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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Platelet metabolism is of interest, particularly as it relates to the role of platelet hyper- and hypoactivity in bleeding and thrombotic disorders. Isolating platelets from plasma is necessary for some metabolic assays; presented here is a method for isolating of intracellular metabolites from washed platelets.

Abstract

Platelets are blood cells that play an integral role in hemostasis and the innate immune response. Platelet hyper- and hypoactivity have been implicated in metabolic disorders, increasing risk for both thrombosis and bleeding. Platelet activation and metabolism are tightly linked, with the numerous methods to measure the former but relatively few for the latter. To study platelet metabolism without the interference of other blood cells and plasma components, platelets must be isolated, a process that is not trivial because of platelets shear sensitivity and ability to irreversibly activate. Presented here is a protocol for platelet isolation (washing) that produces quiescent platelets that are sensitive to stimulation by platelet agonists. Successive centrifugation steps are used with the addition of platelet inhibitors to isolate platelets from whole blood and resuspend them in a controlled, isosmotic buffer. This method reproducibly produces 30%–40% recovery of platelets from whole blood with low activation as measured by markers of granule secretion and integrin activity. Platelet count and fuel concentration can be precisely controlled to allow the user to probe a variety of metabolic situations.

Introduction

Platelets are small (2–4 µm diameter), anucleate cells that play an important role in hemostasis, the tightly regulated process of clot formation1. While vital for vascular integrity, platelets are also implicated in adverse health events. Platelets are involved in deep vein thrombosis (DVT) and arterial thrombosis (AT), which are clots that occlude blood vessels, leading to diminished blood supply locally, or, if pieces of the clot break off (embolize), they can block blood supply to the lungs, heart, or brain2,3,4,

Protocol

The study received Institutional Review Board approval from the University of Colorado Anschutz Medical Campus. Written consent was obtained from all study participants. Participants reported they did not consume alcohol for the previous 48 h or non-steroidal anti-inflammatory drugs (NSAIDs) for the previous ten days. This project is supported by the National Heart, Lung, and Blood Institute of the National Institutes of Health under award number R61HL141794.

1. Blood collection.......

Representative Results

Representative results in Figure 2 represent 6 different blood donors, including 3 males and 3 females. The platelet yield relative to whole blood is shown in Figure 2A. Final platelet recovery was an average of 52% ± 3% (standard deviation, n=6). Final platelet count compared to white blood cell contamination was measured using an automated hematology analyzer. White blood cell counts were less than 0.1% of total cells (Figure 2B

Discussion

Platelets are very sensitive to their environment, including shear stress and presence of agonists38,39. This makes platelets challenging to handle and isolate, making the use of inhibitors and wide bore pipettes crucial40. Proper storage and preparation of PGI2 is vital, as failing to prepare PGI2 in basic PBS will result in rapid degradation of PGI241. To minimize the risk of shear.......

Acknowledgements

The authors would like to acknowledge Dr. Emily Janus-Bell and Clarisse Mouriaux from the lab of Dr. Pierre Mangin and Katrina Bark from Dr. Jorge DiPaola’s lab for their guidance and advice.

....

Materials

NameCompanyCatalog NumberComments
0.22 µM filter Spin-X tubesMillapore-SigmaCLS8160Reagent prep
19 G x 3/4" needleMcKesson Corporation448406Phlebotomy
21 G 1.5 inch needle with luer lockAmazonB0C39PJD23Reagent prep
96 well plate, half areaGreiner Bio-One675101Flow cytometry
ACD-A vaccutainers Fisher Scientific364606Phlebotomy
AdapterMcKesson Corporation609Phlebotomy
Alcohol swabVWR15648-916Phlebotomy
Apyrase from potatoesSigmaA6410-100UNReagent prep
CD42a Monoclonal AntibodyThermo Fisher Scientific48-0428-42Flow cytometry
Chilled microcentrifuge ThermoFisher Scientific75002441Quenching
D-GlucoseSigmaG7021Reagent prep
FITC Anti-Fibrinogen antibodyAbcam4217Flow cytometry
Flow cytometerBeckman Coulter82922828Flow cytometry
GauzeVWR76049-110Phlebotomy
GlycerolSigma AldrichG5516Reagent prep
HEPESSigma AldrichH4034Reagent prep
Human alpha-thrombinProlytixHCT-0020Flow cytometry
KClSigma AldrichP9333Reagent prep
KH2PO4Sigma AldrichP5655Reagent prep
MgCl2SigmaM8266Reagent prep
Microcentrifuge tubesVWR87003-292General
Na2HPO4SigmaS3264Reagent prep
NaClSigma AldrichS7653Reagent prep
NaHCO3Sigma AldrichS5761Reagent prep
Narrow bore transfer pipetteVWR16001-176Platelet washing
Paraformaldehyde solution, 4% in PBSSanta Cruz Biotechnologysc-281692Flow cytometry
PECy5 Mouse Anti-Human CD62PBD Pharmingen551142Flow cytometry
Plate coverThermo Fisher ScientificAB0626Flow cytometry
Polypropylene 15 mL conical tubesVWR89039-658Reagent prep
Polypropylene 50 mL conical tubesVWR352070Platelet washing
Prostaglandin I2 (sodium salt)Cayman Chemical18220Reagent prep
SKC Inc. C-Chip Disposable HemocytometersFisher Scientific22-600-100Cell counting
SyringeBD Pharmingen14-823-41Reagent prep
TourniquetVWR76235-371Phlebotomy
Vacutainer needle holderBD364815Phlebotomy
VortexerVWR102091-234Reagent prep
Water bathThermo Fisher ScientificTSGP02Platelet washing
Wide bore transfer pipetteVWR76285-362Platelet washing

References

  1. Versteeg, H. H., Heemskerk, J. W., Levi, M., Reitsma, P. H. New fundamentals in hemostasis. Physiol Rev. 93 (1), 327-358 (2013).
  2. Webera, M., et al. Enhanced platelet aggregation with trap-6 and collagen....

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