Characterization of Three Generations of Transgenic Pigs Expressing the HLA-E Gene

Author:

Hryhorowicz Magdalena1,Zeyland Joanna1,Nowak-Terpiłowska Agnieszka1,Jura Jacek2,Juzwa Wojciech3,Słomski Ryszard14,Bocianowski Jan5,Smorąg Zdzisław2,Woźniak Anna6,Lipiński Daniel1

Affiliation:

1. Department of Biochemistry and Biotechnology , Poznan University of Life Sciences , Dojazd 11, 60-632 Poznań , Poland

2. Department of Animal Reproduction, National Research Institute of Animal Production , 32-083 Balice n. Kraków , Poland

3. Department of Biotechnology and Food Microbiology , Poznan University of Life Sciences , Wojska Polskiego 48, 60-627 Poznań , Poland

4. Institute of Human Genetics, Polish Academy of Sciences , Strzeszyńska 32, 60-101 Poznań , Poland

5. Department of Mathematical and Statistical Methods , Poznan University of Life Sciences , Wojska Polskiego 28, 60-637 Poznań , Poland

6. The NanoBioMedical Centre , Adam Mickiewicz University , Umultowska 85, 61-614 Poznań , Poland

Abstract

Abstract The use of pigs as a source of organs and tissues for xenotransplantation can overcome the growing shortage of human donors. Human NK cells play an important role in the cell-mediated rejection of pig-to-human xenografts. In this paper we report the generation and extensive characterization of three generations of transgenic pigs with HLA-E gene encoding the antigen which can inhibit the human NK cell-mediated response. The gene construct pHLAE-GFPBsd containing the human gene encoding the human leukocyte antigen under the promoter of the EF-1α elongation factor ensuring systemic expression was introduced by microinjection into a pronucleus of the fertilized porcine oocyte. PCR analysis revealed and FISH analysis confirmed that the pHLAE-GFPBsd gene construct was present in the genome of the founder female pig. As a result of inter-breeding, an additional 7 transgenic animals were obtained (one individual from F1 generation and six individuals from F2 generation). The transgene expression was shown by RT-PCR and flow cytometry. Real Time PCR analysis estimated the approximate number of transgene copies at 16–34. Karyotype analysis did not show any changes in the structure or the number of chromosomes. The expression level of the transgene was stable in the next generation of genetically modified pigs. An NK cell-mediated cytotoxicity assay showed the increased viability of the transgenic cells in comparison with the wild-type, which confirmed the protective influence of HLA-E expression.

Publisher

Walter de Gruyter GmbH

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