Single-Cell Tumbling Enables High-Resolution Size Profiling of Retinal Stem Cells

被引:11
|
作者
Gomis, Surath [1 ]
Labib, Mahmoud [2 ]
Coles, Brenda L. K. [3 ]
van der Kooy, Derek [3 ]
Sargent, Edward H. [1 ]
Kelley, Shana O. [2 ]
机构
[1] Univ Toronto, Dept Elect & Comp Engn, Toronto, ON M5S 3G4, Canada
[2] Univ Toronto, Dept Pharmaceut Sci, Toronto, ON M5S 3M2, Canada
[3] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院;
关键词
retinal stem cells; microfluidics; deterministic lateral displacement; ciliary epithelium; label-free; size-sorting; cell tumbling; DETERMINISTIC LATERAL DISPLACEMENT; ADULT MAMMALIAN EYE; MICROFLUIDIC SYSTEMS; PARTICLE SEPARATION; WHOLE-BLOOD; RARE CELL;
D O I
10.1021/acsami.8b10513
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Retinal stem cells (RSCs) are promising candidates for patient-derived cell therapy to repair damage to the eye; however, RSCs are rare in retinal samples and lack validated markers, making cell sorting a significant challenge. Here we report a high-resolution deterministic lateral displacement microfluidic device that profiles RSCs in distinct size populations. Only by developing a chip that promotes cell tumbling do we limit cell deformation through apertured channels and thereby increase the size-sorting resolution of the device. We systematically explore a spectrum of microstructures, including optimized notched pillars, to study and then rationally promote cell tumbling. We find that RSCs exhibit larger diameters than most ciliary epithelial cells, an insight into RSC morphology that allows enrichment from biological samples.
引用
收藏
页码:34811 / 34816
页数:6
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