Okano F, Tachibana H, Akiyama K, Shirahata S, Murakami H
Graduate School of Genetic Resources Technology, Kyushu University, Fukuoka, Japan.
Cytotechnology. 1993;11(3):205-11. doi: 10.1007/BF00749871.
Immortalized human T cell lines were established by cotransfecting c-Ha-ras and c-myc oncogenes to lymph node lymphocytes. The cell lines kept growing for 3 months after establishment without a decrease in growth rate. The cells did not require interleukin-2 (IL-2) for their growth, but addition of IL-2 stimulated the growth of these cells. Flow cytometric analysis revealed that these cells were T cells expressing CD4 or CD8 antigens. A CD4 positive (CD4+) cell line produced IL-6, indicating that the cell line belongs to helper T cells. The CD8 positive (CD8+) cell line possessed cytotoxicity to tumor cells, indicating that the cell line were killer T cells. Both cell lines were able to proliferate in serum-free medium indefinitely.
通过将c-Ha-ras和c-myc癌基因共转染至淋巴结淋巴细胞,建立了永生化人T细胞系。细胞系建立后持续生长3个月,生长速率没有下降。这些细胞生长不需要白细胞介素-2(IL-2),但添加IL-2可刺激这些细胞生长。流式细胞术分析显示,这些细胞是表达CD4或CD8抗原的T细胞。一个CD4阳性(CD4+)细胞系产生IL-6,表明该细胞系属于辅助性T细胞。CD8阳性(CD8+)细胞系对肿瘤细胞具有细胞毒性,表明该细胞系是杀伤性T细胞。两个细胞系都能够在无血清培养基中无限增殖。