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Platelet function under flow can be assessed and simulated hemostatic resuscitation can be modeled using a microfluidic device, which has applications in trauma and transfusion medicine.
Microfluidics incorporate physiologically relevant substrates and flows that mimic the vasculature and are, therefore, a valuable tool for studying aspects of thrombosis and hemostasis. At high-shear environments simulating arterial flow, a microfluidic assay facilitates the study of platelet function, as platelet-rich thrombi form in a localized stenotic region of a flow channel. Utilizing devices that allow for small sample volume can additionally aid in evaluating platelet function under flow from volume-limited patient samples or animal models. Studying trauma patient samples or samples following platelet product transfusion may aid in directing therapeutic strategies for patient populations in which platelet function is critical. Effects of platelet inhibition via pharmacological agents can also be studied in this model. The objective of this protocol is to establish a microfluidic platform that incorporates physiologic flow, biological surfaces, and relevant hemostatic mechanisms to assess platelet function with implications for the study of trauma induced coagulopathy and transfusion medicine.
Trauma is a leading global cause of death and disability. Severe injury is frequently complicated by a unique, endogenous disturbance of hemostasis and thrombosis, termed trauma-induced coagulopathy (TIC)1. Platelets play a critical role in TIC, and they have been described as having both adaptive and maladaptive functions2. The mechanisms of platelet dysfunction after injury remain unclear, and there is a critical need to better understand the cellular response to guide the development of improved resuscitation and therapy. An additional vexing problem regarding platelet function after injury is the uncertainty of the r....
All research was performed in compliance with institutional guidelines. Approval from the University of Pittsburgh Human Research Protection Office was obtained and informed consent from healthy human volunteers was obtained.
1. Microfluidic device preparation
Microfluidic experiments following the use of this method should show platelet-rich thrombi formation in the region of stenosis of the flow channel (Figure 1). Figure 1A illustrates representative results where functional platelets formed a thrombus in the stenotic region of the channel to block blood flow through the channel. Mean fluorescence intensity (MFI) curves of kinetic images taken for the duration of the experiment illustrate a lag, growth, and plateau.......
The above protocol has some critical steps to ensure the reliability and reproducibility of experiments. First, fluorescent antibodies should be carefully considered. The antibodies used to detect platelets in the sample should not block the function of the glycoprotein Ib (GPIb) platelet receptor. Lot matching, whenever possible between experiments, is also critical to ensure the reproducibility of the fluorescent signal. Another critical step in this protocol is using sterile consumables and solutions and filtered samp.......
The authors acknowledge and thank all blood donors who participated, as well as the Trauma and Transfusion Medicine Research Lab phlebotomists and the UPMC Montefiore Clinical and Translational Research Center for assistance in collections. SMS is supported by K25HL161401. MDN is supported by 1R01HL166944-01A1.
....Name | Company | Catalog Number | Comments |
Equipments | |||
Axio Observer | Zeiss | 491917-0001-000 | |
Bel-Art Space Saver Vacuum Desiccators | Fisher Scientific | 08-594-15A | |
Fisherbrand Isotemp Digital Hotplate Stirrer | Fisher Scientific | FB30786161 | |
Nutating Mixer | Fischer Scientific | 88-861-043 | |
OHAUS Scout Balance Scale | Uline | H-5852 | |
Oven | Fisher Scientific | 15-103-0520 | |
Plasma cleaner | Harrick | PDC-32G (115V) | |
Syringe Pump (PHD ULTRA CP, I/W PROGRAMMABLE) | Harvard Apparatus | 883015 | |
Zen 3.4 | Zeiss | Blue edition | Software |
Material | |||
1/16 inch ID - Barbed Elbow Connectors | Qosina | 11691 | |
10 mL syringe | Fischer Scientific | 14-955-459 | |
2-Hydroxypropyl-β-cyclodextrin | Cayman Chemicals | 16169 | 30% Dissolved in Phosphate buffered saline |
40-micron filters | Fischer Scientific | NC1469671 | |
CD41 antibody | Novus Biologicals | Â NB100-2614 | 1:600 Ratio in Whole Blood |
Chrono-Par Collagen Reagent | Chrono Log Corporation | 385 | 1:5 Ratio in 0.9% Saline |
Electron Microscopy Sciences Miltex Biopsy Punch with Plunger, 3.0 mm | Fisher Scientific | NC0856599 | |
Eppendorf Snap-Cap Microcentrifuge SafeLock Tubes, 1.5 mL | Fisher Scientific | 05-402-25 | |
Essendant 121oz. Clorox Germicidal Bleach | Fischer Scientific | 50371500 | |
Ethanol | Fisher Scientific | 07-678-005 | 70% |
Falcon Safety Dust Off DPSXLRCP Compressed Gas | Supra | 1381978 | |
Human TruStain | Biolegend | 422302 | 1:600 Ratio in Whole Blood |
LevGo smartSpatula Disposable Polypropylene Spatula | Fisher Scientific | 18-001-017 | |
Microscope Slides | Fisher Scientific | 12-550-A3 | |
Phosphate buffered saline | Gibco | 10010-023 | |
Safety Scalpel | Fisher Scientific | 22-079-718 | |
Saline | Millipore | 567442 | 0.90% |
Sartorius Polystyrene Weighing Boats | Fisher Scientific | 13-735-744 | |
Superslip Cover Slips - Superslip No. 1.5 | Fisher Scientific | 12-541-055 | |
SYLGARD 184 Silicone Elastomer Kit | Fisher Scientific | NC9285739 | Polydimethylsiloxane (PDMS) |
Ticagrelor | Cayman Chemicals | 15425 | |
Tygon PVC Clear Tubing 1/16" ID, 1/8" OD, 50 ft length | McMaster-Carr | 6516T11 | |
Ultra-Machinable 360 Brass Bar | McMaster-Carr | 8954K721 | For master mold fabrication |
Vacutainers | BD | 363083 | |
World Precision Instrument Reusable Biopsy Punch, 1.5mm | Fisher Scientific | NC1215626 |
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