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1.
J Control Release ; 239: 137-48, 2016 10 10.
Article in English | MEDLINE | ID: mdl-27586186

ABSTRACT

Transcript therapies using chemically modified messenger RNAs (cmRNAs) are emerging as safe and promising alternatives for gene and recombinant protein therapies. However, their applications have been limited due to transient translation and relatively low stability of cmRNAs compared to DNA. Here we show that vacuum-dried cmRNA-loaded collagen sponges, termed transcript activated matrices (TAMs), can serve as depots for sustained delivery of cmRNA. TAMs provide steady state protein production for up to six days, and substantial residual expression until 11days post transfection. Another advantage of this technology was nearly 100% transfection efficiency as well as low toxicity in vitro. TAMs were stable for at least 6months at room temperature. Human BMP-2-encoding TAMs induced osteogenic differentiation of MC3T3-E1 cells in vitro and bone regeneration in a non-critical rat femoral bone defect model in vivo. In summary, TAMs are a promising tool for bone regeneration and potentially also for other applications in regenerative medicine and tissue engineering.


Subject(s)
Bone Regeneration/genetics , Collagen/administration & dosage , Gene Transfer Techniques , Genetic Therapy/methods , RNA, Messenger/administration & dosage , RNA, Messenger/genetics , A549 Cells , Animals , Bone Regeneration/drug effects , Cell Survival/drug effects , Cell Survival/physiology , Cells, Cultured , Collagen/chemistry , Collagen/metabolism , Delayed-Action Preparations/administration & dosage , Delayed-Action Preparations/chemistry , Delayed-Action Preparations/metabolism , Femur/diagnostic imaging , Femur/drug effects , Femur/metabolism , Hep G2 Cells , Humans , Male , Mice , NIH 3T3 Cells , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley
2.
Biomaterials ; 87: 131-146, 2016 May.
Article in English | MEDLINE | ID: mdl-26923361

ABSTRACT

Limitations associated to the use of growth factors represent a major hurdle to musculoskeletal regeneration. On the one hand, they are needed to induce neo-tissue formation for the substitution of a necrotic or missing tissue. On the other hand, these factors are used in supraphysiological concentrations, are short lived and expensive and result in many side effects. Here we develop a gene transfer strategy based on the use of chemically modified mRNA (cmRNA) coding for human bone morphogenetic protein 2 (hBMP-2) that is non-immunogenic and highly stable when compared to unmodified mRNA. Transfected stem cells secrete hBMP-2, show elevated alkaline phosphatase levels and upregulated expression of RunX2, ALP, Osterix, Osteocalcin, Osteopontin and Collagen Type I genes. Mineralization was induced as seen by positive Alizarin red staining. hBMP-2 cmRNA transfected human fat tissue also yielded an osteogenic response in vitro as indicated by expression of hBMP-2, RunX2, ALP and Collagen Type I. Delivering hBMP-2 cmRNA to a femur defect in a rat model results in new bone tissue formation as early as 2 weeks after application of very low doses. Overall, our studies demonstrate the feasibility and therapeutic potential of a new cmRNA-based gene therapy strategy that is safe and efficient. When applied clinically, this approach could overcome BMP-2 growth factor associated limitations in bone regeneration.


Subject(s)
Bone Morphogenetic Protein 2/genetics , Bone Regeneration , Femur/injuries , Osteogenesis , RNA, Messenger/therapeutic use , Stem Cells/cytology , Transfection , Animals , Bone Morphogenetic Protein 2/metabolism , Cells, Cultured , Femur/metabolism , Femur/pathology , Femur/physiology , Genetic Therapy/methods , Humans , Male , RNA, Messenger/chemistry , RNA, Messenger/genetics , Rats , Rats, Sprague-Dawley , Stem Cells/metabolism
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