Steen V M, Tysnes O B, Holmsen H
Department of Biochemistry, University of Bergen, Norway.
Biochem J. 1989 Oct 15;263(2):621-4. doi: 10.1042/bj2630621.
The [32P]PIP2/[32P]PA and the [32P]PIP/[32P]PA relationships were demonstrated to be remarkably similar after stimulation of [32P]Pi-prelabelled platelets for 90 s with various combinations and concentrations of agonists and inhibitors. Thus the activity of the PI and PIP kinases with the corresponding phosphomonoesterases may be tightly controlled during receptor-mediated platelet stimulation involving phospholipase C activation.
在用各种激动剂和抑制剂的组合及浓度对[32P]Pi预标记的血小板刺激90秒后,[32P]PIP2/[32P]PA和[32P]PIP/[32P]PA的关系被证明非常相似。因此,在涉及磷脂酶C激活的受体介导的血小板刺激过程中,PI和PIP激酶与相应磷酸单酯酶的活性可能受到严格控制。