的定位。发现细胞表面染色和金黄色葡萄球菌结合对SV40 T抗原相关结合位点具有高度特异性。这些结果表明,以隐蔽形式存在的T抗原相关分子位于SV40转化的单层细胞表面,并且在细胞表面结构改变后可在原位检测到。