三维细胞培养系统中的电监测方法:在体外无标签、高时空分辨率和高内容数据收集

Yagmur Demircan Yalcin, Regina Luttge
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引用次数: 9

摘要

三维(3D)细胞培养比二维(2D)细胞培养更能模拟细胞的自然环境,从而获得体内细胞间和细胞内的反应。然而,三维给细胞培养带来了复杂性。因此,3D高分辨率/高含量筛选是这类细胞培养最重要的挑战之一。虽然光学监测技术在2D领域已经得到了完善,但也可以用于监测3D细胞培养,但它们通常是终点性的、静态的、时间效率低的和劳动密集型的。或者,电传感可以成为实现二维和三维细胞培养中细胞动态、实时和无标签监测的解决方案。细胞培养电监测的发展导致了新的方法,通过将2D电技术的基本原理应用于3D以获得高时空系统。在这篇综述中,我们将这些方法分为五大类:(i) 3D阻抗测量方法;(ii)电阻抗断层扫描;(iii) 3D微电极阵列方法;(iv) 3D纳米电子学支架方法;以及(v)微物理测量。我们还定义了电子监测技术适应3D培养的挑战,并根据具体应用和技术观点解释了可能的解决方案,包括我们小组特有的方法。总之,细胞培养中的3D电监测相当具有挑战性,但最近由于微制造技术、生物工程和材料科学的重大进步,电监测的速度大大加快。本文综述的新方法具有很大的潜力,并为进一步发展找到适合(生物)医疗需求的解决方案提供了机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrical monitoring approaches in 3-dimensional cell culture systems: Toward label-free, high spatiotemporal resolution, and high-content data collection in vitro

3-dimensional (3D) cell cultures better mimic natural environment of cells than 2-dimensional (2D) cell cultures to obtain in vivo like inter and intracellular responses. However, third dimension brings complexity to cell culture. Therefore, high-resolution/high-content screening in 3D is one of the most important challenges with this type of cell cultures. Although optical monitoring techniques, well-established in 2D area, are enhanced to monitor 3D cell cultures, they are generally endpoint, static, time inefficient, and labor intensive. Alternatively, electrical sensing can become a solution to achieve dynamic, real-time, and label-free monitoring of cells in both 2D and 3D cell cultures. Developments in electrical monitoring of cell culture have led to novel approaches, proposed by adapting fundamentals of 2D electrical techniques to 3D to obtain high spatiotemporal systems. In this review, we classified these approaches into five main groups: (i) 3D impedance measurement approach (ii) electrical impedance tomography, (iii) 3D microelectrode array approach, (iv) 3D nanoelectronics scaffold approach, and (v) microphysiometry. We also defined the challenges in the adaptation of electrical monitoring techniques to 3D cultures and explained possible solutions in terms of specific applications and technical point of views, including methods particular to our group. In conclusion, 3D electrical monitoring in cell cultures is considerably challenging but highly accelerated recently by significant advances of microfabrication technology, bioengineering, and material science. Novel approaches reviewed here have a lot of potential and offer opportunities for further developments to find solutions, fit to serve the (bio)medical needs.

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来源期刊
Organs-on-a-chip
Organs-on-a-chip Analytical Chemistry, Biochemistry, Genetics and Molecular Biology (General), Cell Biology, Pharmacology, Toxicology and Pharmaceutics (General)
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