4.7 Article

Osteogenesis Enhancement with 3D Printed Gene-Activated Sodium Alginate Scaffolds

Journal

GELS
Volume 9, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/gels9040315

Keywords

osteogenesis; bone regeneration; sodium alginate; plasmid DNA; gene-activated hydrogel scaffolds; 3D printing

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Natural and synthetic hydrogel scaffolds are commonly used in tissue engineering, and encapsulating DNA-encoding growth factors into these scaffolds is a promising approach for delivering genes to the site of bone defects. In this study, 3D printed sodium alginate hydrogel scaffolds were impregnated with model EGFP and therapeutic BMP-2 plasmids to assess their osteogenic properties. The expression levels of MSC osteogenic differentiation markers and bone formation in vivo were evaluated. The results showed that the SA/pBMP-2 scaffolds had a significant increase in new bone volume compared to the SA/pEGFP ones.
Natural and synthetic hydrogel scaffolds containing bioactive components are increasingly used in solving various tissue engineering problems. The encapsulation of DNA-encoding osteogenic growth factors with transfecting agents (e.g., polyplexes) into such scaffold structures is one of the promising approaches to delivering the corresponding genes to the area of the bone defect to be replaced, providing the prolonged expression of the required proteins. Herein, a comparative assessment of both in vitro and in vivo osteogenic properties of 3D printed sodium alginate (SA) hydrogel scaffolds impregnated with model EGFP and therapeutic BMP-2 plasmids was demonstrated for the first time. The expression levels of mesenchymal stem cell (MSC) osteogenic differentiation markers Runx2, Alpl, and Bglap were evaluated by real-time PCR. Osteogenesis in vivo was studied on a model of a critical-sized cranial defect in Wistar rats using micro-CT and histomorphology. The incorporation of polyplexes comprising pEGFP and pBMP-2 plasmids into the SA solution followed by 3D cryoprinting does not affect their transfecting ability compared to the initial compounds. Histomorphometry and micro-CT analysis 8 weeks after scaffold implantation manifested a significant (up to 46%) increase in new bone volume formation for the SA/pBMP-2 scaffolds compared to the SA/pEGFP ones.

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