# Perfusion-Limited Efficacy of Platelet-Rich Plasma in Adipose Tissue Grafts

**Authors:** Hanan Jamal Mohamed, Wonwoo Jeong, Jiwon Choi, Min Kyeong Kim, Jonghyeuk Han, Hyun-Wook Kang

PMC · DOI: 10.3390/gels12020185 · Gels · 2026-02-22

## TL;DR

Adding high-dose platelet-rich plasma to fat tissue grafts improves blood flow, survival, and reduces scarring, offering better results for reconstructive surgery.

## Contribution

This study establishes a dose-response relationship for PRP in adipose tissue grafts, identifying optimal concentrations for improved clinical outcomes.

## Key findings

- High-dose PRP increased highly perfused regions in grafts by 8-fold.
- PRP reduced fibrosis by 1.67-fold and improved adipocyte survival by 3.8-fold.
- Graft mass retention was doubled with high-dose PRP compared to native adipose tissue.

## Abstract

Autologous adipose tissue (AT) grafting is often compromised by insufficient early vascularization, leading to ischemia, fibrosis, and inconsistent long-term volume retention. Incorporating platelet-rich plasma (PRP) into AT bioinks offers a clinically accessible means to enhance vascular recruitment, but the in vivo impact of PRP dosage remains unclear. Here, we investigated how PRP concentration, uniformly integrated into a previously reported clinically relevant AT bioink, regulates vascular infiltration, tissue remodeling, and overall graft survival. High-dose PRP markedly improved graft performance, including an 8-fold increase in highly perfused regions, a 3.8-fold enhancement in adipocyte survival, a 1.67-fold reduction in fibrosis, and a 2.51-fold increase in collagen III deposition compared with PRP-free AT grafts. Histological analysis further demonstrated that PRP mitigates the adverse effects of poor perfusion, reducing regional disparities in survival and extracellular matrix (ECM) remodeling. High-dose PRP also maximized graft retention, preserving 103% of graft mass relative to 50.6% in native AT. Together, these results establish a clear in vivo dose–response relationship for PRP-enhanced AT grafts and highlight platelet concentration as a key design parameter for soft-tissue reconstruction. This work provides a translational framework for optimizing PRP-functionalized bioinks to improve clinical outcomes in reconstructive surgery.

## Full-text entities

- **Genes:** Alb (albumin) [NCBI Gene 24186] {aka Alb1, Albza}, Pecam1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 29583] {aka CD31, Pecam}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 83785] {aka VEGF-A, VEGF111, VEGF164, VPF, Vegf}, Plin1 (perilipin 1) [NCBI Gene 25629] {aka PERIA, Plin}, Gatm (glycine amidinotransferase) [NCBI Gene 81660] {aka AT}, F2 (coagulation factor II, thrombin) [NCBI Gene 29251], Tgfb1 (transforming growth factor, beta 1) [NCBI Gene 59086] {aka Tgfb}
- **Diseases:** cytotoxic (MESH:D064420), immunodeficient (MESH:D007153), Fibrosis (MESH:D005355), injury to (MESH:D014947), inflammatory (MESH:D007249), damage (MESH:D020263), ischemia (MESH:D007511), hypoxic (MESH:D002534), AT (MESH:D018205)
- **Chemicals:** streptomycin (MESH:D013307), PCL (MESH:C016240), Picrosirius Red (MESH:C009798), xylene (MESH:D014992), penicillin (MESH:D010406), oxygen (MESH:D010100), ethidium homodimer-1 (MESH:C018533), Alexa Fluor (-), calcein-AM (MESH:C085925), paraffin (MESH:D010232), glucose (MESH:D005947), ethanol (MESH:D000431), DAPI (MESH:C007293), PBS (MESH:D007854), CaCl2 (MESH:D002122), paraformaldehyde (MESH:C003043), isoflurane (MESH:D007530), citrate (MESH:D019343)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940529/full.md

## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940529/full.md

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Source: https://tomesphere.com/paper/PMC12940529