3D Printed Gene-Activated Sodium Alginate Hydrogel Scaffolds.
Maria A KhvorostinaAnton V MironovIrina A NedorubovaTatiana Borisovna BukharovaAndrey Vyacheslavovich VasilyevDmitry V GoldshteinVladimir S KomlevVladimir K PopovPublished in: Gels (Basel, Switzerland) (2022)
Gene therapy is one of the most promising approaches in regenerative medicine to restore damaged tissues of various types. However, the ability to control the dose of bioactive molecules in the injection site can be challenging. The combination of genetic constructs, bioresorbable material, and the 3D printing technique can help to overcome these difficulties and not only serve as a microenvironment for cell infiltration but also provide localized gene release in a more sustainable way to induce effective cell differentiation. Herein, the cell transfection with plasmid DNA directly incorporated into sodium alginate prior to 3D printing was investigated both in vitro and in vivo. The 3D cryoprinting ensures pDNA structure integrity and safety. 3D printed gene-activated scaffolds (GAS) mediated HEK293 transfection in vitro and effective synthesis of model EGFP protein in vivo, thereby allowing the implementation of the developed GAS in future tissue engineering applications.
Keyphrases
- tissue engineering
- genome wide
- copy number
- gene therapy
- single cell
- genome wide identification
- cell therapy
- escherichia coli
- healthcare
- primary care
- stem cells
- dna methylation
- quality improvement
- carbon dioxide
- small molecule
- drug delivery
- amino acid
- cell free
- protein protein
- current status
- bone marrow
- atomic force microscopy
- wound healing