Akiba S, Hatazawa R, Ono K, Hayama M, Matsui H, Sato T
Department of Pathological Biochemistry, Kyoto Pharmaceutical University, Misasagi, Yamashina-ku, Kyoto 607-8414, Japan.
Br J Pharmacol. 2000 Nov;131(5):1004-10. doi: 10.1038/sj.bjp.0703637.
The regulatory effects of transforming growth factor (TGF)-alpha on phospholipase A(2) (PLA(2)) isozymes contributing to prostaglandin generation in rat gastric epithelial RGM1 cells were examined. Stimulation with TGF-alpha for 24 h time-dependently induced prostaglandin E(2) generation with an increase in cyclo-oxygenase-2 protein. The TGF-alpha-induced prostaglandin E(2) generation was suppressed by NS-398, a cyclo-oxygenase-2 inhibitor. TGF-alpha stimulated the activity and the protein synthesis of cytosolic PLA(2) (cPLA(2)). A time-dependent increase in cPLA(2) protein occurred in parallel with PGE(2) generation, which was inhibited by methyl arachidonyl fluorophosphonate (MAFP), a cPLA(2) inhibitor. However, no change in activity of secretory PLA(2) or Ca(+2)-independent PLA(2) was observed in the TGF-alpha-stimulated cells. Stimulation with the Ca(2+) ionophore A23187 for 10 min induced MAFP-sensitive arachidonic acid liberation. Interestingly, preincubation with TGF-alpha for 24 h diminished A23187-stimulated arachidonic acid liberation despite the increase in cPLA(2) protein. Under the conditions, TGF-alpha was found to increase p11, an endogenous cPLA(2) suppressor, also known as annexin II light chain. The TGF-alpha-induced increase in p11 was suppressed by tyrphostin AG1478, an inhibitor of tyrosine kinase of epidermal growth factor receptor, which was also found to restore the inhibition by TGF-alpha of A23187-stimulated arachidonic acid liberation. However, TGF-alpha did not alter protein levels of annexin II heavy chain. These results suggest that TGF-alpha stimulates prostaglandin generation through an increase in cPLA(2), the hydrolytic action of which may be under the control of p11.
研究了转化生长因子(TGF)-α对大鼠胃上皮RGM1细胞中参与前列腺素生成的磷脂酶A(2)(PLA(2))同工酶的调节作用。用TGF-α刺激24小时,随着环氧化酶-2蛋白的增加,前列腺素E(2)的生成呈时间依赖性诱导。环氧化酶-2抑制剂NS-398可抑制TGF-α诱导的前列腺素E(2)生成。TGF-α刺激了胞质型磷脂酶A(2)(cPLA(2))的活性和蛋白质合成。cPLA(2)蛋白的时间依赖性增加与PGE(2)生成平行,而cPLA(2)抑制剂甲基花生四烯酰氟磷酸酯(MAFP)可抑制这种增加。然而,在TGF-α刺激的细胞中,分泌型磷脂酶A(2)或非钙依赖性磷脂酶A(2)的活性未观察到变化。用钙离子载体A23187刺激10分钟可诱导MAFP敏感的花生四烯酸释放。有趣的是,尽管cPLA(2)蛋白增加,但用TGF-α预孵育24小时可减少A23187刺激的花生四烯酸释放。在这些条件下,发现TGF-α可增加p11,一种内源性cPLA(2)抑制剂,也称为膜联蛋白II轻链。表皮生长因子受体酪氨酸激酶抑制剂 tyrphostin AG1478可抑制TGF-α诱导的p11增加,同时也发现其可恢复TGF-α对A23187刺激的花生四烯酸释放的抑制作用。然而,TGF-α并未改变膜联蛋白II重链的蛋白水平。这些结果表明,TGF-α通过增加cPLA(2)刺激前列腺素生成,其水解作用可能受p11的控制。