Cellular and Molecular Biotechnology Institute, National Institute of Advanced Industrial Science and Technology (AIST), Central 5-41, 1-1-1 Higashi, Tsukuba 305-8565, Japan.
Tsukuba Life Science Innovation Program (T-LSI), School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba 305-8572, Japan.
Int J Mol Sci. 2023 May 21;24(10):9053. doi: 10.3390/ijms24109053.
In vitro derivation of human neurons in the autonomic nervous system (ANS) is an important technology, given its regulatory roles in maintaining homeostasis in the human body. Although several induction protocols for autonomic lineages have been reported, the regulatory machinery remains largely undefined, primarily due to the absence of a comprehensive understanding of the molecular mechanism regulating human autonomic induction in vitro. In this study, our objective was to pinpoint key regulatory components using integrated bioinformatics analysis. A protein-protein interaction network construction for the proteins encoded by the differentially expressed genes from our RNA sequencing data, and conducting subsequent module analysis, we identified distinct gene clusters and hub genes involved in the induction of autonomic lineages. Moreover, we analyzed the impact of transcription factor (TF) activity on target gene expression, revealing enhanced autonomic TF activity that could lead to the induction of autonomic lineages. The accuracy of this bioinformatics analysis was corroborated by employing calcium imaging to observe specific responses to certain ANS agonists. This investigation offers novel insights into the regulatory machinery in the generation of neurons in the ANS, which would be valuable for further understanding and precise regulation of autonomic induction and differentiation.
在体外衍生人体自主神经系统(ANS)中的神经元是一项重要技术,因为它在维持人体体内平衡方面具有调节作用。尽管已经报道了几种自主谱系的诱导方案,但调节机制在很大程度上仍未得到明确,主要是因为缺乏对体外调节人类自主诱导的分子机制的全面理解。在这项研究中,我们的目标是使用集成的生物信息学分析来确定关键的调节成分。通过对我们的 RNA 测序数据中差异表达基因编码的蛋白质进行蛋白质-蛋白质相互作用网络构建,并进行随后的模块分析,我们确定了参与自主谱系诱导的不同基因簇和枢纽基因。此外,我们分析了转录因子(TF)活性对靶基因表达的影响,揭示了增强的自主 TF 活性可能导致自主谱系的诱导。通过钙成像观察对某些 ANS 激动剂的特定反应来验证这种生物信息学分析的准确性。这项研究为自主诱导和分化的精确调控提供了关于 ANS 神经元生成中调节机制的新见解。