Goldman R, Zor U
Department of Membrane Research & Biophysics, Weizmann Institute of Science, Rehovot, Israel.
Biochem Biophys Res Commun. 1994 Feb 28;199(1):334-8. doi: 10.1006/bbrc.1994.1233.
Phorbol ester (TPA) is generally considered to be a negative regulator of PtdIns-PLC activity. Here we show, for the first time, that the combination of TPA+ vanadate is a positive regulator (activator) of PtdIns-PLC in mouse elicited peritoneal macrophages. Vanadate or TPA on their own had no effect on PtdIns-PLC activity. In addition, TPA+ vanadate enhanced reactive oxygen species formation and protein tyrosine phosphorylation. PtdIns-PLC activation was suppressed by down regulation or inhibition of PKC, by inhibition of NADPH oxidase activity and scavenging of its product, and by inhibitors of protein tyrosine kinase activity. We conclude that PKC activation by TPA in the presence of vanadate activates the formation of reactive oxygen species, which are essential for the enhancement of protein tyrosine phosphorylation and eventually to PtdIns-PLC activation.
佛波酯(TPA)通常被认为是磷脂酰肌醇磷脂酶C(PtdIns-PLC)活性的负调节因子。在此我们首次表明,TPA与钒酸盐的组合是小鼠诱导腹腔巨噬细胞中PtdIns-PLC的正调节因子(激活剂)。单独的钒酸盐或TPA对PtdIns-PLC活性没有影响。此外,TPA+钒酸盐增强了活性氧的形成和蛋白质酪氨酸磷酸化。通过下调或抑制蛋白激酶C(PKC)、抑制NADPH氧化酶活性并清除其产物以及使用蛋白质酪氨酸激酶活性抑制剂,可抑制PtdIns-PLC的激活。我们得出结论,在钒酸盐存在的情况下,TPA激活PKC,进而激活活性氧的形成,活性氧对于增强蛋白质酪氨酸磷酸化并最终激活PtdIns-PLC至关重要。