Engel K, Ahlers A, Brach M A, Herrmann F, Gaestel M
Max-Delbrück-Center for Molecular Medicine, Berlin, Germany.
J Cell Biochem. 1995 Feb;57(2):321-30. doi: 10.1002/jcb.240570216.
The activation of MAPKAP kinase 2 was investigated under heat-shock conditions in mouse Ehrlich ascites tumor cells and after treatment of human MO7 cells with tumor necrosis factor-alpha (TNF-alpha). MAPKAP kinase 2 activity was determined using the small heat-shock proteins (sHsps) Hsp25 and Hsp27 as substrates. In both cell types, about a threefold increase in MAPKAP kinase 2 activity could be detected in a time interval of about 10-15 min after stimulation either by heat shock or TNF-alpha. Phosphorylation of MAPKAP kinase 2, but not the level of MAPKAP kinase 2 mRNA, was increased after heat shock in EAT cells. It is further shown that activation of MAPKAP kinase 2 in MO7 cells is accompanied by increased MAP kinase activity. These data strongly suggest that increased phosphorylation of the sHsps after heat shock or TNF-alpha treatment results from phosphorylation by MAPKAP kinase 2, which itself is activated by phosphorylation through MAP kinases. Hence, we demonstrate that MAPKAP kinase 2 is responsible not only for phosphorylation of sHsps in vitro but also in vivo. The findings link sHsp phosphorylation to the MAP kinase cascade, explaining the early phosphorylation of sHsp that is stimulated by a variety of inducers such as mitogens, phorbol esters, thrombin, calcium ionophores, and heat shock.
在热休克条件下,对小鼠艾氏腹水瘤细胞以及用肿瘤坏死因子-α(TNF-α)处理人MO7细胞后,研究了丝裂原活化蛋白激酶相关激酶2(MAPKAP激酶2)的激活情况。使用小分子热休克蛋白(sHsps)Hsp25和Hsp27作为底物来测定MAPKAP激酶2的活性。在这两种细胞类型中,热休克或TNF-α刺激后约10 - 15分钟的时间间隔内,均可检测到MAPKAP激酶2的活性增加约三倍。在艾氏腹水瘤细胞中,热休克后MAPKAP激酶2的磷酸化增加,但MAPKAP激酶2 mRNA的水平未增加。进一步表明,MO7细胞中MAPKAP激酶2的激活伴随着丝裂原活化蛋白激酶(MAP激酶)活性的增加。这些数据有力地表明,热休克或TNF-α处理后sHsps磷酸化增加是由MAPKAP激酶2磷酸化所致,而MAPKAP激酶2本身是通过MAP激酶磷酸化而被激活的。因此,我们证明MAPKAP激酶2不仅在体外而且在体内都负责sHsps的磷酸化。这些发现将sHsp磷酸化与MAP激酶级联反应联系起来,解释了由多种诱导剂如促分裂原、佛波酯、凝血酶、钙离子载体和热休克刺激引起的sHsp早期磷酸化现象。