Imanishi J, Hoshino S, Matsuoka H, Uemura H, Imanishi T, Tanaka A, Nishino H, Kishida T
Cancer Res. 1983 Sep;43(9):4323-6.
KB cells from a human nasopharyngeal tumor were cocultivated with human embryonic fibroblasts (HF 8101 cells); 7 to 14 days after incubation, "spongy degeneration"-like changes developed in the target cell-growing area. These changes developed in other target cells [HeLa cells from human cervical cancer, human hepatoma cells (PLC/PRF/5), and human amnion FL cells] cocultured with several kinds of human embryonic fibroblasts [HF 8101 cells, HF 8103 cells, and HEL cells]; however, HF 8101 cells did not cause degenerative changes in murine L929 cells. The degenerative changes were enhanced by treatment with human leukocyte interferon or human fibroblast interferon at a dose of 1,000 or 10,000 IU/ml, but there was no significant difference in the enhancing effect between human leukocyte and human fibroblast interferons. Mouse L929 interferon did not enhance the degenerative changes in KB cells caused by HF 8101 cells. It was concluded that human fibroblasts caused the degenerative changes in the human tumor cells and the continuous cell line and that the changes were enhanced by treatment with either human leukocyte interferon or human fibroblast interferon.
将来自人类鼻咽癌的KB细胞与人胚胎成纤维细胞(HF 8101细胞)共同培养;培养7至14天后,在靶细胞生长区域出现了“海绵状变性”样变化。在与几种人类胚胎成纤维细胞[HF 8101细胞、HF 8103细胞和HEL细胞]共同培养的其他靶细胞[来自人类宫颈癌的HeLa细胞、人类肝癌细胞(PLC/PRF/5)和人类羊膜FL细胞]中也出现了这些变化;然而,HF 8101细胞并未引起小鼠L929细胞的退行性变化。用1000或10000 IU/ml剂量的人白细胞干扰素或人成纤维细胞干扰素处理可增强退行性变化,但人白细胞干扰素和人成纤维细胞干扰素之间的增强效果无显著差异。小鼠L929干扰素并未增强HF 8101细胞引起的KB细胞退行性变化。得出的结论是,人成纤维细胞导致了人类肿瘤细胞和连续细胞系中的退行性变化,并且用人白细胞干扰素或人成纤维细胞干扰素处理可增强这些变化。