Purification of Platelets from Mouse Blood

Summary

Here, mouse blood was collected in the presence of an anti-coagulant. The platelets were purified by iohexol gradient medium using low speed centrifugation. The platelets were activated with thrombin to investigate if they were viable. The quality of the purified platelets was analyzed by flow cytometry and microscopy.

Abstract

Platelets are purified from whole blood to study their functional properties, which should be free from red blood cells (RBC), white blood cells (WBC), and plasma proteins. We describe here purification of platelets from mouse blood using three-fold more iohexol gradient medium relative to blood sample volume and centrifugation in a swinging bucket rotor at 400 x g for 20 min at 20 °C. The recovery/yield of the purified platelets were 18.2-38.5%, and the purified platelets were in a resting state, which did not contain any significant number of RBC and WBC. The purified platelets treated with thrombin showed up to 93% activation, indicating their viability. We confirmed that the purified platelets are sufficiently pure using flow cytometric and microscopic evaluation. These platelets can be used for gene expression, activation, granule release, aggregation, and adhesion assays. This method can be used for purification of platelets from the blood of other species as well.

Introduction

Platelets are a component of blood that functions as an initiator of blood clotting in response to damage in the blood vessel. They gather at the site of injury to plug the vessel wall¹. Platelets are anucleate fragments of cytoplasm derived from the megakaryocytes of the bone marrow under the influence of thrombopoietin and enter the circulation². They are considered as metabolically active and capable of sensing extracellular environment by activating intracellular signaling cascades that result in platelet spreading, aggregation, and hemostatic plug formation^1,3. Besides hemostasis/thrombosis and wound healing⁴, platelets play an important role in host inflammatory responses, angiogenesis, and metastatis^3,5,6,7,8.

Platelets are purified from blood to study their biochemical and physiological properties, which should be free from other blood components. Since red blood cells (RBC) and white blood cells (WBC) contain significantly more RNA and proteins than platelets^9,10, the presence of even a small number of these cells can interfere with transcriptomic and proteomic analyses of RNA and proteins derived from platelets. We found that purified platelets activated with thrombin bind antibody such as anti-GPIIb/IIIa (JON/A) and anti-P-selectin more efficiently than whole blood platelets.

Since platelets are fragile, it is important to treat the samples as mildly as possible. If the platelets are activated, they release their granule contents and ultimately degrade. Therefore, to keep the platelets’ functional properties intact, it is important to maintain platelet quiescence during isolation. Several protocols have described isolation of platelets from human, dog, rat, and non-human primate by various methods^1,10,11,12. Some of the methods require multiple steps such as collection of platelet-rich plasma by centrifugation, filtration by separation column, negative selection of platelets with RBC- and WBC-specific antibody conjugated to magnetic beads, and so on, which are time-consuming and may degrade platelets and their contents.

Ford and his colleagues described platelet purification from human blood using iohexol medium¹¹. This method uses a similar volume of blood sample and medium during purification. Since humans yield a higher volume of blood, it is relatively easy to purify the platelets.

Iohexol is a universal density gradient inert medium that is freely soluble in water and used in the fractionation of nucleic acids, proteins, polysaccharides, and nucleoproteins^13,14. It has low osmolality and is non-toxic, thus making it an ideal medium for purification of intact living cells¹¹. It is a non-particulate medium; therefore, the distribution of cells in a gradient can be determined using hemocytometer, flow cytometer, or spectrophotometer. It does not interfere with most of the enzymatic or chemical reaction of the cells or cellular fragments after dilution.

The mouse serves as an important animal model for many human diseases^15,16,17,18. There are a few published articles that describe purification of mouse platelets^19,20. However, the mouse yields a relatively smaller volume of blood, which makes it difficult to purify platelets. If the same small volume of gradient medium and blood samples is used, the platelet layer cannot be clearly separated from RBC-WBC layer after centrifugation. In this article, we have described a quick and simple method of mouse platelet purification with three-fold more iohexol gradient medium relative to the blood sample volume and low speed centrifugation. We have also activated the purified platelets with thrombin and investigated their quality with flow cytometry and microscopy.

Protocol

Mouse blood collection should be conducted with appropriate institutional animal care and use committee approval.

NOTE: The platelet purification protocol is described in a flow diagram in Figure 1.

1. Collection of Blood

1. Add 25 µL of 3.2% sodium citrate (pH 7.2) as an anti-coagulant and 0.4 mM of Gly-Pro-Arg-Pro (GPRP) in a polypropylene tube.
2. Collect approximately 200 µL of blood from the C57BL/6 mouse using retro-orbital bleeding.
   NOTE: Blood can be collected from any type of mouse strain regardless of age or gender.
   1. Use 2 mL of isoflurane in any type of chamber to anesthetize the mouse.
      NOTE: Depth of anesthesia is checked by signs of increased respiration and decreased movement. The mouse should not respond to movement of the anesthesia chamber, or to being handled. If the mouse is responsive to movement or handling, then it requires more time to keep in the anesthesia chamber.
   2. 1.2.2 Open either right or left eyelid of the mouse and insert a 7.5 cm (0.12 cm diameter) capillary tube into the vascular plexus of the eye.
   3. Twist the capillary tube one half turn while applying pressure to the capillary tube to break the vessels and initiate blood flow. Hold the animal upside down over the collection vial to be filled by capillary action.
   4. Once the appropriate volume of blood is collected, remove the capillary tube and close the eye by applying mild pressure for 30 s on the eyelid with gauze. Once bleeding is stopped, return the mouse to its cage and monitor for bleeding.
   5. Check eyes for trauma 1-2 days after retro-orbital bleeding. Remove any mouse from the study showing signs of significant trauma to the eye as a result of the procedure and euthanize.
      NOTE: The mouse should not undergo any kind of treatment which can inhibit platelets for at least two weeks before blood collection. The blood sample must be used for platelet purification within one hour of bleeding the mouse.

2. Platelet Purification

NOTE: Platelet purification should be carried out at room temperature to prevent their degradation. Make sure that temperature of the reagents and instruments are between 18 to 22 °C. To prevent platelet degradation, fast pipetting and vigorous shaking should be avoided during the procedure.

1. Add 600 µL of iohexol gradient medium (12% iohexol powder in 0.85% sodium chloride, 5 mM Tricine, pH 7.2)¹¹ into an 1.5 mL tube.
2. Add 200 µL of blood sample slowly down the side of the tube on top of the gradient medium with a wide bore pipette tip so that blood and iohexol medium do not mix (Figure 2A).
3. Centrifuge the sample containing tube at 400 x g for 20 min at 20 °C in a swinging bucket rotor with slow acceleration and deceleration.
4. Collect most of the platelet-rich layer and a small fraction of platelet-poor layer (total 300 to 400 µL) using a wide bore pipette tip without disturbing the RBC and WBC layers (Figure 2B). Transfer the platelet sample to a new tube.
   NOTE: If the platelet count is less in the blood or a smaller volume of blood is used, the platelet-rich layer and platelet-poor layer can be seen as a single layer.
5. Add 1 mL of PBS to the platelet sample, mix by inverting, and centrifuge at 800 x g for 10 min at 20 °C in a swinging bucket rotor. Discard the solution completely and add 200 µL of PBS to resuspend the platelets with mild pipetting.
   NOTE: This step is optional, as it removes the gradient medium and plasma proteins and increases the sensitivity of platelets to agonists such as thrombin. Since different centrifuges have different programs, the slow acceleration/deceleration can be determined by reading the user manual of the centrifuge.
6. Transfer 30 µL of this sample into a new tube to count platelets. The remaining platelets can be used for biochemical and physiological assays such as platelet activation, aggregation, granule release, etc.
7. For RNA or protein extraction, centrifuge the platelet sample at 800 x g for 10 min to pellet the platelets. Discard supernatant completely without disturbing the pellet. Add the desired volume of RNA or protein lysis buffer to lyse the platelets.

3. Counting the Platelets

1. Count the whole blood cells without dilution and purified platelets (diluted 2 to 5-fold with PBS) using an automated cell analyzer. Use 30 to 50 µL samples for counting.
2. Calculate the total number of platelets by multiplying by the volume of the sample.
3. Calculate the percentage of yield/recovery of purified platelets.
4. Count the RBC and WBC in the purified platelet sample (diluted 50 to 100-fold with PBS) with a hemocytometer and microscope.

4. Platelet Activation

1. In a tube, add 1 to 2 million purified platelets in up to 100 µL of staining buffer (PBS with 2% fetal bovine serum, FBS).
2. For multiple number of samples, make a master mix of antibodies with 1 µL (0.5 mg/mL) of the following: PE-Cy7 rat anti-mouse TER 119, PE rat anti-mouse CD45, FITC rat anti-mouse CD41, and APC rat anti-mouse/human CD62P (P-selectin) to detect RBC, WBC, platelets, and activated platelets, respectively. Add the master mix to the tubes for staining the cells. Do not add thrombin.
3. In another tube, add 1 to 2 million of purified platelets in up to 100 µL of staining buffer, and 0.4 mM GPRP peptide. Add thrombin to activate the platelets and stain the cells following step 4.2.
   NOTE: GPRP should be added to the sample before adding thrombin to prevent aggregate or clot formation through platelet activation. Thrombin concentration should be optimized to obtain good activation of platelets. After platelet activation, event counts are decreased during acquisition of samples by flow cytometry.
4. As a positive control, add 1 µL of whole blood in up to 100 µL staining buffer in a tube and 0.4 mM GPRP peptide. Add thrombin to activate platelets. As a negative control, add 1 µL of whole blood in up to 100 µL of staining buffer. Do not add thrombin in negative control sample. Stain the cells following step 4.2.
5. For flow cytometry isotype control, label 5 tubes with unstained, PE-Cy7, PE, FITC, and APC. Add 100 µL of staining buffer, 1 µL of blood, and 1 µL of the respective antibody to the labeled tubes to stain the cells.
6. Incubate samples to stain for 30 min at room temperature in the dark.
7. Wash the samples by adding 1 mL of staining buffer to each tube. Centrifuge at 800 x g for 5 min at room temperature. Discard the staining buffer carefully without dislodging the pellet.
8. Add 300 µL of staining buffer to each tube, mix mildly, and transfer to a FACS tube. Store the stained samples in the dark until analyzed with a flow cytometer.

5. Flow Cytometry Analyses of Platelets

1. Create a new experiment and generate log forward scatter vs log side scatter dot plots and assign gates for Ter119 PE-Cy7 (RBC), CD45 PE (WBC), CD41 FITC (platelets), and CD62P APC (activated platelets) populations according to the gating strategy chosen for the experiment in the FACS DIVA software.
   1. Open the population hierarchy by choosing Show Population Hierarchy under the Populations tab. Edit the population hierarchy by checking the gating strategy and properly renaming the gates.
   2. Open statistics view by choosing Create Statistics View. Edit statistics view according to user preferences by right clicking the statistics view and selecting Edit Statistics View.
   3. Choose a color for each gate that enhances the visual aspect of the layout by double clicking on the box corresponding to the population.
2. In the Cytometer window, click on the Parameters tab and adjust the voltages for parameters to visualize the population of interest on the plots.
3. Adjust voltages for each of the parameters so that the negative population can be distinguished from the positive population. Before recording the samples for the compensation control, check that the single-stained positive controls are on scale (ensure that the positive peaks are visible and not too far to the right).
   NOTE: If the positive peaks are off scale, the voltages should be adjusted to see the positive populations.
4. Record the single-color stained cells for compensation controls (unstained, PE-Cy7, PE, FITC, and APC).
5. If the positive control gates are not set up properly, adjust them by changing voltages.
6. Go to Experiment > Compensation Setup > Calculate Compensation. Choose Apply Only in the resulting window.
7. Switch to the global worksheet by clicking on the toggle button in the top, left of the worksheet window.
8. Load the positive control sample and acquire enough cells to adjust the compensation and the gates.
9. Load the sample again and check that each plot shows the expected cell population based on the fluorochrome stained antibody. Acquire and record 100,000 events for whole blood samples and 10,000 events for purified platelets. Load the samples one by one until acquisition is completed.
10. Analyze the flow cytometry data with the software with appropriate plots and gates (Figure 3)

Results

The summary of platelet purification is described in a flow diagram (Figure 1). Steps include collection of blood from mouse using retro-orbital bleeding in the presence of an anticoagulant, addition of blood sample onto the iohexol gradient medium, centrifugation in a swinging bucket rotor at 400 x g for 20 min at 20 °C. The quality of the purified platelets was evaluated with microscopy and flow cytometry after staining with antibody to detect any contaminating cells and activated...

Discussion

Commonly, platelets are isolated by low-speed centrifugation which yields platelet-rich plasma that contains a significant number of blood cells, cellular debris, and plasma proteins which can interfere with the biochemical and physiological assays and needs further purification²¹. Therefore, it is important to use a rapid and simple method which can yield pure platelets without major contaminants. The protocol presented here describes the purification of platelets from mouse blood using a gradien...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
APC rat anti-mouse/human CD62P (P-selectin)	Thermoscientific	17-0626-82	Platelets activation marker
Eppendorf tube	Fisher Scientific	14-222-166	Tube for centifuge
FACS DIVA software	BD Biosciences	Non-catalog item	Analysis of platelets and whole blood
FACS tube	Fisher Scientific	352008	Tubes for flow cytomtery
Fetal bovine serum (FBS)	Invitrogen	26140079	Ingredient for staining buffer
FITC rat anti-mouse CD41	BD Biosciences	553848	Platelets marker
Flow cytometer	BD Biosciences	Non-catalog item	Analysis of platelets and whole blood
FlowJo software	FlowJo, Inc.	Non-catalog item	Analysis of platelets and whole blood
Gly-Pro-Arg-Pro (GPRP)	EMD Millipore	03-34-0001	Prevent platelet clot formation
Hematocrit Capillary tube	Fisher Scientific	22-362566	Blood collection capillary tube
Hemavet	Drew Scientific	Non-catalog item	Blood cell analyzer
Hemocytometer	Hausser Scientific	3100	Cell counting chamber
Isoflurane	Baxter	1001936040	Use to Anesthetize mouse
Microscope (Olympus CKX41)	Olympus	Non-catalog item	Cell monitoring and counting
Nycodenz (Histodenz)	Sigma-Aldrich	D2158	Gradient medium
PE rat anti-mouse CD45	BD Biosciences	561087	WBC marker
PE-Cy7 rat anti-mouse TER 119	BD Biosciences	557853	RBC marker
Pipet tips 200 µL, wide-bore	ThermoFisher Scientific	21-236-1A	Transferring blood and platelet samples
Pipet tips 1000 µL, wide-bore	ThermoFisher Scientific	21-236-2C	Transferring blood and platelet samples
Phosphate buffured saline (PBS)	ThermoFisher Scientific	14040-117	Buffer for washing and dilution
Sodium chloride	Sigma-Aldrich	S7653	Physiological saline
Sodium citrate	Fisher Scientific	02-688-26	Anti-coagulant
Staining buffer	In-house	Non-catalog item	Wash and dilution buffer
Steile water	In-house	Non-catalog item	Solvent
Table top centrifuge	ThermoFisher Scientific	75253839/433607	Swinging bucket rotor centrifuge
Thrombin	Enzyme Research Laboratoty	HT 1002a	Platelet activation agonist
Tricine	Sigma-Aldrich	T0377	Buffer for Nycodenz medium