TY - JOUR
T1 - Technical advance
T2 - Microfluidic assay for precise measurements of mouse, rat, and human neutrophil chemotaxis in whole-blood droplets
AU - Jones, Caroline N.
AU - Hoang, Anh N.
AU - Martel, Joseph M.
AU - Dimisko, Laurie
AU - Mikkola, Amy
AU - Inoue, Yoshitaka
AU - Kuriyama, Naohide
AU - Yamada, Marina
AU - Hamza, Bashar
AU - Kaneki, Masao
AU - Warren, H. Shaw
AU - Brown, Diane E.
AU - Irimia, Daniel
N1 - Publisher Copyright:
© Society for Leukocyte Biology.
PY - 2016/7
Y1 - 2016/7
N2 - Animal models of human disease differ in innate immune responses to stress, pathogens, or injury. Precise neutrophil phenotype measurements could facilitate interspecies comparisons. However, such phenotype comparisons could not be performed accurately with the use of current assays, as they require the separation of neutrophils from blood using species-specific protocols, and they introduce distinct artifacts. Here, we report a microfluidic technology that enables robust characterization of neutrophil migratory phenotypes in a manner independent of the donor species and performed directly in a droplet of whole blood. The assay relies on the particular ability of neutrophils to deform actively during chemotaxis through microscale channels that block the advance of other blood cells. Neutrophil migration is measured directly in blood, in the presence of other blood cells and serum factors. Our measurements reveal important differences among migration counts, velocity, and directionality among neutrophils from 2 common mouse strains, rats, and humans.
AB - Animal models of human disease differ in innate immune responses to stress, pathogens, or injury. Precise neutrophil phenotype measurements could facilitate interspecies comparisons. However, such phenotype comparisons could not be performed accurately with the use of current assays, as they require the separation of neutrophils from blood using species-specific protocols, and they introduce distinct artifacts. Here, we report a microfluidic technology that enables robust characterization of neutrophil migratory phenotypes in a manner independent of the donor species and performed directly in a droplet of whole blood. The assay relies on the particular ability of neutrophils to deform actively during chemotaxis through microscale channels that block the advance of other blood cells. Neutrophil migration is measured directly in blood, in the presence of other blood cells and serum factors. Our measurements reveal important differences among migration counts, velocity, and directionality among neutrophils from 2 common mouse strains, rats, and humans.
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U2 - 10.1189/jlb.5TA0715-310RR
DO - 10.1189/jlb.5TA0715-310RR
M3 - Article
C2 - 26819316
AN - SCOPUS:84976558039
SN - 0741-5400
VL - 100
SP - 241
EP - 247
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
IS - 1
ER -