Tissue Eng Regen Med.  2017 Oct;14(5):567-577. 10.1007/s13770-017-0062-1.

Platelet Rich Plasma and Culture Configuration Affect the Matrix Forming Phenotype of Bone Marrow Stromal Cells

Affiliations
  • 1Stem Cells and Cell Therapy Laboratory, BioCruces Health Research Institute, Cruces University Hospital, 48903 Barakaldo, Spain.
  • 2Regenerative Medicine Laboratory, BioCruces Health Research Institute, Cruces University Hospital, Pza Cruces 12, 48903 Barakaldo, Spain. iandia2010@hotmail.com
  • 3Centro Tecnolo´gico IK4-Ideko, 20870 Elgoibar, Spain.

Abstract

We aim to examine the influence of platelet rich plasma (PRP) and spatial cues in cartilage/bone matrix forming proteins, and to evaluate the mitotic and chemotactic potential of PRP on human mesenchymal stem cells (hMSCs). Directed cell migration towards PRP gradients was assessed in chemotactic chambers, and recorded by time-lapse microscopy. hMSCs cultured in three-dimensional (3D) scaffolds were visualized by scanning electron microscopy; Hoechst dye was used to confirm cell confluence in 3D-constructs and monolayers before experimental treatment. MSCs were treated with 10% PRP lysate or 10% PRP lysate supplemented with TGF-β-based differentiation medium. The expression of cartilage (COL2A1, Sox9, ACAN, COMP), and bone (COL1A1, VEGF, COL10A1, Runx2) fundamental genes was assessed by real time PCR in monolayers and 3D-constructs. PRP had mitotic (p <.001), and chemotactic effect on hMSCs, Ralyleigh test p = 1.02E - 10. Two and three-week exposure of MSCs to PRP secretome in 3Dconstructs or monolayers decreased Sox9 expression (p <0.001 and p = 0.050) and COL2A1, (p = 0.011 and p = 0.019). MSCs in monolayers exposed to PRP showed increased ACAN (p = 0.050) and COMP (p <0.001). Adding TGF-β-based differentiation medium to PRP increased COMP, and COL2A1 expression at gene and protein level, but merely in 3D-constructs, p <0.001. TGF-β addition to monolayers reduced Sox9 (p <0.001), aggrecan (p = 0.004), and VEGF (p = 0.004). Cells exposed to PRP showed no changes in hypertrophy associated genes in either monolayers or 3Dconstructs. Our study suggests hMSCs have high-degree of plasticity having the potential to change their matrix-forming phenotype when exposed to PRP and according to spatial configuration.

Keyword

Joint repair; Human mesenchymal stem cells (hMSCs); Platelet rich plasma (PRP); 3D-cultures

MeSH Terms

Aggrecans
Blood Platelets*
Bone Marrow*
Cartilage
Cell Movement
Cues
Humans
Hypertrophy
Mesenchymal Stromal Cells*
Microscopy
Microscopy, Electron, Scanning
Phenotype*
Plastics
Platelet-Rich Plasma*
Real-Time Polymerase Chain Reaction
Vascular Endothelial Growth Factor A
Aggrecans
Plastics
Vascular Endothelial Growth Factor A
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