Magnetic levitation of single cells

被引:169
|
作者
Durmus, Naside Gozde [1 ,2 ]
Tekin, Cumhur [3 ]
Guven, Sinan [3 ]
Sridhar, Kaushik [3 ]
Yildiz, Ahu Arslan [3 ]
Calibasi, Gizem [3 ]
Ghiran, Ionita [4 ]
Davis, Ronald W. [1 ,2 ,5 ]
Steinmetz, Lars M. [2 ,5 ]
Demirci, Utkan [3 ]
机构
[1] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94304 USA
[2] Stanford Univ, Stanford Genome Technol Ctr, Stanford, CA 94304 USA
[3] Stanford Univ, Sch Med, Canary Ctr Stanford Canc Early Detect, Dept Radiol, Stanford, CA 94304 USA
[4] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02115 USA
[5] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94304 USA
基金
美国国家科学基金会;
关键词
magnetic levitation; single cells; real-time monitoring; cell densitometry; cancer; ANTIBIOTIC-RESISTANT BIOFILMS; IRON-OXIDE NANOPARTICLES; CELLULAR HETEROGENEITY; BUOYANT DENSITY; CANCER; VOLUME; FRACTIONATION; APOPTOSIS; CULTURES; YEAST;
D O I
10.1073/pnas.1509250112
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
Several cellular events cause permanent or transient changes in inherent magnetic and density properties of cells. Characterizing these changes in cell populations is crucial to understand cellular heterogeneity in cancer, immune response, infectious diseases, drug resistance, and evolution. Although magnetic levitation has previously been used for macroscale objects, its use in life sciences has been hindered by the inability to levitate microscale objects and by the toxicity of metal salts previously applied for levitation. Here, we use magnetic levitation principles for biological characterization and monitoring of cells and cellular events. We demonstrate that each cell type (i.e., cancer, blood, bacteria, and yeast) has a characteristic levitation profile, which we distinguish at an unprecedented resolution of 1 x 10(-4) g.mL(-1). We have identified unique differences in levitation and density blueprints between breast, esophageal, colorectal, and nonsmall cell lung cancer cell lines, as well as heterogeneity within these seemingly homogenous cell populations. Furthermore, we demonstrate that changes in cellular density and levitation profiles can be monitored in real time at single-cell resolution, allowing quantification of heterogeneous temporal responses of each cell to environmental stressors. These data establish density as a powerful biomarker for investigating living systems and their responses. Thereby, our method enables rapid, density-based imaging and profiling of single cells with intriguing applications, such as label-free identification and monitoring of heterogeneous biological changes under various physiological conditions, including antibiotic or cancer treatment in personalized medicine.
引用
收藏
页码:E3661 / E3668
页数:8
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