Tiemeijer B M, Tel J
Laboratory of Immunoengineering, Department of Biomedical Engineering, TU Eindhoven, Eindhoven, Netherlands.
Institute of Complex Molecular Systems, TU Eindhoven, Eindhoven, Netherlands.
Front Bioeng Biotechnol. 2022 Jun 17;10:891461. doi: 10.3389/fbioe.2022.891461. eCollection 2022.
Single-cell techniques have become more and more incorporated in cell biological research over the past decades. Various approaches have been proposed to isolate, culture, sort, and analyze individual cells to understand cellular heterogeneity, which is at the foundation of every systematic cellular response in the human body. Microfluidics is undoubtedly the most suitable method of manipulating cells, due to its small scale, high degree of control, and gentle nature toward vulnerable cells. More specifically, the technique of microfluidic droplet production has proven to provide reproducible single-cell encapsulation with high throughput. Various in-droplet applications have been explored, ranging from immunoassays, cytotoxicity assays, and single-cell sequencing. All rely on the theoretically unlimited throughput that can be achieved and the monodispersity of each individual droplet. To make these platforms more suitable for adherent cells or to maintain spatial control after de-emulsification, hydrogels can be included during droplet production to obtain "microgels." Over the past years, a multitude of research has focused on the possibilities these can provide. Also, as the technique matures, it is becoming clear that it will result in advantages over conventional droplet approaches. In this review, we provide a comprehensive overview on how various types of hydrogels can be incorporated into different droplet-based approaches and provide novel and more robust analytic and screening applications. We will further focus on a wide range of recently published applications for microgels and how these can be applied in cell biological research at the single- to multicell scale.
在过去几十年中,单细胞技术越来越多地融入细胞生物学研究。人们提出了各种方法来分离、培养、分选和分析单个细胞,以了解细胞异质性,而细胞异质性是人体每一种系统性细胞反应的基础。微流体技术无疑是操纵细胞最合适的方法,因为它规模小、可控性高,且对脆弱细胞性质温和。更具体地说,微流体液滴生成技术已被证明能够以高通量提供可重复的单细胞封装。人们已经探索了各种液滴内应用,包括免疫测定、细胞毒性测定和单细胞测序。所有这些都依赖于理论上可以实现的无限通量以及每个液滴的单分散性。为了使这些平台更适合贴壁细胞,或在破乳后保持空间控制,可以在液滴生成过程中加入水凝胶以获得“微凝胶”。在过去几年中,大量研究集中在这些微凝胶所能提供的可能性上。此外,随着技术的成熟,很明显它将比传统的液滴方法具有优势。在这篇综述中,我们全面概述了各种类型的水凝胶如何融入不同的基于液滴的方法中,并提供新颖且更强大的分析和筛选应用。我们将进一步关注微凝胶最近发表的广泛应用,以及它们如何在单细胞到多细胞尺度的细胞生物学研究中得到应用。