Automated single-cell motility analysis on a chip using lensfree microscopy

被引:66
作者
Pushkarsky, Ivan [1 ]
Lyb, Yunbo [2 ]
Weaver, Westbrook [1 ]
Su, Ting-Wei [2 ]
Mudanyali, Onur [2 ]
Ozcan, Aydogan [1 ,2 ,3 ]
Di Carlo, Dino [1 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Elect Engn, Los Angeles, CA 90024 USA
[3] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
BLOOD ANALYSIS; MOVEMENT; TRACKING; RIGIDITY;
D O I
10.1038/srep04717
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Quantitative cell motility studies are necessary for understanding biophysical processes, developing models for cell locomotion and for drug discovery. Such studies are typically performed by controlling environmental conditions around a lens-based microscope, requiring costly instruments while still remaining limited in field-of-view. Here we present a compact cell monitoring platform utilizing a wide-field (24 mm(2)) lensless holographic microscope that enables automated single-cell tracking of large populations that is compatible with a standard laboratory incubator. We used this platform to track NIH 3T3 cells on polyacrylamide gels over 20 hrs. We report that, over an order of magnitude of stiffness values, collagen IV surfaces lead to enhanced motility compared to fibronectin, in agreement with biological uses of these structural proteins. The increased throughput associated with lensfree on-chip imaging enables higher statistical significance in observed cell behavior and may facilitate rapid screening of drugs and genes that affect cell motility.
引用
收藏
页数:8
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