Watanabe N, Neda H, Ohtsuka Y, Sone H, Yamauchi N, Umetsu T, Niitsu Y, Urushizaki I
Gan To Kagaku Ryoho. 1987 Mar;14(3 Pt 1):611-7.
The internalization process and intracellular distribution of 125I-labeled TNF, in L-M (murine tumorigenic fibroblasts, highly sensitive to TNF cytotoxicity) cells and in HEL (human embryonic lung cells, non-sensitive to TNF cytotoxicity) cells bearing TNF receptor, were elucidated by pulse-chasing and by Percoll density gradient centrifugation. Effect of TNF treatment on the RNA and protein synthesis of target cells was also studied using 3H-UDR and 35S-methionine incorporation. In both L-M and HEL cells, receptor-bound 125I-TNF was rapidly internalized and delivered to lysosomes within 15-30 min, followed by degradation and release into the culture medium. RNA synthesis and protein synthesis were not affected by TNF treatment in HEL cells, but marked stimulation (3.5 times and 4.2 times, respectively) was observed in L-M cells.
通过脉冲追踪和Percoll密度梯度离心法,阐明了携带肿瘤坏死因子(TNF)受体的L-M细胞(对TNF细胞毒性高度敏感的小鼠致瘤性成纤维细胞)和HEL细胞(对TNF细胞毒性不敏感的人胚肺细胞)中125I标记的TNF的内化过程和细胞内分布。还使用3H-尿苷(3H-UDR)掺入和35S-甲硫氨酸掺入研究了TNF处理对靶细胞RNA和蛋白质合成的影响。在L-M细胞和HEL细胞中,与受体结合的125I-TNF均在15 - 30分钟内迅速内化并传递至溶酶体,随后降解并释放到培养基中。TNF处理对HEL细胞的RNA合成和蛋白质合成没有影响,但在L-M细胞中观察到明显的刺激作用(分别为3.5倍和4.2倍)。