A subscription to JoVE is required to view this content. Sign in or start your free trial.
This protocol generates bioparticle microarrays that provide spatially controlled neutrophil swarming. It provides easy access to the mediators that neutrophils release during migration and allows for quantitative imaging analysis.
Neutrophil swarming is a cooperative process by which neutrophils seal off a site of infection and promote tissue reorganization. Swarming has classically been studied in vivo in animal models showing characteristic patterns of cell migration. However, in vivo models have several limitations, including intercellular mediators that are difficult to access and analyze, as well as the inability to directly analyze human neutrophils. Because of these limitations, there is a need for an in vitro platform that studies swarming with human neutrophils and provides easy access to the molecular signals generated during swarming. Here, a multistep microstamping process is used to generate a bioparticle microarray that stimulates swarming by mimicking an in vivo infection. The bioparticle microarray induces neutrophils to swarm in a controlled and stable manner. On the microarray, neutrophils increase in speed and form stable swarms around bioparticle clusters. Additionally, supernatant generated by the neutrophils was analyzed and 16 proteins were discovered to have been differentially expressed over the course of swarming. This in vitro swarming platform facilitates direct analysis of neutrophil migration and protein release in a reproducible, spatially controlled manner.
Neutrophils, the most abundant white blood cell in the bloodstream1, are gaining attention as potential diagnostic and therapeutic targets2,3 because they may be involved in a variety of medical conditions including gout4, sepsis3, trauma5,6, cancer1,7,8, and various autoimmune diseases5,9. Neutrophil swarming is a multistage, tigh....
The authors acknowledge the healthy volunteers who kindly donated their blood. Blood specimens were obtained after informed volunteer consent according to institutional review board (IRB) protocol #2018H0268 reviewed by the Biomedical Sciences Committee at The Ohio State University.
1. Microfabrication of bioparticle microarray
When neutrophils are added to the bioparticle microarray, neutrophils that contact the bioparticle clusters become activated and initiate the swarming response. The bioparticle microarray was validated using time-lapse fluorescent microscopy to track neutrophil migration toward the bioparticle clusters (Video S1). The migration of individual neutrophil nuclei is tracked as they migrate toward the bioparticle cluster. When neutrophils reach the bioparticle cluster, their nuclei overlap with other nuclei i.......
We developed a microstamping platform to generate uniform arrays of bioparticles to stimulate in vitro neutrophil swarming. The in vitro nature of our platform allows us to circumvent the complications that arise with in vivo swarming experiments, namely the poor ability to analyze mediators released by swarming neutrophils5. Additionally, in vivo models are typically performed in rodents11,12,13,
This work was supported by funding from the William G. Lowrie Department of Chemical and Biomolecular Engineering and the Comprehensive Cancer Center at The Ohio State University. Data presented in this report came from images processed using Imaris x64 (ver. 9.3.0 Bitplane) available at the Campus Microscopy and Imaging Facility, The Ohio State University. This facility is supported in part by grant P30 CA016058, National Cancer Institute, Bethesda, MD.
....Name | Company | Catalog Number | Comments |
"The Big Easy" EasySep Magnet | STEMCELL Technologies | 18001 | Magnet to use with neutrophil isolation kit |
Cell Incubator | Okolab | 777057437 / 77057343 | Okolab cage incubator for temperature and CO2 control |
EasySep Human Neutrophil Isolation Kit | STEMCELL Technologies | 17957 | Kit for immunomagnetic negative selection of human neutrophils |
Eclipse Ti2 | Nikon Instruments | MEA54010 / MEF55037 | Inverted research microscope |
Escherichia coli (K-12 strain) BioParticles Texas Red conjugate | Invitrogen | E2863 | Bioparticle powder, dissolve in water prior to addition to Zetag® array |
Harris Uni-Core 8-mm biopsy punch | Sigma Aldrich | Z708925 | To cut PDMS stamps |
HetaSep | STEMCELL Technologies | 7906 | Erythrocyte aggregation agent for separating buffy coat from red blood cells in fresh human blood |
Hoechst 33342 | Life Technologies | H3570 | Nucleus fluorescent stain |
Human L1000 Array | Raybiotech Inc. | AAH-BLG-1000-4 | High density array to detect 1000 human proteins |
Human Serum Albumin (HSA) | Sigma Aldrich | A5843 | Low endotoxin HSA, to prepare 2 % solutions in IMDM for isolated neutrophils |
Iscove's Modified Dulbeccos' Medium (IMDM) | Thermo Fisher Scientific | 12440053 | To resuspend isolated neutrophils |
K2-EDTA tubes | Thermo Fisher Scientific | 02-657-32 | Tubes for blood collection |
Low Reflective Chrome Photomask | Front Range Photomask | N/A | Dimensions 5" x 5" x 0.09" (L x W x D) |
Microarray Scanner | Perkin Elmer | ASCNGX00 | Fluorescence reader of protein patterned microdomains |
Microscopy Image Analsysis Software - Imaris | Bitplane | 9.3.0 | Software for automatic cell tracking analysis |
NiS Elements Advanced Research Software Package | Nikon Instruments | MQS31100 | Software for automatic live cell imaging and swarm size calculation |
Poly-L-lysine fluorescein isothiocyanate (PLL-FITC) | Sigma Aldrich | P3069-10MG | 30,000 - 70,000 MW PLL labeled with FITC, used to fluorescently label CP solution |
SecureSeal 8-well Imaging Spacer | Grace Bio-Labs | 654008 | 8-well, 9-mm diameter, adhesive imaging spacer |
Silicon Wafer | University Wafer | 590 | Silicon 100 mm N/P (100) 0- 100 ohm-cm 500 μm SSP test |
Spin Coater | Laurell | WS-650MZ-23NPPB | Used to spincoat a 40-µm layer of photoresist onto silicon wafer |
SU-8 2025 | MicroChem | 2025 | Negative photoresist to make silicon master wafer |
SU-8 Developer | MicroChem | Y020100 | Photoresist developer. Remove non-crosslinked SU-8 2025 from silicon wafer |
Sylgard 184 (polydimethylsiloxane, PDMS) | Dow | 1673921 | 2-part silicone elastomer kit for making microstamps and PDMS wells |
UV Exposure Masking System | Kloé | UV-KUB 2 | Used to crosslink photoresist on silicon wafer through chrome mask with UV light |
Water | Thermo Fisher Scientific | A1287303 | High quality water to dilute bioparticles |
Zetag 8185 | BASF | 8185 | Cationic polyelectrolyte (CP), powder, Copolymer of acrylamide and quaternized cationic monomer, forms "inking solution" for microstamping when dissolved in water |
Zymosan A S. cerevisiae BioParticles Texas Red conjugate | Invitrogen | Z2843 | Bioparticle powder, dissolve in water prior to addition to Zetag array |
This article has been published
Video Coming Soon
ABOUT JoVE
Copyright © 2024 MyJoVE Corporation. All rights reserved