Kirsch Matthias, Terheggen Ulrich, Hofmann Hans-Dieter
Institute of Anatomy, University of Freiburg, P.O. Box 111, D-79001 Freiburg, Germany.
Mol Cell Neurosci. 2003 Sep;24(1):130-8. doi: 10.1016/s1044-7431(03)00130-1.
To investigate the involvement of ciliary neurotropic factor (CNTF) in the postlesional response of motoneurons, we studied the activation of STAT3 signaling, the main signal transduction pathway of CNTF-like cytokines, in the facial nucleus of wildtype and CNTF-deficient mice following peripheral nerve transection. As shown by immunocytochemistry and immunoblot analysis, phosphorylation and nuclear translocation of STAT3 was maximally induced within 12 h postlesion in motoneurons of the ipsilateral facial nucleus of wildtype mice and is maintained for at least 3 days. In CNTF(-/-) mouse mutants, activation of STAT3 signaling was delayed by 10-12 h. Application of CNTF to the transected nerve restored rapid STAT3 activation in CNTF-deficient animals, whereas application of colchicine suppressed STAT3 signaling in wildtype mice for at least 24 h. These results identify CNTF as an early retrograde signal in axotomized facial motoneurons by showing that CNTF released at the lesion site is responsible for the initial induction of STAT3 signaling. Other cytokines like leukemia inhibitory factor obviously become active at later time points.
为了研究睫状神经营养因子(CNTF)在运动神经元损伤后反应中的作用,我们研究了野生型和CNTF缺陷型小鼠外周神经横断后,CNTF样细胞因子的主要信号转导途径STAT3信号通路的激活情况。免疫细胞化学和免疫印迹分析显示,野生型小鼠同侧面神经核运动神经元中,STAT3的磷酸化和核转位在损伤后12小时内被最大程度诱导,并持续至少3天。在CNTF(-/-)小鼠突变体中,STAT3信号通路的激活延迟了10 - 12小时。将CNTF应用于横断神经可恢复CNTF缺陷动物中STAT3的快速激活,而应用秋水仙碱可抑制野生型小鼠中的STAT3信号通路至少24小时。这些结果表明,损伤部位释放的CNTF负责STAT3信号通路的初始诱导,从而确定CNTF为轴突切断的面神经运动神经元中的早期逆行信号。其他细胞因子如白血病抑制因子显然在更晚的时间点才变得活跃。