Hasegawa-Sasaki H, Sasaki T
Biochim Biophys Acta. 1983 Dec 20;754(3):305-14.
The human T lymphoblastoid cell line designated CCRF-CEM responds to phytohemagglutinin with a 3.7-fold enhancement of the 32PO4 incorporation into phosphatidylinositol. In myo-[2-3H]inositol-prelabeled CCRF-CEM cells, phytohemagglutinin induced a 3.3-fold accumulation of myo-[2-3H]inositol phosphate during 15 min incubation at 37 degrees C in the presence of 5 mM LiCl. Since Li+ is a potent inhibitor of myo-inositol-1-phosphatase, the results indicate that phytohemagglutinin induces the hydrolysis of inositol lipids in CCRF-CEM cells. In 32PO4-prelabeled CCRF-CEM cells, phytohemagglutinin induced a breakdown of 28% of [32P]phosphatidylinositol 4,5-bisphosphate 40-60 s after the stimulation. The decrease of [32P]phosphatidylinositol 4,5-bisphosphate was found as early as 10 s after the stimulation. This decrease was followed by an increased 32P-labeling of phosphatidic acid. In [2-3H]glycerol-prelabeled CCRF-CEM cells, phytohemagglutinin induced a transient accumulation of [3H]phosphatidic acid and [3H]diacylglycerol. The amount of [3H]phosphatidic acid in the stimulated cells was 3.7-times the control value at 2 min after the stimulation, whereas the amount of [3H]diacylglycerol in the stimulated cells was 1.5-times the control value at 5 min after the stimulation. In [3H8]arachidonate-prelabeled CCRF-CEM cells, phytohemagglutinin induced a transient accumulation of [3H]phosphatidic acid; the amount was 2.5-times the control value at 2 min after the stimulation. Quinacrine (1 mM) caused 41% reduction in the amount of [3H]phosphatidic acid accumulated by the stimulation in [2-3H]glycerol-prelabeled cells. Stimulation in a Ca2+-free saline containing 1 mM EGTA caused 53% reduction in the amount of [3H]phosphatidic acid accumulated by the stimulation. The results presented in this paper indicate that a human T lymphoblastoid cell line, CCRF-CEM, responds to phytohemagglutinin with a rapid turnover of inositol lipids.
名为CCRF - CEM的人T淋巴母细胞系对植物血凝素产生反应,其将³²P⁰⁴掺入磷脂酰肌醇的量增加了3.7倍。在以肌醇 - [2 - ³H]预标记的CCRF - CEM细胞中,在37℃、5 mM LiCl存在的条件下孵育15分钟期间,植物血凝素诱导肌醇 - [2 - ³H]磷酸积累了3.3倍。由于Li⁺是肌醇 - 1 - 磷酸酶的有效抑制剂,结果表明植物血凝素诱导CCRF - CEM细胞中肌醇脂质的水解。在以³²P⁰⁴预标记的CCRF - CEM细胞中,刺激后40 - 60秒,植物血凝素诱导28%的[³²P]磷脂酰肌醇4,5 - 二磷酸分解。[³²P]磷脂酰肌醇4,5 - 二磷酸的减少早在刺激后10秒就被发现。这种减少之后是磷脂酸的³²P标记增加。在以[2 - ³H]甘油预标记的CCRF - CEM细胞中,植物血凝素诱导[³H]磷脂酸和[³H]二酰基甘油的短暂积累。刺激后2分钟,受刺激细胞中[³H]磷脂酸的量是对照值的3.7倍,而刺激后5分钟,受刺激细胞中[³H]二酰基甘油的量是对照值的1.5倍。在以[³H⁸]花生四烯酸预标记的CCRF - CEM细胞中,植物血凝素诱导[³H]磷脂酸的短暂积累;刺激后2分钟,其含量是对照值的2.5倍。奎纳克林(1 mM)使以[2 - ³H]甘油预标记的细胞中因刺激而积累的[³H]磷脂酸量减少了41%。在含有1 mM EGTA的无钙盐溶液中进行刺激,使因刺激而积累的[³H]磷脂酸量减少了53%。本文给出的结果表明,人T淋巴母细胞系CCRF - CEM对植物血凝素产生反应,伴随着肌醇脂质的快速周转。