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一种用于单细胞谱系追踪的图像引导微流控系统。

An image-guided microfluidic system for single-cell lineage tracking.

机构信息

Institute for Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, ETH Zürich, Zürich, Switzerland.

Laboratory of Biology and Modelling of the Cell, Université de Lyon, Ecole Normale Supérieure de Lyon, CNRS, UMR5239, Université Claude Bernard, Lyon, France.

出版信息

PLoS One. 2023 Aug 1;18(8):e0288655. doi: 10.1371/journal.pone.0288655. eCollection 2023.

DOI:10.1371/journal.pone.0288655
PMID:37527253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10393162/
Abstract

Cell lineage tracking is a long-standing and unresolved problem in biology. Microfluidic technologies have the potential to address this problem, by virtue of their ability to manipulate and process single-cells in a rapid, controllable and efficient manner. Indeed, when coupled with traditional imaging approaches, microfluidic systems allow the experimentalist to follow single-cell divisions over time. Herein, we present a valve-based microfluidic system able to probe the decision-making processes of single-cells, by tracking their lineage over multiple generations. The system operates by trapping single-cells within growth chambers, allowing the trapped cells to grow and divide, isolating sister cells after a user-defined number of divisions and finally extracting them for downstream transcriptome analysis. The platform incorporates multiple cell manipulation operations, image processing-based automation for cell loading and growth monitoring, reagent addition and device washing. To demonstrate the efficacy of the microfluidic workflow, 6C2 (chicken erythroleukemia) and T2EC (primary chicken erythrocytic progenitors) cells are tracked inside the microfluidic device over two generations, with a cell viability rate in excess of 90%. Sister cells are successfully isolated after division and extracted within a 500 nL volume, which was demonstrated to be compatible with downstream single-cell RNA sequencing analysis.

摘要

细胞谱系追踪是生物学中长期存在且未解决的问题。微流控技术具有通过快速、可控和高效的方式操作和处理单细胞的能力,有望解决这个问题。事实上,当与传统成像方法结合使用时,微流控系统允许实验人员实时追踪单细胞的分裂过程。在这里,我们提出了一种基于阀的微流控系统,能够通过追踪多个世代的细胞谱系来探测单细胞的决策过程。该系统通过将单个细胞困在生长室内来操作,允许被困的细胞生长和分裂,在用户定义的分裂次数后分离姐妹细胞,最后提取它们进行下游转录组分析。该平台集成了多个细胞操作,基于图像处理的细胞加载和生长监测自动化,试剂添加和设备清洗。为了证明微流控工作流程的有效性,6C2(鸡红细胞白血病)和 T2EC(原代鸡红细胞祖细胞)在微流控装置内追踪了两代,细胞存活率超过 90%。分裂后成功分离出姐妹细胞,并在 500nL 体积内提取,该体积与下游单细胞 RNA 测序分析兼容。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/cf8f44a31df1/pone.0288655.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/bc1b343b1829/pone.0288655.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/1f7428dc3712/pone.0288655.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/5a564e7e3780/pone.0288655.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/9e5eafab8e5e/pone.0288655.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/cf8f44a31df1/pone.0288655.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/bc1b343b1829/pone.0288655.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/1f7428dc3712/pone.0288655.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/5a564e7e3780/pone.0288655.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/9e5eafab8e5e/pone.0288655.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73c6/10393162/cf8f44a31df1/pone.0288655.g005.jpg

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