Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/96101
Title: Engraftment Potential of Adipose Tissue-Derived Human Mesenchymal Stem Cells After Transplantation in the Fetal Rabbit
Author: Martínez-González, Itziar
Moreno, Rafael
Petriz, Jordi
Gratacós Solsona, Eduard
Aran, Josep M.
Keywords: Cèl·lules mare
Teixit adipós
Animals de laboratori
Stem cells
Adipose tissues
Laboratory animals
Issue Date: 31-Jul-2012
Publisher: Mary Ann Liebert, Inc.
Abstract: Due to their favorable intrinsic features, including engraftment, differentiation, and immunomodulatory potential, adult mesenchymal stem cells (MSCs) have been proposed for therapeutic in utero intervention. Further improvement of such attributes for particular diseases might merely be achieved by ex vivo MSC genetic engineering previous to transplantation. Here, we evaluated for the first time the feasibility, biodistribution, long-term engraftment, and transgenic enhanced green fluorescent protein (EGFP) expression of genetically engineered human adipose tissue-derived MSCs (EGFP+-ASCs) after intra-amniotic xenotransplantation at E17 of gestation into our validated pregnant rabbit model. Overall, the procedure was safe (86.4% survival rate; absence of anatomical defects). Stable, low-level engraftment of EGFP+-ASCs was confirmed by assessing the presence of the pWT-EGFP lentiviral provirus in the young transplanted rabbit tissues. Accordingly, similar frequencies of provirus-positive animals were found at both 8 weeks (60%) and 16 weeks (66.7%) after in utero intervention. The presence of EGFP+-ASCs was more frequent in respiratory epithelia (lung and trachea), according to the route of administration. However, we were unable to detect EGFP expression, neither by real-time polymerase chain reaction nor by immunohistochemistry, in the provirus-positive tissues, suggesting EGFP transgene silencing mediated by epigenetic events. Moreover, we noticed lack of both host cellular immune responses against xenogeneic ASCs and humoral immune responses against transgenic EGFP. Therefore, the fetal microchimerism achieved by the EGFP+-ASCs in the young rabbit hosts indicates induction of donor-specific tolerance after fetal rabbit xenotransplantation, which should boost postnatal transplantation for the early treatment/prevention of many devastating congenital disorders.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1089/scd.2012.0032
It is part of: Stem Cells and Development, 2012, vol. 21, num. 18, p. 3270-3277
Related resource: http://dx.doi.org/10.1089/scd.2012.0032
URI: http://hdl.handle.net/2445/96101
ISSN: 1547-3287
Appears in Collections:Articles publicats en revistes (Fonaments Clínics)

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