journal article·2018-10-17

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

Surath Gomis, Mahmoud Labib, Brenda L. K. Coles, Derek van der Kooy, Edward H. Sargent, Shana O. Kelley

ACS Applied Materials & Interfaces· Volume 10· Issue 41
Publisher page

Abstract

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.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Microfluidic and Bio-sensing Technologies · 3D Printing in Biomedical Research · Electrowetting and Microfluidic Technologies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Electrical and Computer Engineering, University of Toronto, Toronto, Ontario M5S 3G4, Canada

Department of Pharmaceutical Sciences, University of Toronto, Toronto, Ontario M5S 3M2, Canada

Department of Molecular Genetics, University of Toronto, Toronto, Ontario M5S 1A8, Canada

Funding

Government of Canada · Canada First Research Excellence Fund (CFREF)

References (27)

Show source-provided references
1. 10.1136/bjophthalmol-2013-30403310.1136/bjophthalmol-2013-304033 ↗
2. 10.1016/S0140-6736(12)60028-210.1016/S0140-6736(12)60028-2 ↗
3. 10.1038/nbt.411410.1038/nbt.4114 ↗
4. 10.1016/j.ophtha.2018.04.03710.1016/j.ophtha.2018.04.037 ↗
5. 10.1126/science.287.5460.203210.1126/science.287.5460.2032 ↗
6. 10.1006/bbrc.2000.247310.1006/bbrc.2000.2473 ↗
7. 10.1242/bio.201202710.1242/bio.2012027 ↗
8. 10.1039/C5LC01173F10.1039/C5LC01173F ↗
9. 10.1038/ncomms642710.1038/ncomms6427 ↗
10. 10.1039/C5LC00314H10.1039/C5LC00314H ↗
11. 10.1089/ten.tea.2013.046810.1089/ten.tea.2013.0468 ↗
12. 10.1007/s00216-010-3721-910.1007/s00216-010-3721-9 ↗
13. 10.1039/C4LC01246A10.1039/C4LC01246A ↗
14. 10.1126/science.109456710.1126/science.1094567 ↗
15. 10.1039/b912547g10.1039/b912547g ↗
16. 10.1021/ac061542n10.1021/ac061542n ↗
17. 10.1016/j.snb.2017.01.11310.1016/j.snb.2017.01.113 ↗
18. 10.1002/elps.20070060710.1002/elps.200700607 ↗
19. 10.1039/C4LC00939H10.1039/C4LC00939H ↗
20. Davis, J. A. Microfluidic Separation of Blood Components through Deterministic Lateral Displacement. Ph.D. Thesis, Princeton University, Princeton, NJ, 2008.
21. 10.1007/s10404-010-0635-y10.1007/s10404-010-0635-y ↗
22. 10.1038/ncomms265310.1038/ncomms2653 ↗
23. 10.1038/s41598-017-01150-310.1038/s41598-017-01150-3 ↗
24. 10.1080/0361092890883012710.1080/03610928908830127 ↗
25. 10.1039/C6AY00443A10.1039/C6AY00443A ↗
26. 10.1039/C4LC00578C10.1039/C4LC00578C ↗
27. 10.1063/1.493717110.1063/1.4937171 ↗