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神经营养因子-4通过TrkB/PI3K/Akt/mTORC1信号通路诱导培养的施万细胞中髓鞘蛋白零的表达。

Neurotrophin-4 induces myelin protein zero expression in cultured Schwann cells via the TrkB/PI3K/Akt/mTORC1 pathway.

作者信息

Guo Wei, Li Yan, Sun Chao, Duan Hui-Quan, Liu Shen, Xu Yun-Qiang, Feng Shi-Qing

机构信息

Department of Orthopaedics, Tianjin Medical University General Hospital, Tianjin, People's Republic of China.

出版信息

Anim Cells Syst (Seoul). 2017 Feb 21;21(2):84-92. doi: 10.1080/19768354.2017.1289980. eCollection 2017.

Abstract

Myelin formation during peripheral nervous system development, as well as myelin repair after injury and in disease, requires multiple intrinsic and extrinsic signals. Neurotrophin-4 (NT-4) is a member of the neurotrophin family, which regulates the development of neuronal networks by participating in the growth of neuronal processes, synaptic development and plasticity, neuronal survival, and differentiation. However, the intracellular signaling pathways by which NT-4 participates in myelination by Schwann cells remain elusive. In this study, we examined the effects of NT-4 on the expression of compact myelin proteins in cultured Schwann cells. Using real-time quantitative RT-PCR and western blotting, we found that NT-4 could significantly enhance the expression of myelin protein zero (MPZ) but not the expression of myelin basic protein or peripheral myelin protein 22. Further, knockdown of truncated TrkB with small interfering RNA could eliminate the effect of NT-4 on MPZ expression. Moreover, we demonstrated that the NT-4-enhanced MPZ expression depended on Akt and mTORC1 signaling. Taken together, these results suggest that NT-4 binds TrkB to enhance the expression of MPZ in Schwann cells, probably through the PI3K/Akt/mTORC1 signaling pathway, thus contributing to myelination.

摘要

外周神经系统发育过程中的髓鞘形成,以及损伤后和疾病状态下的髓鞘修复,都需要多种内在和外在信号。神经营养因子-4(NT-4)是神经营养因子家族的一员,它通过参与神经元突起的生长、突触发育和可塑性、神经元存活及分化来调节神经网络的发育。然而,NT-4参与施万细胞髓鞘形成的细胞内信号通路仍不清楚。在本研究中,我们检测了NT-4对培养的施万细胞中紧密髓鞘蛋白表达的影响。通过实时定量逆转录聚合酶链反应和蛋白质免疫印迹法,我们发现NT-4能显著增强髓鞘蛋白零(MPZ)的表达,但不影响髓鞘碱性蛋白或外周髓鞘蛋白22的表达。此外,用小干扰RNA敲低截短型TrkB可消除NT-4对MPZ表达的影响。而且,我们证明NT-4增强的MPZ表达依赖于Akt和mTORC1信号通路。综上所述,这些结果表明NT-4与TrkB结合,可能通过PI3K/Akt/mTORC1信号通路增强施万细胞中MPZ的表达,从而促进髓鞘形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e8e/6138314/3c677cc2913d/TACS_A_1289980_F0001_C.jpg

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