Title:
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Over-Expression of Ecto-5'-Nucleotidase in Pig Endothelial Cells
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Ecto-5'-nucleotidase (E5'N) is an endothelial surface enzyme that controls conversion of
extracellular nucleotides into immunosuppressive adenosine. Species differences and
especially lO-fold higher activity of E5'N in human endothelial cells (EC) than in pig EC
could be important barrier for xenotransplantation.The major aim ofmy thesis is evaluation
whether expression of human E5'N on pig EC is able to attenuate cell death mediated by
components ofhuman blood responsible for delayed xenograft rejection (DXR).
A pig cell line was transfected with human E5'N and efficiency assessed with flow cytometry
and nucleotide breakdown assays using cell monolayers and lysates. Transfected cells were
>95% positive for human E5'N/There was a massive increase in E5'N activity in transfected
pig EC lysates and intact cells using extracellu~ar AMP as the substrate. Adenosine
production from the breakdown of ATP was also significantly higher in transfected cells,
proving E5'N to be the rate-limiting enzyme in adenosine production by pig EC.
Incubation of transfected cells with AMP showed a time-dependent induction of the antiapoptotic
protein Bcl-2 mediated via AI receptors, and subsequent protection of these cells
from hydrogen peroxide-mediated apoptosis through AI receptors. Human natural killer (NK)
cells were significantly less cytotoxic towards transfected than non-transfected pig EC. This
effect was abrogated by an inhibitor of E5'N and mimicked by prior incubation of NK cells
with adenosine. Supernatants from transfected cells also significantly inhibited platelet
aggregation and expression of E5'N attenuated platelet adhesion to EC compared to nontransfected
cells. However, transfection with E5'N did not protect cells from antibody and
complement-mediated cytotoxicity.
Functional expression of human E5'N in pig EC provided significant protection from
apoptosis, NK cell-mediated lysis and platelet adhesion and aggregation, the main
mechanisms of xenograft r~jection once hyperacute rejection has been overcome. E5'N is
thus a potential candidate for. engineering of transgenic animals for xenotransplantation.
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