R. Uchiyama (Isehara, JP)

Tokai University School of Medicine orthopaedic

Presenter Of 1 Presentation

Poster Growth factors, PRP and Cytokines

P204 - Changes in Platelet Activation Through the Preparation and Freeze-thawing of Platelet Rich Plasma

Presentation Topic
Growth factors, PRP and Cytokines
Date
13.04.2022
Lecture Time
09:30 - 09:30
Room
Exhibition Foyer
Session Name
7.3 - Poster Viewing / Coffee Break / Exhibition
Session Type
Poster Session
Disclosure
No Significant Commercial Relationship

Abstract

Purpose

Osteoarthritis of the knee (OAK) is a chronic degenerative disease accompanied by damage to the articular cartilage, and no current treatment can completely reverse OAK. Recently, joint treatment with platelet-rich plasma (PRP), an autologous blood product generated by centrifuging whole blood and concentrating platelets, has attracted attention as a point-of-care treatment. PRPs used in clinical practice are usually administered to the affected area immediately after preparation, but PRPs used in research is often cryopreserved. However, platelets are known to become activated by stimuli such as freezing or centrifugation. In this study, we compared PRPs prepared with two different kits to investigate the effects of PRP preparation, and freezing and thawing on platelet activation.

Methods and Materials

PRPs were purified from 60 ml of peripheral blood of OAK patients (n=14, 64.0±10.3 years) using JMS Cell-Aid P-type kit (group J) or Zimmer Biomet APS kit (group Z). Surplus PRPs were frozen at -80°C. Using flow cytometry, the expression of CD62P, a marker for activated platelets, was analyzed in peripheral blood, freshly prepared PRP, and frozen-thawed PRP.

Results

The average CD62P positive rates for platelets in peripheral blood (10.5% in group J and 17.6% in group Z) were not significantly different. The platelet activation rates increased significantly in fresh PRP (15.6% in group J and 26.5% in group Z) and were significantly different between the two groups. The platelet activation rates in frozen-thawed PRP (53.5% in group J and 84.3% in group Z) further increased significantly and were significantly different between the two groups.

Conclusion

Platelets are known to release their contained humoral factors when activated. The content of humoral factors may be different in PRPs with different platelet activation rates, leading to possibly different treatment effects. In the future, we will verify this effect on target cells.

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Presenter Of 1 Presentation

Growth factors, PRP and Cytokines

P204 - Changes in Platelet Activation Through the Preparation and Freeze-thawing of Platelet Rich Plasma

Abstract

Purpose

Osteoarthritis of the knee (OAK) is a chronic degenerative disease accompanied by damage to the articular cartilage, and no current treatment can completely reverse OAK. Recently, joint treatment with platelet-rich plasma (PRP), an autologous blood product generated by centrifuging whole blood and concentrating platelets, has attracted attention as a point-of-care treatment. PRPs used in clinical practice are usually administered to the affected area immediately after preparation, but PRPs used in research is often cryopreserved. However, platelets are known to become activated by stimuli such as freezing or centrifugation. In this study, we compared PRPs prepared with two different kits to investigate the effects of PRP preparation, and freezing and thawing on platelet activation.

Methods and Materials

PRPs were purified from 60 ml of peripheral blood of OAK patients (n=14, 64.0±10.3 years) using JMS Cell-Aid P-type kit (group J) or Zimmer Biomet APS kit (group Z). Surplus PRPs were frozen at -80°C. Using flow cytometry, the expression of CD62P, a marker for activated platelets, was analyzed in peripheral blood, freshly prepared PRP, and frozen-thawed PRP.

Results

The average CD62P positive rates for platelets in peripheral blood (10.5% in group J and 17.6% in group Z) were not significantly different. The platelet activation rates increased significantly in fresh PRP (15.6% in group J and 26.5% in group Z) and were significantly different between the two groups. The platelet activation rates in frozen-thawed PRP (53.5% in group J and 84.3% in group Z) further increased significantly and were significantly different between the two groups.

Conclusion

Platelets are known to release their contained humoral factors when activated. The content of humoral factors may be different in PRPs with different platelet activation rates, leading to possibly different treatment effects. In the future, we will verify this effect on target cells.

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