Lin P, Fung S J, Li S, Chen T, Repetto B, Huang K S, Gilfillan A M
Department of Bronchopulmonary Research, Hoffmann-La Roche Inc., Nutley, NJ 07110.
Biochem J. 1994 Apr 1;299 ( Pt 1)(Pt 1):109-14. doi: 10.1042/bj2990109.
We explored the possible role of tyrosine kinases in the IgE-dependent regulation of 1,2-diacylglycerol (DAG) production in RBL 2H3 cells. When triggered via their high-affinity IgE receptors (Fc epsilon RI), there was a rapid phosphorylation of tyrosine residues on a number of proteins. The phosphorylation of these proteins and ultimately histamine release were inhibited in a concentration-dependent manner by the tyrosine kinase inhibitor, tyrphostin. In cells labelled with [3H]myristic acid, we observed a characteristic biphasic increase in [3H]DAG production. In the presence of tyrosine kinase inhibitor, the initial increase in DAG was still observed, but the secondary increase, which was dependent on phosphatidylcholine-specific phospholipase D (PC-PLD) activation, was completely abolished. Tyrphostin significantly inhibited IgE-dependent activation of PC-PLD, suggesting that PC-PLD activation was regulated by tyrosine phosphorylation. Furthermore, when proteins from RBL 2H3 cells were immunoprecipitated with an anti-phosphotyrosine antibody, PC-PLD activity was recovered from the immunoprecipitated fraction. These results demonstrate that the secondary, but not the initial, phase of 1,2-DAG production in response to Fc epsilon RI aggregation is regulated by the initial activation of tyrosine kinases and that PC-PLD may be regulated directly by this mechanism.
我们探究了酪氨酸激酶在RBL 2H3细胞中1,2 - 二酰甘油(DAG)产生的IgE依赖性调节中的可能作用。当通过其高亲和力IgE受体(FcεRI)触发时,许多蛋白质上的酪氨酸残基会迅速磷酸化。酪氨酸激酶抑制剂 tyrphostin以浓度依赖性方式抑制这些蛋白质的磷酸化以及最终的组胺释放。在用[3H]肉豆蔻酸标记的细胞中,我们观察到[3H]DAG产生呈现出典型的双相增加。在存在酪氨酸激酶抑制剂的情况下,仍可观察到DAG的初始增加,但依赖于磷脂酰胆碱特异性磷脂酶D(PC-PLD)激活的二次增加则完全被消除。Tyrphostin显著抑制了IgE依赖性的PC-PLD激活,这表明PC-PLD的激活受酪氨酸磷酸化调节。此外,当用抗磷酸酪氨酸抗体对RBL 2H3细胞中的蛋白质进行免疫沉淀时,PC-PLD活性可从免疫沉淀部分中恢复。这些结果表明,响应FcεRI聚集时1,2 - DAG产生的第二阶段而非初始阶段受酪氨酸激酶的初始激活调节,并且PC-PLD可能直接受此机制调节。