Abstract

Platelet-rich plasma (PRP) is a widely used autologous treatment for tendon injuries in clinics. Platelets (PLTs) are a major source of high mobility group box1 (HMGB1) that is gaining attention as a chemoattractant that can recruit stem cells to the wound area to enhance healing of injured tissues; however, the contribution of PLT HMGB1 in wounded tendon healing remains unexplored. This study investigated the effect of PLT HMGB1 within PRP on tendon healing using PLT HMGB1 knockout (KO) and GFP mice. A window defect was created in the patellar tendons of both groups of mice, and wounds were treated with either saline, PRP isolated from PLT HMGB1-KO mice, or PRP isolated from GFP mice. Seven days post-treatment, animals were sacrificed and analyzed by gross inspection, histology, and immunostaining for characteristic signs of tendon healing and repair. Our results showed that in comparison to mice treated with PRP from PLT HMGB1-KO mice, wounds treated with PRP from GFP mice healed faster and exhibited a better organization in tendon structure. Mice treated with PRP from PLT HMGB1-KO mice produced tendon tissue with large premature wound areas and low cell densities. However, wounds of PLT HMGB1-KO mice showed better healing with PRP from HMGB1-KO mice compared to saline treatment. Moreover, wounds treated with PRP from GFP mice had increased extracellular HMGB1, decreased CD68, increased stem cell markers CD146 and CD73, and increased collagen III protein expression levels compared to those treated with PRP from PLT HMGB1-KO mice. Thus, PLT HMGB1 within PRP plays an important role in tendon wound healing by decreasing inflammation, increasing local HMGB1 levels, and recruiting stem cells to the wound area in the tendon. Our findings also suggest that the efficacy of PRP treatment for tendon injuries in clinics may depend on PLT HMGB1 within PRP preparations.

Highlights

  • Tendon injuries to the Achilles and patellar tendons are prevalent in both occupational and athletics populations

  • In GFP mice, treatment with GFP-platelet-rich plasma (PRP) significantly decreased positively stained CD68 cells (Fig 5K and 5L) compared to the same group treated with PRP from KO mice (Fig 5I and 5J). These results suggest that ablation of PLT high mobility group box1 (HMGB1) in PRP results in significant levels of CD68+ M1 macrophages in treated tendon tissues, while M1 cells are greatly reduced in tendons treated with normal PRP treatments

  • This study investigated the effect of platelet-derived HMGB1 in PRP on wounded tendon healing using a transgenic mouse line with a specific platelet HMGB1 ablation

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Summary

Introduction

Tendon injuries to the Achilles and patellar tendons are prevalent in both occupational and athletics populations. Overall, healing of injured tendons is slow and yields an inferior quality of tendon tissue that is prone to re-injury. Many therapeutic approaches including injection of autologous platelet-rich plasma (PRP) have been devised to manage tendon injuries [1,2]. Several studies have reported that PRP can effectively treat tendon injuries [3,4,5], whereas others have shown the opposite with no improvement in pain or tendon function after PRP treatment [6,7,8]. Further investigation into the role of platelets (PLTs) in tendon wound healing is essential to understand the PLT action mechanism in PRP and improve the efficacy of PRP in the treatment of tendon injuries

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