Greene G L, Nolan C, Engler J P, Jensen E V
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5115-9. doi: 10.1073/pnas.77.9.5115.
Extranuclear estrogen receptor protein (estrophilin) of MCF-7 human breast cancer cells was purified by passage of the cytosol fraction of a cell homogenate through an affinity column of estradiol linked to Sepharose by a substituted di-n-propyl sulfide bridge in the 17 alpha position. Elution with 50 micro M [3H]estradiol in 10% (vol/vol) dimethyl formamide/0.5 M sodium thiocyanate gave 40% recovery of [3H]estradiol-estrophilin showing 14% of the specific radioactivity expected for the pure complex. Serum from a Lewis rat immunized with this partially purified estradiol-receptor complex contained antiestrophilin antibodies that reacted not only with nuclear and extranuclear estradiol-receptor complexes from MCF-7 cells but also with estrophilin from rat, calf, and monkey uterus, hen oviduct, and human breast cancers. Splenic lymphocytes from the immunized rat were fused with cells of two different mouse myeloma lines (P3-X63-Ag8 and Sp2/0-Ag14) to yield hybridoma cultures, 2% of which produced antibodies to estrophilin. After cloning by limiting dilution, three hybridoma lines secreting antiestrophilin were expanded in suspension culture and as ascites tumors in athymic mice to provide substantial quantities of monoclonal antibodies that recognize mammalian but not avian estrophilin and that show different degrees of reactivity with receptor from nonprimate sources. By growing the clone from Sp2/0 in the presence of [35S]methionine, radiolabeled monoclonal IgG has been prepared. These monoclonal antibodies should prove useful in the study of estrogen receptors of human reproductive tissues, in particular for the radioimmunochemical assay and immunocytochemical localization of receptors in breast cancers.
通过将细胞匀浆的胞质溶胶部分通过由17α位的取代二正丙基硫醚桥连接到琼脂糖的雌二醇亲和柱,对MCF-7人乳腺癌细胞的核外雌激素受体蛋白(雌激素亲和蛋白)进行纯化。用10%(体积/体积)二甲基甲酰胺/0.5M硫氰酸钠中的50μM[3H]雌二醇洗脱,[3H]雌二醇-雌激素亲和蛋白的回收率为40%,显示出纯复合物预期比放射性的14%。用这种部分纯化的雌二醇受体复合物免疫的Lewis大鼠血清中含有抗雌激素亲和蛋白抗体,该抗体不仅与MCF-7细胞核内和核外的雌二醇受体复合物反应,还与大鼠、小牛和猴子子宫、母鸡输卵管以及人类乳腺癌中的雌激素亲和蛋白反应。将免疫大鼠的脾淋巴细胞与两种不同的小鼠骨髓瘤细胞系(P3-X63-Ag8和Sp2/0-Ag14)的细胞融合,产生杂交瘤培养物,其中2%产生抗雌激素亲和蛋白的抗体。通过有限稀释克隆后,将三个分泌抗雌激素亲和蛋白的杂交瘤细胞系在悬浮培养中扩增,并在无胸腺小鼠中作为腹水肿瘤扩增以提供大量单克隆抗体,这些抗体识别哺乳动物而非禽类的雌激素亲和蛋白,并且与非灵长类来源的受体表现出不同程度的反应性。通过在[35S]甲硫氨酸存在下培养来自Sp系的克隆,制备了放射性标记的单克隆IgG。这些单克隆抗体在人类生殖组织雌激素受体的研究中应会证明有用,特别是用于乳腺癌中受体的放射免疫化学测定和免疫细胞化学定位。