Liu Xiaoyu, Peng Su, Zhao Yahong, Zhao Tingting, Wang Meihong, Luo Lan, Yang Yumin, Sun Cheng
Jiangsu Key Laboratory of Neuroregeneration, Co-innovation Center of Neuroregeneration, Nantong University, 19 Qixiu Road, Nantong, Jiangsu, 226001, People's Republic of China.
Department of Geratology, Affiliated Hospital of Nantong University, Nantong, 226001, Jiangsu, China.
Mol Neurobiol. 2017 Jul;54(5):3554-3564. doi: 10.1007/s12035-016-9913-3. Epub 2016 May 18.
The process of Schwann cells (SCs) forming a sheath around axons is termed as myelination, which plays a pivotal role for proper physiological function in the peripheral nervous system (PNS). The molecular mechanisms regulating SC myelination in the PNS remain to be elucidated. Here, we show that AMP-activated protein kinase (AMPK) in sciatic nerves was gradually decreased during the PNS myelination process. Pharmacological interventions showed that activation of AMPK by AICAR attenuated myelin gene expression in SCs, whereas inhibition of AMPK by Compound C (ComC) or AMPKα1 knockdown stimulated myelin gene expression. Following experiments revealed that c-Jun, a negative modulator of PNS myelination, was activated by AMPK in SCs. The application of ComC in newborn rats markedly downregulated c-Jun expression in sciatic nerves. The lipid and protein synthesis in sciatic nerves was greatly potentiated by ComC. As a consequence, myelin gene expression in sciatic nerves, as well as myelin sheath thickness, were promoted in the ComC-treated rats. All together, our data identify that AMPK is an important negative regulator of Schwann cell myelination in the PNS, and this regulation role may rely on c-Jun activation.
施万细胞(SCs)在轴突周围形成髓鞘的过程被称为髓鞘形成,这对周围神经系统(PNS)的正常生理功能起着关键作用。调节PNS中施万细胞髓鞘形成的分子机制仍有待阐明。在此,我们表明坐骨神经中的AMP激活蛋白激酶(AMPK)在PNS髓鞘形成过程中逐渐减少。药理学干预表明,AICAR激活AMPK会减弱施万细胞中髓鞘基因的表达,而Compound C(ComC)抑制AMPK或敲低AMPKα1则会刺激髓鞘基因表达。后续实验表明,PNS髓鞘形成的负调节因子c-Jun在施万细胞中被AMPK激活。在新生大鼠中应用ComC可显著下调坐骨神经中c-Jun的表达。ComC可极大地增强坐骨神经中的脂质和蛋白质合成。因此,在ComC处理的大鼠中,坐骨神经中的髓鞘基因表达以及髓鞘厚度均得到促进。总之,我们的数据表明AMPK是PNS中施万细胞髓鞘形成的重要负调节因子,且这种调节作用可能依赖于c-Jun的激活。