| Literature DB >> 25938457 |
David I Walsh1, Mark L Lalli1, Juliette M Kassas1, Anand R Asthagiri1, Shashi K Murthy1.
Abstract
Microfluidic chemotaxis platforms have historically been utilized to probe phenomena such as neutrophil migration and are beginning to be developed for diagnostic applications; however, current microfluidic chemotaxis systems require specialized engineering equipment such as syringe pumps and long time frames (hours) to develop a chemokine gradient, and cell chemotaxis typically requires multiple additional hours. The paperfluidic device described in this work is a low-cost, sharp (2 mm wide), quasi-stable (at least 20 min) and rapidly generated (<1 s) chemokine gradient system capable of examining cell migration response over short time frames (20 min) that can be easily assembled. A proof-of-concept experiment on human pan-T cells showed significant (p ≪ 0.01) directed migration to the chemokine gradient over the control condition. This new technique for cell migration studies provides a foundational step in designing microfluidic chemotactic platforms for point-of-care diagnostics.Entities:
Mesh:
Year: 2015 PMID: 25938457 DOI: 10.1021/acs.analchem.5b00726
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986