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      The Effect of Platelet-Rich Plasma Formulations and Blood Products on Human Synoviocytes : Implications for Intra-articular Injury and Therapy

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          Abstract

          Background

          The effect of platelet-rich plasma (PRP) on chondrocytes has been studied in cell and tissue culture, but considerably less attention has been given to the effect of PRP on synoviocytes. Fibroblast-like synoviocytes (FLS) compose 80% of the normal human synovium and produce cytokines and matrix metalloproteinases that can mediate cartilage catabolism.

          Purpose

          To compare the effects of leukocyte-rich PRP (LR-PRP), leukocyte-poor PRP (LP-PRP), red blood cell (RBC) concentrate, and platelet-poor plasma (PPP) on human FLS to determine whether leukocyte and erythrocyte concentrations of PRP formulations differentially affect the production of inflammatory mediators.

          Study Design

          Controlled laboratory study.

          Methods

          Peripheral blood was obtained from 4 donors and processed to create LR-PRP, LP-PRP, RBCs, and PPP. Human synoviocytes were cultured for 96 hours with the respective experimental conditions using standard laboratory conditions. Cell viability and inflammatory mediator production were then evaluated.

          Results

          Treatment with LR-PRP resulted in significantly greater synoviocyte death (4.9% ± 3.1%) compared with LP-PRP (0.72% ± 0.70%; P = .035), phosphate-buffered saline (PBS) (0.39% ± 0.27%; P = .018), and PPP (0.26% ± 0.30%; P = .013). Synoviocytes treated with RBC concentrate demonstrated significantly greater cell death (12.5% ± 6.9%) compared with PBS ( P < .001), PPP ( P < .001), LP-PRP ( P < .001), and LR-PRP (4.9% ± 3.1%; P < .001). Interleukin (IL)–1β content was significantly higher in cultures treated with LR-PRP (1.53 ± 0.86 pg/mL) compared with those treated with PBS (0.22 ± 0.295 pg/mL; P < .001), PPP (0.11 ± 0.179 pg/mL; P < .001), and RBCs (0.64 ± 0.58 pg/mL; P = .001). IL-6 content was also higher with LR-PRP (32,097.82 ± 22,844.300 pg/mL) treatment in all other groups ( P <.001). Tumor necrosis factor–α levels were greatest in LP-PRP (9.97 ± 3.110 pg/mL), and this was significantly greater compared with all other culture conditions ( P < .001). Interferon-γ levels were greatest in RBCs (64.34 ± 22.987 pg/mL) and significantly greater than all other culture conditions ( P <.001).

          Conclusion

          Treatment of synovial cells with LR-PRP and RBCs resulted in significant cell death and proinflammatory mediator production.

          Clinical Relevance

          Clinicians should consider using leukocyte-poor, RBC-free formulations of PRP when administering intra-articularly.

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          Author and article information

          Journal
          7609541
          467
          Am J Sports Med
          Am J Sports Med
          The American journal of sports medicine
          0363-5465
          1552-3365
          23 February 2018
          14 March 2014
          May 2014
          01 April 2018
          : 42
          : 5
          : 1204-1210
          Affiliations
          Stanford University, Palo Alto, California, USA
          Author notes
          []Address correspondence to Jason L. Dragoo, MD, Department of Orthopaedic Surgery, Stanford University, 450 Broadway Street, Pavilion C, 4th Floor, Redwood City, CA 94063-6342, USA ( jdragoo@ 123456stanford.edu )
          [*]

          Department of Orthopaedic Surgery, Stanford University, Palo Alto, California, USA.

          [†]

          School of Medicine, University of California–San Francisco, San Francisco, California, USA.

          Article
          PMC5878923 PMC5878923 5878923 nihpa945521
          10.1177/0363546514525593
          5878923
          24634448
          210e9cf3-10b3-49a4-9fae-55147f9dbbd6

          For reprints and permission queries, please visit SAGE’s Web site at http://www.sagepub.com/journalsPermissions.nav

          History
          Categories
          Article

          platelet-rich plasma,synoviocytes,osteoarthritis,inflammation

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