Shah F J, Caviglia C, Zór K, Carminati M, Ferrari G, Sampietro M, Martínez-Serrano A, Emnéus J K, Heiskanen A R
Department of Micro- and Nanotechnology, Technical University of Denmark, Produktionstorvet, Building 423, 2800 Kongens Lyngby, Denmark.
Particle Analytical ApS, Agern Allé 3, 2970 Hørsholm, Denmark.
J Electr Bioimpedance. 2021 Nov 20;12(1):34-49. doi: 10.2478/joeb-2021-0006. eCollection 2021 Jan.
We present here the first impedance-based characterization of the differentiation process of two human mesencephalic fetal neural stem lines. The two dopaminergic neural stem cell lines used in this study, Lund human mesencephalic (LUHMES) and human ventral mesencephalic (hVM1 Bcl-X), have been developed for the study of Parkinsonian pathogenesis and its treatment using cell replacement therapy. We show that if only relying on impedance magnitude analysis, which is by far the most usual approach in, e.g., cytotoxicity evaluation and drug screening applications, one may not be able to distinguish whether the neural stem cells in a population are proliferating or differentiating. However, the presented results highlight that equivalent circuit analysis can provide detailed information on cellular behavior, e.g. simultaneous changes in cell morphology, cell-cell contacts, and cell adhesion during formation of neural projections, which are the fundamental behavioral differences between proliferating and differentiating neural stem cells. Moreover, our work also demonstrates the sensitivity of impedance-based monitoring with capability to provide information on changes in cellular behavior in relation to proliferation and differentiation. For both of the studied cell lines, in already two days (one day after induction of differentiation) equivalent circuit analysis was able to show distinction between proliferation and differentiation conditions, which is significantly earlier than by microscopic imaging. This study demonstrates the potential of impedance-based monitoring as a technique of choice in the study of stem cell behavior, laying the foundation for screening assays to characterize stem cell lines and testing the efficacy epigenetic control.
我们在此展示了对两个人类中脑胎儿神经干细胞系分化过程基于阻抗的首次表征。本研究中使用的两种多巴胺能神经干细胞系,隆德人类中脑(LUHMES)和人类腹侧中脑(hVM1 Bcl-X),是为研究帕金森病发病机制及其使用细胞替代疗法的治疗而开发的。我们表明,如果仅依靠阻抗幅度分析,这是迄今为止在例如细胞毒性评估和药物筛选应用中最常用的方法,可能无法区分群体中的神经干细胞是在增殖还是在分化。然而,所呈现的结果突出表明,等效电路分析可以提供有关细胞行为的详细信息,例如在神经突起形成过程中细胞形态、细胞间接触和细胞黏附的同时变化,这些是增殖和分化的神经干细胞之间的基本行为差异。此外,我们的工作还证明了基于阻抗监测的灵敏度,其能够提供有关细胞行为与增殖和分化相关变化的信息。对于所研究的两种细胞系,在两天内(诱导分化一天后)等效电路分析就能够显示增殖和分化状态之间的差异,这比通过显微镜成像要早得多。这项研究证明了基于阻抗监测作为干细胞行为研究中首选技术的潜力,为表征干细胞系和测试表观遗传控制功效的筛选试验奠定了基础。