Beh K J, Haynes S E, Ward K A
Mol Immunol. 1986 Jul;23(7):717-24. doi: 10.1016/0161-5890(86)90082-9.
Two mouse X sheep interspecific cell hybrids were obtained by fusing mouse myeloma cell line Sp2/O. Ag14 with sheep lymphocytes obtained from a lymph node antigenically stimulated with azo-benzene arsonate-ovalbumin (ABA-ova). The interspecific cell lines were characterized using immunochemical, karyotypic and molecular DNA techniques. Both cell lines secreted sheep IgG1 antibody specific for the ABA haptenic determinant. Karyotypic analysis revealed that cell lines 4.11 and 11.9 had modal chromosome numbers of 91 and 106, respectively. Although C-banded spreads confirmed that fusion between sheep and mouse cells had occurred, it was not possible to differentiate sheep from mouse chromosomes. However, DNA hybridization techniques showed that each line contained sheep repetitive sequence DNA. It was calculated that cell line 11.9 contained 17640 copies while cell line 4.11 contained 734 copies of the previously characterized sheep satellite DNA.
通过将小鼠骨髓瘤细胞系Sp2/O.Ag14与从用偶氮苯砷酸盐 - 卵清蛋白(ABA - ova)抗原刺激的淋巴结获得的绵羊淋巴细胞融合,获得了两个小鼠×绵羊种间细胞杂种。使用免疫化学、核型分析和分子DNA技术对种间细胞系进行了表征。两个细胞系都分泌针对ABA半抗原决定簇的绵羊IgG1抗体。核型分析表明,4.11和11.9细胞系的染色体众数分别为91和106。虽然C带涂片证实绵羊和小鼠细胞之间发生了融合,但无法区分绵羊和小鼠染色体。然而,DNA杂交技术表明每个细胞系都含有绵羊重复序列DNA。据计算,11.9细胞系含有17640个先前表征的绵羊卫星DNA拷贝,而4.11细胞系含有734个拷贝。