Mårtensson Lisa, Gustavsson Per, Dahlin Lars B, Kanje Martin
Department of Cell and Organism Biology, Lund University, Lund, Sweden.
Neuroreport. 2007 Jul 2;18(10):957-61. doi: 10.1097/WNR.0b013e32819f8f27.
Activation of extracellular-signal-regulated kinase-1/2 (Erk1/2) by phosphorylation to p-Erk1/2, and proliferation of Schwann cells were investigated in the rat sciatic nerve by immunohistochemistry. Axotomy in vivo and culturing of nerve segments in vitro resulted in a rapid (30 min) increase of p-Erk1/2 in Schwann cells with peaks at 2 and 24 h. Proliferation measured by bromodeoxy uridine incorporation and immunostaining in vivo and in vitro 48 h after axotomy showed an increase in Schwann cell proliferation at the sites of Erk1/2 activation. The Erk1/2 inhibitor U0126 inhibited both the increase in p-Erk1/2 and the bromodeoxy uridine incorporation. We suggest that an increase in p-Erk1/2 is required for nerve injury-induced proliferation of Schwann cells.
通过免疫组织化学研究了磷酸化激活细胞外信号调节激酶1/2(Erk1/2)成为p-Erk1/2以及大鼠坐骨神经中雪旺细胞增殖的情况。体内轴突切断和体外神经节段培养导致雪旺细胞中p-Erk1/2迅速(30分钟)增加,在2小时和24小时达到峰值。通过溴脱氧尿苷掺入法和免疫染色测定的体内和体外轴突切断后48小时的增殖情况显示,Erk1/2激活部位的雪旺细胞增殖增加。Erk1/2抑制剂U0126抑制了p-Erk1/2的增加和溴脱氧尿苷掺入。我们认为,p-Erk1/2的增加是神经损伤诱导雪旺细胞增殖所必需的。