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一种高通量微流控单细胞筛选平台,能够进行选择性细胞提取。

A high-throughput microfluidic single-cell screening platform capable of selective cell extraction.

机构信息

Department of Electrical and Computer Engineering, Texas A&M University, College Station, Texas 77843, USA.

出版信息

Lab Chip. 2015 Jun 7;15(11):2467-75. doi: 10.1039/c4lc01316f. Epub 2015 May 5.

DOI:10.1039/c4lc01316f
PMID:25939721
Abstract

Microfluidic devices and lab-on-a-chip technologies have been extensively used in high-throughput single-cell analysis applications using their capability to precisely manipulate cells as well as their microenvironment. Although significant technological advances have been made in single-cell capture, culture, and analysis techniques, most microfluidic systems cannot selectively retrieve samples off-chip for additional examinations. Being able to retrieve target cells of interest from large arrays of single-cell culture compartments is especially critical in achieving high-throughput single-cell screening applications, such as a mutant library screening. We present a high-throughput microfluidic single-cell screening platform capable of investigating cell properties, such as growth and biomolecule production, followed by selective extraction of particular cells showing desired traits to off-chip reservoirs for sampling or further analysis. The developed platform consists of 1024 single-cell trapping/culturing sites, where opening and closing of each trap can be individually controlled with a microfluidic OR logic gate. By opening only a specific site out of the 1024 trapping sites and applying backflow, particular cells of interest could be selectively released and collected off-chip. Using a unicellular microalga Chlamydomonas reinhardtii, single-cell capture and selective cell extraction capabilities of the developed platform were successfully demonstrated. The growth profile and intracellular lipid accumulation of the cells were also analyzed inside the platform, where 6-8 hours of doubling time and on-chip stained lipid bodies were successfully identified, demonstrating the compatibility of the system for cell culture and fluorescent tagging assays.

摘要

微流控装置和芯片实验室技术已经被广泛应用于高通量单细胞分析应用中,其能够精确操作细胞及其微环境。尽管在单细胞捕获、培养和分析技术方面取得了重大技术进展,但大多数微流控系统无法从芯片上选择性地获取样品进行进一步检查。能够从大量单细胞培养隔室中选择性地获取目标细胞,对于实现高通量单细胞筛选应用(如突变体文库筛选)至关重要。我们提出了一种高通量微流控单细胞筛选平台,能够研究细胞特性,如生长和生物分子的产生,然后选择性地提取表现出所需特性的特定细胞,以便将其从芯片上的特定位置取出进行采样或进一步分析。所开发的平台由 1024 个单细胞捕获/培养位点组成,其中每个陷阱的打开和关闭都可以通过微流控或逻辑门单独控制。通过仅打开 1024 个捕获位点中的一个特定位点,并施加回流,特定的感兴趣的细胞可以被选择性地释放并从芯片上取走。利用单细胞微藻莱茵衣藻(Chlamydomonas reinhardtii),成功地展示了所开发平台的单细胞捕获和选择性细胞提取能力。还在平台内部分析了细胞的生长情况和细胞内脂质积累情况,成功识别了 6-8 小时的倍增时间和芯片上染色的脂滴,证明了该系统在细胞培养和荧光标记测定方面的兼容性。

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