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Effects of Allogeneic Platelet-Rich Plasma PRP on the Healing Process of Sectioned Achilles Tendons of Rats: A Methodological Description
Published on: March 19, 2018
Distinct microRNA signatures in Platelet-Rich Plasma-Derived extracellular vesicles predict healing outcomes in
Yu-Chi Tsai1, Shu-Yu Wu2, Chien-Ju Wu3
1Division of Plastic and Reconstruction Surgery, Department of Surgery, Tri-service General Hospital, National Defense Medical University, Taipei, Taiwan; Burn Center, Department of Surgery and Department of Critical Medicine, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan; Division of Traumatology, Department of Surgery, Tri-Service General Hospital, National Defense Medical University, Taipei, Taiwan.
Background:
Diabetic foot ulcers (DFUs) present a major challenge due to impaired angiogenesis and chronic inflammation. Autologous platelet-rich plasma (PRP) is a widely used therapy, but clinical outcomes remain inconsistent. We hypothesized that the microRNA (miRNA) cargo of platelet-derived extracellular vesicles (PRP-EVs) drives this therapeutic variability.
Methods:
Ten patients with refractory DFUs were enrolled. Autologous PRP-EVs were isolated, and wound healing-associated miRNAs were quantified via qRT-PCR. Clinical wound closure was monitored weekly, with the primary efficacy endpoint assessed at 6 weeks. The biological effects of patient-specific PRP-EVs on keratinocyte migration were evaluated in vitro.
Results:
PRP treatment resulted in significant wound area reduction, achieving an average closure rate of approximately 90% by week 6. However, miRNA expression exhibited substantial heterogeneity. High levels of miR-20a-5p and miR-21-5p in PRP-EVs were significantly associated with delayed clinical healing and impaired keratinocyte migration. Conversely, elevated miR-223-3p correlated with accelerated wound closure.
Conclusion:
The intrinsic miRNA composition of PRP-EVs is a critical determinant of PRP therapeutic efficacy. miR-20a-5p and miR-21-5p serve as negative predictive biomarkers, whereas miR-223-3p indicates a favorable prognosis. Profiling these miRNAs offers a novel approach for PRP quality control and personalized regenerative strategies.
Insights
Platelet-rich plasma extracellular vesicles (PRP-EVs) show variable efficacy for diabetic foot ulcers (DFUs). Specific microRNAs (miRNAs) within PRP-EVs predict healing outcomes, enabling personalized regenerative medicine for DFU treatment.
Area of Science:
- Regenerative Medicine
- Molecular Biology
- Wound Healing Research
Background:
- Diabetic foot ulcers (DFUs) are challenging due to poor healing.
- Platelet-rich plasma (PRP) therapy for DFUs has inconsistent results.
- MicroRNAs (miRNAs) within PRP-derived extracellular vesicles (PRP-EVs) may explain this variability.
Purpose of the Study:
- Investigate the role of miRNA cargo in PRP-EVs on DFU healing.
- Identify specific miRNAs as predictors of therapeutic efficacy.
- Assess the potential for personalized regenerative strategies.
Main Methods:
- Isolated autologous PRP-EVs from 10 DFU patients.
- Quantified wound healing-associated miRNAs using qRT-PCR.
- Monitored clinical wound closure and evaluated keratinocyte migration in vitro.
Main Results:
- PRP treatment achieved ~90% wound closure by 6 weeks.
- Heterogeneous miRNA expression was observed in PRP-EVs.
- High miR-20a-5p and miR-21-5p correlated with poor healing; high miR-223-3p correlated with accelerated healing.
Conclusions:
- PRP-EV miRNA composition critically determines therapeutic efficacy.
- miR-20a-5p and miR-21-5p are negative predictive biomarkers for DFU healing.
- miR-223-3p indicates a favorable prognosis, enabling personalized PRP therapy.
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