Babic Julien, Griscom Laurent, Cramer Jeremy, Coudreuse Damien
SyntheCell team, Institute of Genetics and Development of Rennes, CNRS UMR 6290, 2 avenue du Pr. Léon Bernard, 35043, Rennes, France.
Cherry Biotech, 6 rue Gurvan, 35000, Rennes, France.
BMC Cell Biol. 2018 Jun 20;19(1):8. doi: 10.1186/s12860-018-0158-z.
Real-time monitoring of cellular responses to dynamic changes in their environment or to specific treatments has become central to cell biology. However, when coupled to live-cell imaging, such strategies are difficult to implement with precision and high time resolution, and the simultaneous alteration of multiple parameters is a major challenge. Recently, microfluidics has provided powerful solutions for such analyses, bringing an unprecedented level of control over the conditions and the medium in which cells under microscopic observation are grown. However, such technologies have remained under-exploited, largely as a result of the complexity associated with microfabrication procedures.
In this study, we have developed simple but powerful microfluidic devices dedicated to live-cell imaging. These microsystems take advantage of a robust elastomer that is readily available to researchers and that presents excellent bonding properties, in particular to microscopy-grade glass coverslips. Importantly, the chips are easy-to-build without sophisticated equipment, and they are compatible with the integration of complex, customized fluidic networks as well as with the multiplexing of independent assays on a single device. We show that the chips are re-usable, a significant advantage for the popularization of microfluidics in cell biology. Moreover, we demonstrate that they allow for the dynamic, accurate and simultaneous control of multiple parameters of the cellular environment.
While they do not possess all the features of the microdevices that are built using complex and costly procedures, the simplicity and versatility of the chips that we have developed make them an attractive alternative for a range of applications. The emergence of such devices, which can be fabricated and used by any laboratory, will provide the possibility for a larger number of research teams to take full advantage of these new methods for investigating cell biology.
实时监测细胞对其环境动态变化或特定处理的反应已成为细胞生物学的核心内容。然而,当与活细胞成像结合时,此类策略难以精确且高时间分辨率地实施,同时改变多个参数是一项重大挑战。最近,微流控技术为这类分析提供了强大的解决方案,在显微镜观察下细胞生长的条件和培养基方面带来了前所未有的控制水平。然而,此类技术尚未得到充分利用,这主要是由于与微制造工艺相关的复杂性。
在本研究中,我们开发了用于活细胞成像的简单但功能强大的微流控装置。这些微系统利用了一种对研究人员来说容易获得的坚固弹性体,该弹性体具有出色的粘结性能,特别是与显微镜级玻璃盖玻片的粘结性能。重要的是,这些芯片无需复杂设备即可轻松构建,并且它们与复杂的定制流体网络的集成以及在单个设备上进行独立检测的多重化兼容。我们表明这些芯片可重复使用,这对于微流控技术在细胞生物学中的普及是一个显著优势。此外,我们证明它们能够对细胞环境的多个参数进行动态、准确和同时的控制。
虽然我们开发的芯片不具备使用复杂且昂贵程序制造的微型设备的所有特征,但它们的简单性和多功能性使其成为一系列应用的有吸引力的替代方案。这种任何实验室都可以制造和使用的设备的出现,将为更多研究团队充分利用这些研究细胞生物学的新方法提供可能性。