Unité Mixte de Recherche 8194, Centre National de la Recherche Scientifique, University Paris Descartes, 75270 Paris Cedex 06, France.
Proc Natl Acad Sci U S A. 2012 Mar 6;109(10):3973-8. doi: 10.1073/pnas.1121367109. Epub 2012 Feb 21.
Glycogen synthase kinase 3β (GSK3β) inhibitors, especially the mood stabilizer lithium chloride, are also used as neuroprotective or anti-inflammatory agents. We studied the influence of LiCl on the remyelination of peripheral nerves. We showed that the treatment of adult mice with LiCl after facial nerve crush injury stimulated the expression of myelin genes, restored the myelin structure, and accelerated the recovery of whisker movements. LiCl treatment also promoted remyelination of the sciatic nerve after crush. We also demonstrated that peripheral myelin gene MPZ and PMP22 promoter activities, transcripts, and protein levels are stimulated by GSK3β inhibitors (LiCl and SB216763) in Schwann cells as well as in sciatic and facial nerves. LiCl exerts its action in Schwann cells by increasing the amount of β-catenin and provoking its nuclear localization. We showed by ChIP experiments that LiCl treatment drives β-catenin to bind to T-cell factor/lymphoid-enhancer factor response elements identified in myelin genes. Taken together, our findings open perspectives in the treatment of nerve demyelination by administering GSK3β inhibitors such as lithium.
糖原合酶激酶 3β(GSK3β)抑制剂,特别是心境稳定剂氯化锂,也被用作神经保护或抗炎药物。我们研究了氯化锂对周围神经髓鞘再生的影响。我们发现,面神经挤压损伤后,用氯化锂治疗成年小鼠可刺激髓鞘基因的表达,恢复髓鞘结构,并加速胡须运动的恢复。氯化锂处理还促进了挤压后坐骨神经的髓鞘再生。我们还证明,GSK3β 抑制剂(氯化锂和 SB216763)在施万细胞以及坐骨神经和面神经中可刺激外周髓鞘基因 MPZ 和 PMP22 启动子活性、转录物和蛋白水平。氯化锂通过增加β-连环蛋白的含量并促使其核定位在施万细胞中发挥作用。我们通过 ChIP 实验表明,氯化锂处理可促使β-连环蛋白与鉴定为髓鞘基因的 T 细胞因子/淋巴增强因子反应元件结合。总之,我们的研究结果为通过给予 GSK3β 抑制剂(如锂)治疗神经脱髓鞘开辟了新的前景。