Offermanns S, Bombien E, Schultz G
Institut für Pharmakologie, Freie Universität Berlin, Germany.
Biochem J. 1993 Feb 15;290 ( Pt 1)(Pt 1):27-32. doi: 10.1042/bj2900027.
The proteinase thrombin, known to act via heptahelical G-protein-coupled receptors, is a mitogenic agent for different cell types, including the mouse muscle cell line BC3H1. In this study, the effect of thrombin on tyrosine phosphorylation was examined using anti-phosphotyrosine antibodies. Thrombin was found to induce phosphorylation of 65-70 and 110-120 kDa proteins in BC3H1 cells. The effect of thrombin was concentration-dependent, being half-maximal and maximal at concentrations of 0.03 and 1 unit/ml respectively. The thrombin-induced increase in phosphorylation was rapid (< or = 10 s) and transient, with a peak response after about 1-2 min. The effect of thrombin could be mimicked by the thrombin receptor agonist peptide SFLLRN-NH2. Preincubation of cells with pertussis toxin (PT) had no effect on thrombin-induced tyrosine phosphorylation. Epidermal growth factor, platelet-derived growth factor and insulin stimulated tyrosine phosphorylation of different proteins, among which were 65-70 and 110-120 kDa proteins. The phorbol ester 12-myristate 13-acetate (PMA) as well as the Ca2+ ionophore A23187 both stimulated tyrosine phosphorylation of proteins identical to those phosphorylated by thrombin, suggesting that activation of protein kinase C (PKC) and elevation of the cytosolic Ca2+ concentration alone are sufficient to induce tyrosine phosphorylation. However, calphostin C and other PKC inhibitors, which completely inhibited tyrosine phosphorylation induced by PMA, had no influence on the effect of thrombin, whereas loading of cells with the intracellular Ca2+ chelator bis-(O-aminophenoxy)ethane-NNN'N'-tetra-acetic acid totally blocked thrombin-stimulated tyrosine phosphorylation. Thus tyrosine phosphorylation stimulated by thrombin is an early PT-insensitive cellular response which is either directly mediated by elevation of cytosolic Ca2+ concentration or by a presently unknown mechanism that requires an elevated cytosolic Ca2+ concentration.
已知蛋白酶凝血酶通过七螺旋G蛋白偶联受体发挥作用,它是包括小鼠肌肉细胞系BC3H1在内的不同细胞类型的促有丝分裂剂。在本研究中,使用抗磷酸酪氨酸抗体检测了凝血酶对酪氨酸磷酸化的影响。发现凝血酶可诱导BC3H1细胞中65 - 70 kDa和110 - 120 kDa蛋白质的磷酸化。凝血酶的作用呈浓度依赖性,分别在0.03和1单位/毫升的浓度下达到半数最大效应和最大效应。凝血酶诱导的磷酸化增加迅速(≤10秒)且短暂,约1 - 2分钟后达到峰值反应。凝血酶受体激动剂肽SFLLRN - NH2可模拟凝血酶的作用。用百日咳毒素(PT)预孵育细胞对凝血酶诱导的酪氨酸磷酸化没有影响。表皮生长因子、血小板衍生生长因子和胰岛素可刺激不同蛋白质的酪氨酸磷酸化,其中包括65 - 70 kDa和110 - 120 kDa蛋白质。佛波酯12 - 肉豆蔻酸13 - 乙酸酯(PMA)以及Ca2 +离子载体A23187均刺激与凝血酶磷酸化的蛋白质相同的蛋白质的酪氨酸磷酸化,这表明蛋白激酶C(PKC)的激活和胞质Ca2 +浓度的升高单独就足以诱导酪氨酸磷酸化。然而,完全抑制PMA诱导的酪氨酸磷酸化的钙泊三醇C和其他PKC抑制剂对凝血酶的作用没有影响,而用细胞内Ca2 +螯合剂双(O - 氨基苯氧基)乙烷 - NNN'N' - 四乙酸加载细胞则完全阻断了凝血酶刺激的酪氨酸磷酸化。因此,凝血酶刺激的酪氨酸磷酸化是一种早期的PT不敏感细胞反应,它要么直接由胞质Ca2 +浓度的升高介导,要么由目前未知的需要升高的胞质Ca2 +浓度的机制介导。