Kazakov V K, Rosochacki S J, Ignat'eva T V, Golinskiĭ G F, Smirnov A F
Tsitologiia. 1994;36(4):372-7.
An immunocytochemical analysis of hormonal status of transgenic rats containing human growth hormone gene has been done. The enhanced expression of the endogenous growth hormone gene was demonstrated with poly- and monoclonal antibodies inside somatatropes of pituitary. No activity of the heterologous growth hormone gene was revealed in kidney, pancreas or liver as it might be expected according to specificity of MT1 and TAT promotors. Transgenic animals of F0, F1 and F2 generation exhibited disturbance of functional morphology of glucagon and insulin producing cells. Lymphocyte infiltration was found in pancreatic islets. The transgenic rabbits and swine with the gene of releasing factor of human growth hormone did not reveal any severe disturbance. Although one swine demonstrated alterations in glucagon producing cells and one rabbit revealed a disturbed morphology of the stomach tissues. The data are discussed in relation to general problems of transgene activity and interaction with endogenous homolog.
对含有人生长激素基因的转基因大鼠的激素状态进行了免疫细胞化学分析。在内分泌生长激素细胞内,用多克隆和单克隆抗体证实了内源性生长激素基因的表达增强。正如根据MT1和TAT启动子的特异性所预期的那样,在肾脏、胰腺或肝脏中未发现异源生长激素基因的活性。F0、F1和F2代转基因动物的胰高血糖素和胰岛素产生细胞的功能形态出现紊乱。在胰岛中发现淋巴细胞浸润。携带人生长激素释放因子基因的转基因兔和猪未显示出任何严重紊乱。尽管有一头猪的胰高血糖素产生细胞出现改变,一只兔子的胃组织形态出现紊乱。结合转基因活性和与内源性同源物相互作用的一般问题对数据进行了讨论。