Surface modification of pig endothelial cells with a branched heparin conjugate improves their compatibility with human blood.

Bongoni, Anjan K; Salvaris, Evelyn; Nordling, Sofia; Klymiuk, Nikolai; Wolf, Eckhard; Ayares, David L; Rieben, Robert; Magnusson, Peetra U; Cowan, Peter J (2017). Surface modification of pig endothelial cells with a branched heparin conjugate improves their compatibility with human blood. Scientific Reports, 7(1), p. 4450. Nature Publishing Group 10.1038/s41598-017-04898-w

Preview

Text s41598-017-04898-w.pdf - Published Version Available under License Creative Commons: Attribution (CC-BY). Download (2MB) | Preview

Corline Heparin Conjugate (CHC), a compound of multiple unfractionated heparin chains, coats cells with a glycocalyx-like layer and may inhibit (xeno)transplant-associated activation of the plasma cascade systems. Here, we investigated the use of CHC to protect WT and genetically modified (GTKO.hCD46.hTBM) pig aortic endothelial cells (PAEC) in two pig-to-human in vitro xenotransplantation settings. Model 1: incubation of untreated or hTNFα-treated PAEC with 10% human plasma induced complement C3b/c and C5b-9 deposition, cellular activation and coagulation activation in WT and GTKO.hCD46.hTBM PAEC. Coating of untreated or hTNFα-treated PAEC with CHC (100 µg/ml) protected against human plasma-induced endothelial activation and damage. Model 2: PAEC were grown on microcarrier beads, coated with CHC, and incubated with non-anticoagulated whole human blood. Genetically modified PAEC significantly prolonged clotting time of human blood (115.0 ± 16.1 min, p < 0.001) compared to WT PAEC (34.0 ± 8.2 min). Surface CHC significantly improved the human blood compatibility of PAEC, as shown by increased clotting time (WT: 84.3 ± 11.3 min, p < 0.001; GTKO.hCD46.hTBM: 146.2 ± 20.4 min, p < 0.05) and reduced platelet adhesion, complement activation, coagulation activation and inhibition of fibrinolysis. The combination of CHC coating and genetic modification provided the greatest compatibility with human blood, suggesting that pre-transplant perfusion of genetically modified porcine organs with CHC may benefit post-transplant xenograft function.

Interest & Impact

Downloads

140 since deposited on 02 Feb 2018
16 in the past 12 months

Citations

5 Citations in Web of Science ®
6 Citations in Scopus

Search

in Google Scholar™

Services

Actions (login required)

Edit item

Actions (login required)

Edit item