Tai Youyi, Brinkley Natasha, Jin Lu, Chang Yu Wei, Liakhovetski Allen, Nam Jin
Department of Bioengineering, University of California, Riverside, CA, USA.
Stem Cell Res Ther. 2025 Jul 18;16(1):385. doi: 10.1186/s13287-025-04488-y.
Neural stem cells hold significant promise for developing in vitro nerve models due to their capacity to differentiate into diverse neural cell types. While traditional biochemical approaches often restrict differentiation to a single phenotype, limiting the ability to study critical neuron-glia interactions, physical stimuli have been explored due to their capacity to drive multi-phenotypic differentiation of neural stem cells. However, underlying molecular mechanisms mediating the physical stimulation-induced neural stem cell differentiation, with an emphasis on electrical stimulation and mechanical stimulation, remain inadequately explored, hindering the comprehensive optimization and application of physical stimulation for enhanced neuromorphogenesis.
In this study, we explored the signaling pathways driving mechano-electrical stimulation-induced multi-phenotypic differentiation of NSCs using a piezoelectric platform with signaling inhibitors. The signaling knowledge was then used to further enhance the neuromorphogenesis by employing signal activator/inhibitor in combination with mechano-electrical stimulation.
We discovered that electrical stimulation promotes the neuronal differentiation of NSCs via Wnt signaling through the TRPC1 channel, while mechanical stimulation activates the TRPV4-RhoA/ROCK axis, inducing astrocytic and oligodendrocytic differentiation via JAK/Stat3 and Shh/Gli1 pathways, respectively. Targeted modulation of these pathways under mechano-electrical stimulation further enhanced neuromorphogenesis, including improved neurite outgrowth, synaptic interactions, and myelin maturation.
This study systematically uncovered the signaling cascades that mediate the mechano-electrical stimulation-induced multi-phenotypic differentiation of neural stem cells towards neurons and glial cells, which were separately mediated by electrical stimulation and mechanical stimulation, respectively, through independent signaling cascades. The combination of physical stimulation with biochemical factors to modulate those signaling pathways further enhanced neuromorphogenesis, offering a reliable and robust strategy to develop fully functional neural stem cell-derived in vitro nerve models.
神经干细胞因其能够分化为多种神经细胞类型,在体外神经模型的开发中具有巨大潜力。虽然传统的生化方法通常将分化限制在单一表型,从而限制了研究关键神经元 - 胶质细胞相互作用的能力,但由于物理刺激能够驱动神经干细胞的多表型分化,因此人们对其进行了探索。然而,介导物理刺激诱导神经干细胞分化的潜在分子机制,尤其是电刺激和机械刺激,仍未得到充分研究,这阻碍了物理刺激在增强神经形态发生方面的全面优化和应用。
在本研究中,我们使用带有信号抑制剂的压电平台,探索了驱动机械 - 电刺激诱导神经干细胞多表型分化的信号通路。然后,利用这些信号知识,通过将信号激活剂/抑制剂与机械 - 电刺激相结合,进一步增强神经形态发生。
我们发现,电刺激通过TRPC1通道经Wnt信号促进神经干细胞的神经元分化,而机械刺激激活TRPV4 - RhoA/ROCK轴,分别通过JAK/Stat3和Shh/Gli1途径诱导星形胶质细胞和少突胶质细胞分化。在机械 - 电刺激下对这些通路进行靶向调节进一步增强了神经形态发生,包括改善神经突生长、突触相互作用和髓鞘成熟。
本研究系统地揭示了介导机械 - 电刺激诱导神经干细胞向神经元和胶质细胞多表型分化的信号级联反应,它们分别由电刺激和机械刺激通过独立的信号级联反应介导。将物理刺激与生化因子相结合以调节这些信号通路进一步增强了神经形态发生,为开发功能完备的神经干细胞衍生体外神经模型提供了一种可靠且强大的策略。