Huwiler A, Pfeilschifter J
Department of Pharmacology, Biozentrum, University of Basel, Switzerland.
FEBS Lett. 1994 Aug 15;350(1):135-8. doi: 10.1016/0014-5793(94)00754-3.
Interleukin-1 (IL-1) stimulates a time- and concentration-dependent mitogen-activated protein (MAP) kinase activation in rat mesangial cells. A rapid increase in activity (maximal at 10 min) is followed by a second persistent level of activity which steadily increases over 24 h. The second peak of MAP kinase activity is paralleled by a marked de novo synthesis of p42 MAP kinase as measured by immunoprecipitation of [35S]methionine-labelled mesangial cells and by a 60% increase in total p42 MAP kinase protein as detected by Western blot analysis. We propose that IL-1 induced de novo synthesis of p42 MAP kinase is important for the multiplicity of long-term actions of this cytokine in renal mesangial cells.
白细胞介素-1(IL-1)可刺激大鼠系膜细胞中丝裂原活化蛋白(MAP)激酶呈时间和浓度依赖性激活。活性迅速增加(10分钟时达到最大值),随后是第二个持续的活性水平,该水平在24小时内稳步上升。通过对[35S]甲硫氨酸标记的系膜细胞进行免疫沉淀测定,以及通过蛋白质印迹分析检测到总p42 MAP激酶蛋白增加60%,发现p42 MAP激酶的明显从头合成与MAP激酶活性的第二个峰值平行。我们认为,IL-1诱导的p42 MAP激酶从头合成对于该细胞因子在肾系膜细胞中的多种长期作用很重要。