Background. Proximal pulmonary artery segment (PPAS) endothelial transfecti
on of lung grafts may be useful in ameliorating ischemia-reperfusion injury
and rejection and may provide beneficial downstream effects on the whole l
ung graft. Transfection immediately after lung transplantation may be effic
acious in ameliorating allograft dysfunction after transplantation.
Methods. In F344 rats, the PPAS was isolated and injected with 0.03 mt of G
L-67/DOPE-chloramphenicol acetyl transferase (CAT) plasmid DNA. The PPASs w
ere exposed for 60 minutes at several temperatures. The lung grafts were st
ored in saline solution (group 1, n = 24) or LPDG solution (group 2, n = 27
) for 12 or 24 hours at 4 degrees to 37 degrees C. In group 3 (n = 42), PPA
Ss were stored in endothelial cell culture medium and incubated at 10 degre
es or 37 degrees C in a carbon dioxide incubator for 3 to 72 hours. Group 4
(n = 18) served as transplanted controls; after 3 to 24 hours' preservatio
n at 4 degrees C in LPDG solution, lung grafts were transplanted. Transgene
expression of PPASs was assessed with two CAT activity assays, thin-layer
chromatography enzyme-linked immunosorbent assay and immediately after the
preservation period (groups 1 to 3) or 24 hours after transplantation (grou
p 4).
Results. In group 1, transgene expression did not appear. In groups 2 and 3
, transgene expression was apparent after any storage duration at 37 degree
s C. Transgene expression increased successively with longer storage period
s. In group 4, transgene expression was detected after any storage duration
. The enzyme-linked immunosorbent assay is able to quantify the expression
of CAT activity, but thin-layer chromatography is more sensitive.
Conclusions. Transgene expression did not occur during conventional cold st
orage. Transgene expression in rat PPASs during storage is possible with wa
rm storage (37 degrees C) and appropriate storage solution. (C) 1999 by The
Society of Thoracic Surgeons.