Single-cell migration as studied by scanning electrochemical microscopy

被引:12
|
作者
Ummadi, J. Ganesh [1 ]
Joshi, Vrushali S. [1 ]
Gupta, Priya R. [1 ]
Indra, Arup K. [2 ,3 ,4 ,5 ,6 ]
Koley, Dipankar [1 ]
机构
[1] Oregon State Univ, Dept Chem, Corvallis, OR 97331 USA
[2] Oregon State Univ, Coll Pharm, Dept Pharmaceut Sci, Corvallis, OR 97331 USA
[3] Oregon State Univ, Mol & Cell Biol Program, Corvallis, OR 97331 USA
[4] Oregon Hlth & Sci Univ, Dept Dermatol, Portland, OR 97239 USA
[5] Oregon State Univ, Linus Pauling Inst, Corvallis, OR 97331 USA
[6] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97239 USA
关键词
LIVING CELLS; SECM; ION; MORPHOGENESIS;
D O I
10.1039/c5ay01944c
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Scanning electrochemical microscopy (SECM) was used to study the migration of single live head and neck cancer cells (SCC25). The newly developed graphite paste ultramicroelectrode (UME) showed significantly less fouling in comparison to a 10 mu m Pt-UME and thus could be used to monitor and track the migration pattern of a single cell. We also used SECM probe scan curves to measure the morphology (height and diameter) of a single live cancer cell during cellular migration and determined these dimensions to be 11 +/- 4 mu m and 40 +/- 10 mu m, respectively. The migration study revealed that cells within the same cell line had a heterogeneous migration pattern (migration and stationary) with an estimated migration speed of 8 +/- 3 mu m h(-1). However, serum-starved synchronized cells of the same line were found to have a non-heterogeneous cellular migration pattern with a speed of 9 +/- 3 mu m h(-1). Thus, this non-invasive SECM-based technique could potentially be expanded to other cell lines to study cellular biomechanics for an improved understanding of the structure-function relationship at the level of a single cell.
引用
收藏
页码:8826 / 8831
页数:6
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