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肿瘤坏死因子α/肿瘤坏死因子受体2信号传导是背根进入区胶质细胞包裹所必需的。

TNFa/TNFR2 signaling is required for glial ensheathment at the dorsal root entry zone.

作者信息

Smith Cody J, Wheeler Michael A, Marjoram Lindsay, Bagnat Michel, Deppmann Christopher D, Kucenas Sarah

机构信息

Department of Biology, University of Virginia, Charlottesville, Virginia, United States of America.

Neuroscience Graduate Program, University of Virginia, Charlottesville, Virginia, United States of America.

出版信息

PLoS Genet. 2017 Apr 5;13(4):e1006712. doi: 10.1371/journal.pgen.1006712. eCollection 2017 Apr.

Abstract

Somatosensory information from the periphery is routed to the spinal cord through centrally-projecting sensory axons that cross into the central nervous system (CNS) via the dorsal root entry zone (DREZ). The glial cells that ensheath these axons ensure rapid propagation of this information. Despite the importance of this glial-axon arrangement, how this afferent nerve is assembled during development is unknown. Using in vivo, time-lapse imaging we show that as centrally-projecting pioneer axons from dorsal root ganglia (DRG) enter the spinal cord, they initiate expression of the cytokine TNFalpha. This induction coincides with ensheathment of these axons by associated glia via a TNF receptor 2 (TNFR2)-mediated process. This work identifies a signaling cascade that mediates peripheral glial-axon interactions and it functions to ensure that DRG afferent projections are ensheathed after pioneer axons complete their navigation, which promotes efficient somatosensory neural function.

摘要

来自外周的躯体感觉信息通过向中枢投射的感觉轴突传递至脊髓,这些轴突经背根进入区(DREZ)进入中枢神经系统(CNS)。包裹这些轴突的神经胶质细胞确保了该信息的快速传播。尽管这种神经胶质-轴突排列很重要,但在发育过程中传入神经是如何组装的尚不清楚。我们利用活体延时成像技术发现,当来自背根神经节(DRG)的向中枢投射的先驱轴突进入脊髓时,它们会启动细胞因子TNFα的表达。这种诱导与相关神经胶质细胞通过肿瘤坏死因子受体2(TNFR2)介导的过程包裹这些轴突同时发生。这项研究确定了一个介导外周神经胶质-轴突相互作用的信号级联反应,其作用是确保在先驱轴突完成导航后DRG传入投射被包裹,从而促进高效的躯体感觉神经功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8f8/5397050/64f827c138e7/pgen.1006712.g001.jpg

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