Analysing calcium signalling of cells under high shear flows using discontinuous dielectrophoresis

被引:18
作者
Soffe, Rebecca [1 ]
Baratchi, Sara [2 ,3 ]
Tang, Shi-Yang [1 ]
Nasabi, Mahyar [1 ]
McIntyre, Peter [2 ,3 ]
Mitchell, Arnan [1 ]
Khoshmanesh, Khashayar [1 ]
机构
[1] RMIT Univ, Sch Elect & Comp Engn, Melbourne, Vic, Australia
[2] RMIT Univ, Hlth Innovat Res Inst, Melbourne, Vic, Australia
[3] RMIT Univ, Sch Med Sci, Melbourne, Vic, Australia
基金
澳大利亚研究理事会;
关键词
INTEGRIN FUNCTION; SEPARATION; TRPV4; MANIPULATION; ENRICHMENT; PLATFORMS; ADHESION; CHANNEL; CULTURE; PROTEIN;
D O I
10.1038/srep11973
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
Immobilisation of cells is an important feature of many cellular assays, as it enables the physical/chemical stimulation of cells; whilst, monitoring cellular processes using microscopic techniques. Current approaches for immobilising cells, however, are hampered by time-consuming processes, the need for specific antibodies or coatings, and adverse effects on cell integrity. Here, we present a dielectrophoresis-based approach for the robust immobilisation of cells, and analysis of their responses under high shear flows. This approach is quick and label-free, and more importantly, minimises the adverse effects of electric field on the cell integrity, by activating the field for a short duration of 120 s, just long enough to immobilise the cells, after which cell culture media (such as HEPES) is flushed through the platform. In optimal conditions, at least 90% of the cells remained stably immobilised, when exposed to a shear stress of 63 dyn/cm(2). This approach was used to examine the shear-induced calcium signalling of HEK-293 cells expressing a mechanosensitive ion channel, transient receptor potential vaniloid type 4 (TRPV4), when exposed to the full physiological range of shear stress.
引用
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页数:13
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