Le Berre-Scoul Catherine, Chevalier Julien, Oleynikova Elena, Cossais François, Talon Sophie, Neunlist Michel, Boudin Hélène
INSERM UMR 913, IMAD, University of Nantes, France.
J Physiol. 2017 Jan 15;595(2):583-598. doi: 10.1113/JP271989. Epub 2016 Aug 18.
Unlike astrocytes in the brain, the potential role of enteric glial cells (EGCs) in the formation of the enteric neuronal circuit is currently unknown. To examine the role of EGCs in the formation of the neuronal network, we developed a novel neuron-enriched culture model from embryonic rat intestine grown in indirect coculture with EGCs. We found that EGCs shape axonal complexity and synapse density in enteric neurons, through purinergic- and glial cell line-derived neurotrophic factor-dependent pathways. Using a novel and valuable culture model to study enteric neuron-glia interactions, our study identified EGCs as a key cellular actor regulating neuronal network maturation.
In the nervous system, the formation of neuronal circuitry results from a complex and coordinated action of intrinsic and extrinsic factors. In the CNS, extrinsic mediators derived from astrocytes have been shown to play a key role in neuronal maturation, including dendritic shaping, axon guidance and synaptogenesis. In the enteric nervous system (ENS), the potential role of enteric glial cells (EGCs) in the maturation of developing enteric neuronal circuit is currently unknown. A major obstacle in addressing this question is the difficulty in obtaining a valuable experimental model in which enteric neurons could be isolated and maintained without EGCs. We adapted a cell culture method previously developed for CNS neurons to establish a neuron-enriched primary culture from embryonic rat intestine which was cultured in indirect coculture with EGCs. We demonstrated that enteric neurons grown in such conditions showed several structural, phenotypic and functional hallmarks of proper development and maturation. However, when neurons were grown without EGCs, the complexity of the axonal arbour and the density of synapses were markedly reduced, suggesting that glial-derived factors contribute strongly to the formation of the neuronal circuitry. We found that these effects played by EGCs were mediated in part through purinergic P2Y receptor- and glial cell line-derived neurotrophic factor-dependent pathways. Using a novel and valuable culture model to study enteric neuron-glia interactions, our study identified EGCs as a key cellular actor required for neuronal network maturation.
与大脑中的星形胶质细胞不同,肠胶质细胞(EGC)在肠神经元回路形成中的潜在作用目前尚不清楚。为了研究EGC在神经网络形成中的作用,我们从与EGC间接共培养的胚胎大鼠肠道中开发了一种新型的富含神经元的培养模型。我们发现,EGC通过嘌呤能和胶质细胞系衍生的神经营养因子依赖性途径塑造肠神经元的轴突复杂性和突触密度。利用一种新颖且有价值的培养模型来研究肠神经元与胶质细胞的相互作用,我们的研究确定EGC是调节神经网络成熟的关键细胞因子。
在神经系统中,神经元回路的形成是内在和外在因素复杂而协调作用的结果。在中枢神经系统中,星形胶质细胞衍生的外在介质已被证明在神经元成熟中起关键作用,包括树突塑形、轴突导向和突触形成。在肠神经系统(ENS)中,肠胶质细胞(EGC)在发育中的肠神经元回路成熟中的潜在作用目前尚不清楚。解决这个问题的一个主要障碍是难以获得一个有价值的实验模型,在该模型中可以分离并维持肠神经元而不含有EGC。我们采用了先前为中枢神经系统神经元开发的细胞培养方法,从胚胎大鼠肠道中建立了一种富含神经元的原代培养物,并与EGC进行间接共培养。我们证明,在这种条件下生长的肠神经元表现出正常发育和成熟的几个结构、表型和功能特征。然而,当神经元在没有EGC的情况下生长时,轴突分支的复杂性和突触密度明显降低,这表明胶质细胞衍生的因子对神经元回路的形成有很大贡献。我们发现,EGC发挥的这些作用部分是通过嘌呤能P2Y受体和胶质细胞系衍生的神经营养因子依赖性途径介导的。利用一种新颖且有价值的培养模型来研究肠神经元与胶质细胞的相互作用,我们的研究确定EGC是神经网络成熟所需的关键细胞因子。