In Vitro Evaluation of Scaffolds for the Delivery of Mesenchymal Stem Cells to Wounds
Author
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Wahl, Elizabeth A.
Author
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Fierro, Fernando A.
Author
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Peavy, Thomas R.
Author
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Hopfner, Úrsula
Author
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Dye, Julian F.
Author
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Machens, Hans Günther
Author
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Egaña, José T.
Author
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Schenck, Thilo L.
Admission date
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2015-12-15T13:54:59Z
Available date
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2015-12-15T13:54:59Z
Publication date
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2015
Cita de ítem
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BioMed Research International
Volume 2015, Article ID 108571, 14 pages
en_US
Identifier
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DOI: 10.1155/2015/108571
Identifier
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https://repositorio.uchile.cl/handle/2250/135729
General note
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Artículo de publicación ISI
en_US
Abstract
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Mesenchymal stemcells (MSCs) have been shown to improve tissue regeneration in several preclinical and clinical trials. These cells have been used in combination with three-dimensional scaffolds as a promising approach in the field of regenerative medicine. We compare the behavior of human adipose-derived MSCs (AdMSCs) on four different biomaterials that are awaiting or have already received FDA approval to determine a suitable regenerative scaffold for delivering these cells to dermal wounds and increasing healing potential. AdMSCs were isolated, characterized, and seeded onto scaffolds based on chitosan, fibrin, bovine collagen, and decellularized porcine dermis. In vitro results demonstrated that the scaffolds strongly influence key parameters, such as seeding efficiency, cellular distribution, attachment, survival, metabolic activity, and paracrine release. Chick chorioallantoic membrane assays revealed that the scaffold composition similarly influences the angiogenic potential of AdMSCs in vivo. The wound healing potential of scaffolds increases by means of a synergistic relationship between AdMSCs and biomaterial resulting in the release of proangiogenic and cytokine factors, which is currently lacking when a scaffold alone is utilized. Furthermore, the methods used herein can be utilized to test other scaffold materials to increase their wound healing potential with AdMSCs.
en_US
Patrocinador
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CIRM-BMBF Early Translational II Award
FONDAP Center for Genome regulation
15090007