Leukocyte-Reduced Platelet-Rich Plasma Normalizes Matrix Metabolism in Torn Human Rotator Cuff Tendons

Author:

Cross Jessica A.1,Cole Brian J.2,Spatny Kaylan P.1,Sundman Emily1,Romeo Anthony A.2,Nicholson Greg P.2,Wagner Bettina3,Fortier Lisa A.1

Affiliation:

1. Department of Clinical Sciences, Cornell University, Ithaca, New York, USA

2. Department of Orthopedics, Rush University Medical Center, Chicago, Illinois, USA

3. Department of Population Medicine and Diagnostic Sciences, Cornell University, Ithaca, New York, USA

Abstract

Background: The optimal platelet-rich plasma (PRP) for treatment of supraspinatus tendinopathy has not been determined. Purpose: To evaluate the effect of low- versus high-leukocyte concentrated PRP products on catabolic and anabolic mediators of matrix metabolism in diseased rotator cuff tendons. Study Design: Controlled laboratory study. Methods: Diseased supraspinatus tendons were treated with PRP made by use of 2 commercial systems: Arthrex Autologous Conditioned Plasma Double Syringe System (Llo PRP) and Biomet GPS III Mini Platelet Concentrate System (Lhi PRP). Tendon explants were placed in 6-well plates and cultured in Llo PRP, Lhi PRP, or control media (Dulbecco’s Modified Eagle Medium + 10% fetal bovine serum) for 96 hours. Tendons were processed for hematoxylin-eosin histologic results and were scored with the modified Bonar scale. Group 1 tendons were defined as moderate tendinopathy (Bonar score <3); group 2 tendons were assessed as severely affected (Bonar score = 3). Transforming growth factor β–1 (TGFβ-1), interleukin-1β (IL-1β), interleukin-1 receptor antagonist (IL-1Ra), interleukin-6 (IL-6), interleukin-8 (IL-8), and matrix metalloproteinase–9 (MMP-9) concentrations in PRP media were measured by use of enzyme-linked immunosorbent assay after 96 hours of culture with diseased tendon. Tendon messenger RNA expression of collagen type I ( COL1A1), collagen type III ( COL3A1), cartilage oligomeric matrix protein ( COMP), MMP-9, MMP-13, and IL-1β was measured with real-time quantitative polymerase chain reaction. Results: Leukocytes and platelets were significantly more concentrated in Lhi PRP compared with Llo PRP. Increased IL-1β was present in Lhi PRP after culture with group 1 tendons. IL-6 was increased in Lhi PRP after culture with group 2 tendons. Both TGFβ-1 and MMP-9 were increased in Lhi PRP after culture with either tendon group. In Llo PRP cultures, IL-1Ra:IL-1β in PRP used as media and COL1A1:COL3A1 gene expression were increased for group 1 tendon cultures. Gene expression of MMP-9 and IL-1β was increased in group 2 tendons cultured in Llo PRP. There was no significant difference in the expression of MMP-13 or COMP in either group of tendons cultured in Llo PRP or Lhi PRP. Conclusion: Llo PRP promotes normal collagen matrix synthesis and decreases cytokines associated with matrix degradation and inflammation to a greater extent than does Lhi PRP in moderately degenerative tendons. In severely degenerative tendons, neither PRP preparation enhanced matrix synthesis. Clinical Relevance: Llo PRP may promote healing in moderately degenerative rotator cuff tendons.

Publisher

SAGE Publications

Subject

Physical Therapy, Sports Therapy and Rehabilitation,Orthopedics and Sports Medicine

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