Tunru I S, Suzuki H, Kobayashi M
First Department of Internal Medicine, Toyama Medical and Pharmaceutical University, Japan.
Experientia. 1993 Jan 15;49(1):76-9. doi: 10.1007/BF01928795.
The induction of lymphokine-activated killer (LAK) cells from natural killer (NK) lineage cells by interleukin-4 (IL-4) was studied in vitro. Activation of nude mouse spleen cells by IL-4 generated cytotoxic cells, capable of killing NK-sensitive as well as NK-resistant tumor cells. The induction of peak lytic activity was demonstrated after 3 days of culture with IL-4. Surface marker analysis indicated that the majority of precursor cells were aGM1+, Thy1-, and the majority of effector cells were aGM1+, Thy1+, suggesting that IL-4 induced LAK cells from nude mouse spleen cells were similar to those from normal mouse spleen cells. The induction of nude mouse LAK cells by IL-4 was partially inhibited by anti-IL-4 or anti-interferon (IFN)-alpha,beta antibody, and it was further inhibited by the combination of two antibodies, suggesting that IFN-alpha,beta production was associated with LAK induction of NK lineage cells by IL-4.
在体外研究了白细胞介素-4(IL-4)从自然杀伤(NK)谱系细胞诱导淋巴因子激活的杀伤(LAK)细胞的过程。用IL-4激活裸鼠脾细胞产生了细胞毒性细胞,这些细胞能够杀伤NK敏感以及NK抗性的肿瘤细胞。在用IL-4培养3天后显示出峰值裂解活性。表面标志物分析表明,大多数前体细胞为aGM1+、Thy1-,而大多数效应细胞为aGM1+、Thy1+,这表明由IL-4诱导的来自裸鼠脾细胞的LAK细胞与来自正常小鼠脾细胞的LAK细胞相似。抗IL-4或抗干扰素(IFN)-α、β抗体可部分抑制IL-4对裸鼠LAK细胞的诱导,两种抗体联合使用时抑制作用更强,这表明IFN-α、β的产生与IL-4诱导NK谱系细胞产生LAK有关。