INEB
INEB
TitleNon-viral gene delivery to mesenchymal stem cells: Methods, strategies and application in bone tissue engineering and regeneration
Publication TypeJournal Article
2011
AuthorsSantos, JL, Pandita, D, Rodrigues, J, Pêgo, AP, Granja, PL, Tomás, H
JournalCurrent Gene TherapyCurr. Gene Ther.
Volume11
Issue1
Pagination46 - 57
Date Published2011///
15665232 (ISSN)
Animals, article, artificial chromosome, Bone and Bones, Bone Regeneration, bone tissue, Bone tissue engineering, cell based gene therapy, dendrimer, ex vivo gene transfer, Gene delivery, gene targeting, Gene therapy, Gene Transfer Techniques, gene vector, genetic transfection, human, Humans, in vivo gene transfer, liposome, Mesenchymal stem cell, Mesenchymal Stem Cells, nanomedicine, nanoparticle, Non-viral vectors, nonhuman, nonviral gene delivery system, polymer, protein expression, Regeneration, Regenerative Medicine, Tissue engineering, Tissue regeneration
Mesenchymal stem cells (MSCs) can be isolated from several tissues in the body, have the ability to selfrenewal, show immune suppressive properties and are multipotent, being able to generate various cell types. At present, due to their intrinsic characteristics, MSCs are considered very promising in the area of tissue engineering and regenerative medicine. In this context, genetic modification can be a powerful tool to control the behavior and fate of these cells and be used in the design of new cellular therapies. Viral systems are very effective in the introduction of exogenous genes inside MSCs. However, the risks associated with their use are leading to an increasing search for non-viral approaches to attain the same purpose, even if MSCs have been shown to be more difficult to transfect in this way. In the past few years, progress was made in the development of chemical and physical methods for non-viral gene delivery. Herein, an overview of the application of those methods specifically to MSCs is given and their use in tissue engineering and regenerative medicine therapeutic strategies highlighted using the example of bone tissue. Key issues and future directions in non-viral gene delivery to MSCs are also critically addressed. © 2011 Bentham Science Publishers Ltd.
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