Brown G, Turner B M, Morris C J, Bahman A M, Fisher A G, Whitfield W G, Davies S, Barthakur R, Johnson G D
Eur J Cell Biol. 1985 Nov;39(1):86-96.
The monoclonal antibody, AGF2.3, was isolated from mice immunised with the human promyeloid cell line HL60. By immunofluorescence and immunoelectron microscopy the antibody was shown to bind to the nuclear envelope in uninduced HL60 cells. Immunofluorescent staining was reduced to very low levels in HL60 cells induced to mature to monocytes or neutrophils by addition of 12-0-tetradecanoylphorbol-13-acetate or dimethyl sulfoxide respectively. Blood neutrophils did not express the antigen. Weak immunofluorescent staining of cell nuclei was observed in peripheral blood lymphocytes and in sections of normal human kidney, tonsil and skin epithelium. The AGF2.3 antigen was strongly expressed on the nuclei of 21/21 haemopoietic cell lines and 21/25 permanent non-haemopoietic cell lines representing various cell types. In contrast, the antigen was not expressed by any of six primary (untransformed) cell cultures. These included fibroblasts, endothelial cells and keratinocytes. The antigen was expressed in the Q10 SV-40 transformed cell line derived from a non-expressing primary fibroblast culture. AGF2.3 antibody precipitated a protein with an apparent subunit molecular weight of approximately 215 kDa from Triton X-100 extracts of HL60 and HeLa cells labelled with 35S-methionine. This protein was not detectable in extracts of primary skin fibroblasts prepared in parallel. We conclude that AGF2.3 antibody recognises a previously undescribed protein associated with the nuclear envelope which is expressed at high levels in most transformed cell lines but which is weakly expressed or absent in normal tissues and primary cell cultures.
单克隆抗体AGF2.3是从用人早幼粒细胞系HL60免疫的小鼠中分离得到的。通过免疫荧光和免疫电子显微镜观察,该抗体在未诱导的HL60细胞中可与核膜结合。分别添加12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯或二甲基亚砜诱导HL60细胞成熟为单核细胞或中性粒细胞后,免疫荧光染色降低至极低水平。血液中的中性粒细胞不表达该抗原。在外周血淋巴细胞以及正常人肾脏、扁桃体和皮肤上皮组织切片中观察到细胞核有微弱的免疫荧光染色。AGF2.3抗原在代表各种细胞类型的21/21个造血细胞系和21/25个永久性非造血细胞系的细胞核上强烈表达。相比之下,六种原代(未转化)细胞培养物均不表达该抗原。这些细胞包括成纤维细胞、内皮细胞和角质形成细胞。该抗原在源自非表达性原代成纤维细胞培养物的Q10 SV - 40转化细胞系中表达。AGF2.3抗体从用35S - 甲硫氨酸标记的HL60和HeLa细胞的Triton X - 100提取物中沉淀出一种表观亚基分子量约为215 kDa的蛋白质。在平行制备的原代皮肤成纤维细胞提取物中未检测到这种蛋白质。我们得出结论,AGF2.3抗体识别一种与核膜相关的此前未描述的蛋白质,该蛋白质在大多数转化细胞系中高水平表达,但在正常组织和原代细胞培养物中弱表达或不表达。