Matveeva V A, Kliuchareva T E, Uvarova E N
Biull Eksp Biol Med. 1993 Feb;115(2):193-4.
Active PGE--secretion by malignant tumour cells of Syrian hamsters was demonstrated 30 min after their contact with NK-cells in vitro. The duration of PGE--secretion depended upon the ratio of tumour cells and NK--cells, engaged in contact. Increase of the number of NK--cells (bound to tumour cells) up to 10:1-20:1 led to rapid release of PGE from majority of tumour cells; in this case PGE release was continued not longer than 1.5-2.0 hours. The active release of PGE can be stopped after the contact of tumour and NK--cells by indomethacin at any moment of its secretion.
叙利亚仓鼠恶性肿瘤细胞与自然杀伤细胞(NK细胞)在体外接触30分钟后,即表现出前列腺素E2(PGE₂)的活性分泌。PGE₂分泌的持续时间取决于参与接触的肿瘤细胞与NK细胞的比例。将(与肿瘤细胞结合的)NK细胞数量增加至10:1 - 20:1会导致大多数肿瘤细胞迅速释放PGE₂;在这种情况下,PGE₂的释放持续时间不超过1.5 - 2.0小时。在肿瘤细胞与NK细胞接触后,在PGE₂分泌的任何时刻,通过吲哚美辛均可停止其活性释放。