• Platelet Preparation

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OUTLINE

In order to avoid platelet activation all manipulations must be performed as quickly and as acurate as possible.Work on ice if possible!

This protocol is based on differential centrifugation that allows to separate platelets from blood cells. Also you can use Robinson procedure (consult the HANDBOOK OF FLOW CYTOMETRY METHODS)

PROTOCOL

1. Bleed animals via the plexus retroorbitalis or the tail vein under ether anesthesia
2. Collect blood into 1,5 eppendorf tubes with ACD (acid-citrate-dextrose; Sigma C-3821) = 1 vol of ACD : 3 vol of blood : 6.6 vol of NaN 3 0,05%-PBS
3. Cetrifuge at 216-220g , 5-7min , 10ѓC 
4. Take & save at 4ѓC PRP (platelet-rich plasma ) 
5. Add 1ml of  either NaN3 0,05%-PBS or BSGC to the remainig eythrocytes and other cells
6. Cetrifuge at 216-220g , 5-7min , 10ѓC
7. Take & save at 4ѓC PRP (platelet-rich plasma )
8. Add 1ml of either NaN3 0,05%-PBS or BSGC to the remainig eythrocytes and other cells
9. Cetrifuge at 216-220g , 5-7min , 10ѓC
10. Take & save at 4ѓC PRP (platelet-rich plasma )
11. Pool saved PRP
12. Cetrifuge at 1613g , 10min , 10ѓC
13. Aspirate supernatant (SN)
14. Resuspend sedimented platelets in either EDTA 1%-NaCl 0.9% or BSGC
    
15. Cetrifuge at 216-220g , 5-7min , 10ѓC
16. Resuspend in in either EDTA 1%-NaCl 0.9% or BSGC. Count platelets
17. Transfer SN into another tube, save at 4ѓC
    

SOLUTIONS

1. ACD = 0.1 mol/L trisodium citrate, 0.11 mol/L dextrose, and 71 mmol/L citric acid monohydrate 
2. ACD pH 4.9 = trisodium citrate dihydrate 22g/L + citric acid monohydrate 8g/L + dextrose 24.5 g/L
3. NaN3 0.05%-PBS (for 500ml) = 100ml PBS(x 5) + 400ml ddH2O + 0.25g NaN 3 pH7.0-7.2 
4. PBS (x5)(phosphate buffer saline x5) (for 5L) = 180g NaCl + 37g Na 2HPO4*2H 2O + 10.75g KH2PO4 + ddHO to 5L
5. EDTA 1%-NaCl 0.9% (for 500ml)= 5g EDTA + 0.9% NaCl to 500ml pH 7.0
   
6. BSGC = 8.6 mM Na2HPO4, 1.6 mM KH2PO4, 0.12 M NaCl, 0.9 mM EDTA, 13.6 mM Na citrate, 11.1 mM glucose, pH 7.3 (Levin et al, 1999)
   

ADDITIONAL INFO

1. it's possible to bleed mice by cardiac puncture under ether anesthesia.
2. it's possible to collect blood into sodium citrate 3.8% ( 0.1 mol/L ) = 1 vol citrate : 9 vol blood : 50 vol buffered saline-glucose-citrate pH7.3 // or heparin 7.5 U/ml   
   
3. RCF = 1.12 x r x (RPM/100) x (RPM/100) where RCF-relative centrifugal force in g  , r -centrifuge radius in mm , RPM-rotations per min in rpm
4. To avoid contamination of PRP with leukocytes and erythrocytes take PRP-upper&middle layers
   

SCHEME


REFERENCES

1. Semple, J.W., Speck, E.R., Cosgrave, D., Lazarus, A.H., Blanchette, V.S. and Freedman, J. (1999). . Blood 93(2): 713-20.
2. Jin, J., Quinton, T.M., Zhang, J., Rittenhouse, S.E. and Kunapuli, S.P. (2002). . Blood 99(1): 193-8.
3. Khetawat, G., Faraday, N., Nealen, M.L., Vijayan, K.V., Bolton, E., Noga, S.J. and Bray, P.F. (2000). . Blood 95(7): 2289-96.

　

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