The pig represents the xenogeneic donor of choice for future organ transplantation in humans for anatomical and physiological reasons. However, to bypass several immunological barriers, strong and stable human genes expression must occur in the pig's organs. In this study we created transgenic pigs using in vitro transfection of cultured cells combined with somatic cell nuclear transfer (SCNT) to evaluate the ubiquitous transgene expression driven by pCAGGS vector in presence of different selectors. pCAGGS confirmed to be a very effective vector for ubiquitous transgene expression, irrespective of the selector that was used. Green fluorescent protein (GFP) expression observed in transfected fibroblasts was also maintained after nuclear transfer, through pre- and postimplantation development, at birth and during adulthood. Germ line transmission without silencing of the transgene was demonstrated. The ubiquitous expression of GFP was clearly confirmed in several tissues including endothelial cells, thus making it a suitable vector for the expression of multiple genes relevant to xenotransplantation where tissue specificity is not required. Finally cotransfection of green and red fluorescence protein transgenes was performed in fibroblasts and after nuclear transfer blastocysts expressing both fluorescent proteins were obtained.
|Titolo:||Transgene expression of green fluorescent protein and germ line transmission in cloned pigs derived from in vitro transfected adult fibroblasts|
|Parole Chiave:||Genetic Engineering ; Somatic Cell Nuclear Transfer ; Porcine ; Xenotransplantation ; matrix attachment regions ; mediated gene-transfer ; nuclear transfer ; plant-cells ; embryos ; tobacco ; cattle ; xenotransplantation ; efficiency ; selection|
|Data di pubblicazione:||dic-2008|
|Digital Object Identifier (DOI):||10.1089/clo.2008.0036|
|Appare nelle tipologie:||01 - Articolo su periodico|