Tracking of lineage mass via quantitative phase imaging and confinement in low refractive index microwells†

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2024-08-20 DOI:10.1039/D4LC00389F
Jingzhou Zhang, Justin Griffin, Koushik Roy, Alexander Hoffmann and Thomas A. Zangle
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引用次数: 0

Abstract

Measurements of cell lineages are central to a variety of fundamental biological questions, ranging from developmental to cancer biology. However, accurate lineage tracing requires nearly perfect cell tracking, which can be challenging due to cell motion during imaging. Here we demonstrate the integration of microfabrication, imaging, and image processing approaches to demonstrate a platform for cell lineage tracing. We use quantitative phase imaging (QPI), a label-free imaging approach that quantifies cell mass. This gives an additional parameter, cell mass, that can be used to improve tracking accuracy. We confine lineages within microwells fabricated to reduce cell adhesion to sidewalls made of a low refractive index polymer. This also allows the microwells themselves to serve as references for QPI, enabling measurement of cell mass even in confluent microwells. We demonstrate application of this approach to immortalized adherent and nonadherent cell lines as well as stimulated primary B cells cultured ex vivo. Overall, our approach enables lineage tracking, or measurement of lineage mass, in a platform that can be customized to varied cell types.

Abstract Image

通过定量相位成像和低折射率微孔中的封闭跟踪系质
细胞系的测量对于从发育生物学到癌症生物学等各种基础生物学问题至关重要。然而,精确的品系追踪需要近乎完美的细胞追踪,而由于成像过程中细胞的运动,这可能具有挑战性。在这里,我们展示了微加工、成像和图像处理方法的整合,从而展示了一个细胞系追踪平台。我们使用定量相位成像(QPI)这种无标记成像方法来量化细胞质量。这就提供了一个额外的参数--细胞质量,可用于提高追踪的准确性。我们将细胞系限制在微孔内,以减少细胞对低折射率聚合物侧壁的粘附。这也使微孔本身成为 QPI 的参照物,即使在汇合微孔中也能测量细胞质量。我们展示了这种方法在永生化粘附和非粘附细胞系以及体内外培养的受刺激原代 B 细胞中的应用。总之,我们的方法可以在一个平台上实现系追踪或系质量测量,该平台可根据不同的细胞类型进行定制。
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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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