Microgel Single-Cell Culture Arrays on a Microfluidic Chip for Selective Expansion and Recovery of Colorectal Cancer Stem Cells

被引:26
作者
Lin, Dongguo [1 ,2 ,3 ]
Chen, Xiao [1 ]
Liu, Yang [1 ]
Lin, Zhun [1 ]
Luo, Yanzhang [2 ]
Fu, Mingpeng [2 ]
Yang, Na [2 ]
Liu, Dayu [1 ,2 ,3 ]
Cao, Jie [1 ,4 ]
机构
[1] South China Univ Technol, Sch Med, Guangzhou 510006, Peoples R China
[2] South China Univ Technol, Guangzhou Peoples Hosp 1, Dept Lab Med, Guangzhou 510180, Peoples R China
[3] Guangdong Engn Technol Res Ctr Microfluid Chip Me, Guangzhou 510180, Peoples R China
[4] South China Univ Technol, Affiliated Hosp 2, Guangzhou 510180, Peoples R China
基金
中国博士后科学基金;
关键词
ALGINATE; IDENTIFICATION; MICROENVIRONMENT; GENERATION; ASSAY;
D O I
10.1021/acs.analchem.1c02335
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Cancer stem cells (CSCs) are rare and lack definite biomarkers, necessitating new methods for a robust expansion. Here, we developed a microfluidic single-cell culture (SCC) approach for expanding and recovering colorectal CSCs from both cell lines and tumor tissues. By incorporating alginate hydrogels with droplet microfluidics, a high-density microgel array can be formed on a microfluidic chip that allows for single-cell encapsulation and nonadhesive culture. The SCC approach takes advantage of the self-renewal property of stem cells, as only the CSCs can survive in the SCC and form tumorspheres. Consecutive imaging confirmed the formation of single-cell-derived tumorspheres, mainly from a population of small-sized cells. Through on-chip decapsulation of the alginate microgel, similar to 6000 live cells can be recovered in a single run, which is sufficient for most biological assays. The recovered cells were verified to have the genetic and phenotypic characteristics of CSCs. Furthermore, multiple CSC-specific targets were identified by comparing the transcriptomics of the CSCs with the primary cancer cells. To summarize, the microgel SCC array offers a label-free approach to obtain sufficient quantities of CSCs and thus is potentially useful for understanding cancer biology and developing personalized CSC-targeting therapies.
引用
收藏
页码:12628 / 12638
页数:11
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