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Measurement of Cellular Chemotaxis with ECIS/Taxis
Published on: April 1, 2012
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Cell chemotaxis on paper for diagnostics
David I Walsh1, Mark L Lalli1, Juliette M Kassas1
1†Department of Bioengineering, ‡Department of Chemical Engineering, §Department of Biology, ∥Barnett Institute of Chemical and Biological Analysis, Northeastern University, Boston, Massachusetts, United States.
Analytical Chemistry
|May 5, 2015
Summary
This study introduces a low-cost paperfluidic device for rapid chemokine gradient generation, enabling faster cell migration studies. The platform facilitates directed T-cell migration, paving the way for point-of-care diagnostic tools.
Area of Science:
- Biomedical Engineering
- Cell Biology
- Microfluidics
Background:
- Traditional microfluidic chemotaxis platforms require specialized equipment and long incubation times.
- Existing systems are not readily adaptable for rapid diagnostics or point-of-care applications.
Purpose of the Study:
- To develop a low-cost, rapidly assembled paperfluidic device for generating stable chemokine gradients.
- To enable short-term cell migration studies and assess directed cell movement.
- To establish a foundational technology for future microfluidic diagnostic platforms.
Main Methods:
- A novel paperfluidic device was designed for rapid (<1 second) chemokine gradient generation.
- The device produces a quasi-stable gradient for at least 20 minutes.
- Human pan-T cells were utilized to demonstrate proof-of-concept cell migration in response to the gradient.
Main Results:
- The paperfluidic device successfully generated a sharp chemokine gradient.
- Human pan-T cells exhibited significant directed migration towards the chemokine gradient (p ≪ 0.01).
- Cell migration response was observed within a short 20-minute timeframe.
Conclusions:
- The developed paperfluidic device offers a low-cost, efficient alternative for creating chemokine gradients.
- This technology significantly reduces the time required for cell migration studies.
- The platform represents a foundational step towards developing microfluidic chemotaxis systems for point-of-care diagnostics.
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