Liao Yumei, Zhuang Xiaoji, Huang Xiaojie, Peng Yinghui, Ma Xuanyue, Huang Zhi-Xing, Liu Feng, Xu Junyu, Wang Ying, Chen Wei-Min, Ye Wen-Cai, Shi Lei
JNU-HKUST Joint Laboratory for Neuroscience and Innovative Drug Research, Jinan University, Guangzhou, China.
College of Pharmacy, Jinan University, Guangzhou, China.
Front Pharmacol. 2018 Apr 5;9:290. doi: 10.3389/fphar.2018.00290. eCollection 2018.
Developing therapeutic approaches that target neuronal differentiation will be greatly beneficial for the regeneration of neurons and synaptic networks in neurological diseases. Protein synthesis (mRNA translation) has recently been shown to regulate neurogenesis of neural stem/progenitor cells (NSPCs). However, it has remained unknown whether engineering translational machinery is a valid approach for manipulating neuronal differentiation. The present study identifies that a bivalent securinine compound SN3-L6, previously designed and synthesized by our group, induces potent neuronal differentiation through a novel translation-dependent mechanism. An isobaric tag for relative and absolute quantitation (iTRAQ)-based proteomic analysis in Neuro-2a progenitor cells revealed that SN3-L6 upregulated a group of neurogenic transcription regulators, and also upregulated proteins involved in RNA processing, translation, and protein metabolism. Notably, puromycylation and metabolic labeling of newly synthesized proteins demonstrated that SN3-L6 induced rapid and robust activation of general mRNA translation. Importantly, mRNAs of the proneural transcription factors Foxp1, Foxp4, Hsf1, and Erf were among the targets that were translationally upregulated by SN3-L6. Either inhibition of translation or knockdown of these transcription factors blocked SN3-L6 activity. We finally confirmed that protein synthesis of a same set of transcription factors was upregulated in primary cortical NPCs. These findings together identify a new compound for translational activation and neuronal differentiation, and provide compelling evidence that reprogramming transcriptional regulation network at translational levels is a promising strategy for engineering NSPCs.
开发针对神经元分化的治疗方法将对神经疾病中神经元和突触网络的再生大有裨益。蛋白质合成(mRNA翻译)最近已被证明可调节神经干/祖细胞(NSPCs)的神经发生。然而,工程化翻译机制是否是操纵神经元分化的有效方法仍不清楚。本研究发现,我们小组先前设计并合成的一种二价一叶萩碱化合物SN3-L6,通过一种新的翻译依赖性机制诱导强大的神经元分化。基于等量异位标签相对和绝对定量(iTRAQ)的Neuro-2a祖细胞蛋白质组分析显示,SN3-L6上调了一组神经源性转录调节因子,还上调了参与RNA加工、翻译和蛋白质代谢的蛋白质。值得注意的是,新合成蛋白质的嘌呤霉素化和代谢标记表明,SN3-L6诱导了一般mRNA翻译的快速而强烈的激活。重要的是,神经前体转录因子Foxp1、Foxp4、Hsf1和Erf的mRNA是被SN3-L6翻译上调的靶标之一。翻译抑制或这些转录因子的敲低均阻断了SN3-L6的活性。我们最终证实,在原代皮质NPC中,同一组转录因子的蛋白质合成上调。这些发现共同确定了一种用于翻译激活和神经元分化的新化合物,并提供了令人信服的证据,即在翻译水平上重新编程转录调控网络是工程化NSPCs的一种有前途的策略。