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Mesenchymal Stem Cell Differentiation Induced by Lyophilized PRP During Early Osteogenesis
Marcel Rodrigues Ferreira1, Geórgia da Silva Feltran1, Anderson Moreira Gomes1
1Lab. of Bioassays and Cellular Dynamics, Department of Chemistry and Biochemistry, Institute of Biosciences, UNESP: São Paulo State University, Botucatu, São Paulo, Brazil.
Cell Biology International
|November 13, 2025
Summary
Platelet-rich plasma (PRP) promotes mesenchymal stem cell (MSC) proliferation and adhesion but shows weaker osteogenic commitment compared to osteoinductive medium. Further research is needed to optimize PRP for bone healing applications.
Area of Science:
- Biomaterials Science
- Stem Cell Biology
- Regenerative Medicine
Background:
- Platelet-rich plasma (PRP) is rich in bioactive factors that influence tissue repair.
- The specific effects of PRP on osteoblastic commitment in human mesenchymal stem cells (hMSCs) are not fully understood.
Purpose of the Study:
- To investigate the transcriptional response of hMSCs to PRP and lyophilized PRP (lyPRP).
- To compare the osteoinductive potential of PRP/lyPRP with osteoinductive medium (OM).
Main Methods:
- hMSCs were exposed to PRP, lyPRP, or OM for 24 hours or 7 days.
- A 48-gene panel assessing differentiation, adhesion, cell cycle, and signaling pathways was quantified.
- Two-way ANOVA, principal component analysis (PCA), and correlation networks were used for analysis.
Main Results:
- PRP and lyPRP upregulated proliferation, viability, and adhesion-related genes (e.g., cyclins/CDKs, SRC-axis).
- Canonical osteogenic markers (RUNX2, SP7, ALPL) were less induced by PRP/lyPRP compared to OM.
- PCA and network analysis revealed distinct signaling patterns between PRP/lyPRP and OM treatments over time.
Conclusions:
- PRP and lyPRP promote early proliferative and matrix-interaction states in hMSCs.
- PRP/lyPRP exhibit lower osteoinductive transcriptional pressure compared to OM.
- Optimizing PRP formulation, dosage, and timing is crucial for enhancing osteogenic differentiation for therapeutic goals.
Keywords:
gene expression analysismesenchymal stem cellsosteoblastic differentiationplatelet‐rich plasmatherapeutic applications
