Hirasawa N, Sato Y, Fujita Y, Mue S, Ohuchi K
Department of Pathophysiological Biochemistry, Faculty of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.
J Immunol. 1998 Nov 1;161(9):4939-43.
Antigen stimulation of IgE-sensitized rat basophilic leukemia RBL-2H3 cells induced activation of c-Jun N-terminal kinase (JNK) within a few minutes with maximum activity attained 40 min later. The increase in JNK activity was accompanied with an increase in phosphorylation of c-Jun in the cells. The Ag-induced JNK activation was inhibited by the phosphatidylinositol 3-kinase inhibitors wortmannin (10-100 nM) and LY 294002 (100 microM) but not by the protein kinase C inhibitors calphostin C (1 and 3 microM) and Ro 31-8425 (1 and 3 microM). Pretreatment with dexamethasone (10 and 100 nM) for 18 h inhibited the Ag-induced increase in JNK activity in a concentration-dependent manner. At least 6 h of preincubation with dexamethasone was necessary to inhibit the Ag-induced JNK activation. The phosphorylation of c-Jun induced by the Ag stimulation was reduced by pretreatment with dexamethasone without reduction of the content of c-Jun protein. The Ag-induced activation of the JNK kinase kinase mitogen-activated protein kinase-extracellular signal-regulated kinase kinase-1 was also inhibited by pretreatment with dexamethasone at 10 and 100 nM. These findings indicate that dexamethasone reduces JNK protein level and inhibits the Ag-induced activation of JNK resulting in the inhibition of c-Jun phosphorylation.
抗原刺激IgE致敏的大鼠嗜碱性白血病RBL - 2H3细胞,可在几分钟内诱导c - Jun氨基末端激酶(JNK)激活,40分钟后达到最大活性。JNK活性的增加伴随着细胞内c - Jun磷酸化的增加。抗原诱导的JNK激活被磷脂酰肌醇3激酶抑制剂渥曼青霉素(10 - 100 nM)和LY 294002(100 microM)抑制,但不被蛋白激酶C抑制剂钙泊三醇C(1和3 microM)和Ro 31 - 8425(1和3 microM)抑制。用10和100 nM地塞米松预处理18小时,以浓度依赖的方式抑制了抗原诱导的JNK活性增加。用地塞米松预孵育至少6小时对于抑制抗原诱导的JNK激活是必要的。用地塞米松预处理可降低抗原刺激诱导的c - Jun磷酸化,而不降低c - Jun蛋白含量。10和100 nM地塞米松预处理也抑制了抗原诱导的JNK激酶激酶丝裂原活化蛋白激酶 - 细胞外信号调节激酶激酶 - 1的激活。这些发现表明,地塞米松降低JNK蛋白水平并抑制抗原诱导的JNK激活,从而导致c - Jun磷酸化的抑制。