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Measurement of cell migration in response to an evolving radial chemokine gradient triggered by a microvalve.

TitleMeasurement of cell migration in response to an evolving radial chemokine gradient triggered by a microvalve.
Publication TypeJournal Article
Year of Publication2006
AuthorsFrevert, CW, Boggy, G, Keenan, TM, Folch, A
JournalLab Chip
Volume6
Issue7
Pagination849-56
Date Published2006 Jul
ISSN1473-0197
KeywordsChemotaxis, Leukocyte, Dose-Response Relationship, Drug, Humans, Interleukin-8, Microfluidic Analytical Techniques, Microscopy, Fluorescence, Neutrophils
Abstract

We describe a novel chemotaxis assay based on the microvalve-actuated release of a chemoattractant from a cell-free microchamber into a cell-containing microchamber. The microvalve chemotaxis device (microVCD) was placed on the stage of a conventional inverted microscope to obtain time-lapse micrographs of neutrophils migrating in a radially-symmetric evolving gradient of the chemotactic factor CXCL8/Interleukin-8. A fluorescent tracer was added to the CXCL8 solution to visualize the evolution of the gradient profile, so that at each time point the cell positions could be assigned CXCL8 concentration values. Tracking of individual neutrophils for 90 minutes showed that (a) the neutrophil migratory response is, on average, radially directed towards the CXCL8 source; (b) significant non-radial displacements occur frequently; and (c) there is considerable heterogeneity in the migration speeds and directions amongst the neutrophil population. A custom-made imaging analysis tool was used to extract measurements of migratory behavior such as speed, velocity along the gradient's radial axis, and the cosine of the turning angle as a function of CXCL8 concentration. The microVCD can be easily adapted to study the migratory behavior of cultured cells other than neutrophils.

DOI10.1039/b515560f
Alternate JournalLab Chip
PubMed ID16804588
Grant ListEB003307 / EB / NIBIB NIH HHS / United States
R21 RR030249-02 / RR / NCRR NIH HHS / United States
R33 EB003307 / EB / NIBIB NIH HHS / United States