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出价表达网络在鸟类睫状神经节发育过程中控制神经元细胞命运。

Bid Expression Network Controls Neuronal Cell Fate During Avian Ciliary Ganglion Development.

作者信息

Koszinowski Sophie, La Padula Veronica, Edlich Frank, Krieglstein Kerstin, Busch Hauke, Boerries Melanie

机构信息

Department of Molecular Embryology, Institute of Anatomy and Cell Biology, Albert-Ludwigs-University Freiburg, Freiburg, Germany.

Faculty of Biology, Albert-Ludwigs-University Freiburg, Freiburg, Germany.

出版信息

Front Physiol. 2018 Jun 29;9:797. doi: 10.3389/fphys.2018.00797. eCollection 2018.

Abstract

Avian ciliary ganglion (CG) development involves a transient execution phase of apoptosis controlling the final number of neurons, but the time-dependent molecular mechanisms for neuronal cell fate are largely unknown. To elucidate the molecular networks regulating important aspects of parasympathetic neuronal development, a genome-wide expression analysis was performed during multiple stages of avian CG development between embryonic days E6 and E14. The transcriptome data showed a well-defined sequence of events, starting from neuronal migration via neuronal fate cell determination, synaptic transmission, and regulation of synaptic plasticity to growth factor associated signaling. In particular, we extracted a neuronal apoptosis network that characterized the cell death execution phase at E8/E9 and apoptotic cell clearance at E14 by combining the gene time series analysis with network synthesis from the chicken interactome. Network analysis identified TP53 as key regulator and predicted involvement of the BH3 interacting domain death agonist (BID). A virus-based RNAi knockdown approach showed a crucial impact of BID expression on the execution of ontogenetic programmed cell death (PCD). In contrast, Bcl-XL expression did not impact PCD. Therefore, BID-mediated apoptosis represents a novel cue essential for timing within CG maturation.

摘要

鸟类睫状神经节(CG)的发育涉及一个短暂的凋亡执行阶段,该阶段控制着神经元的最终数量,但神经元细胞命运的时间依赖性分子机制在很大程度上尚不清楚。为了阐明调节副交感神经元发育重要方面的分子网络,在胚胎第6天(E6)至第14天(E14)的鸟类CG发育的多个阶段进行了全基因组表达分析。转录组数据显示了一系列明确的事件顺序,从神经元迁移开始,经过神经元命运细胞的确定、突触传递、突触可塑性的调节,到与生长因子相关的信号传导。特别是,我们通过将基因时间序列分析与来自鸡相互作用组的网络合成相结合,提取了一个神经元凋亡网络,该网络表征了E8/E9时的细胞死亡执行阶段和E14时的凋亡细胞清除。网络分析确定TP53为关键调节因子,并预测BH3相互作用结构域死亡激动剂(BID)的参与。基于病毒的RNA干扰敲低方法表明,BID表达对个体发育程序性细胞死亡(PCD)的执行具有关键影响。相比之下,Bcl-XL表达对PCD没有影响。因此,BID介导的凋亡代表了CG成熟过程中时间安排所必需的一个新线索。

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