Fm. Lupinetti et al., PROCOLLAGEN PRODUCTION IN FRESH AND CRYOPRESERVED AORTIC-VALVE GRAFTS, Journal of thoracic and cardiovascular surgery, 113(1), 1997, pp. 102-107
Long-term durability of aortic valve allografts may be enhanced by cel
lular capacities for regeneration and repair. To evaluate aortic valve
graft production of an important structural protein, rat aortic roots
were implanted heterotopically into the abdominal aorta of recipient
rats, Grafts were either syngeneic or strongly allogeneic, were implan
ted either fresh or after cryopreservation, and were left in place 2 t
o 21 days after implantation, A total of 80 aortic valve grafts and th
e corresponding native aortic valves were examined, The grafts were re
trieved and immunocytochemically stained for the presence of procollag
en, a precursor to collagen, Regardless of histocompatibility or prese
rvation, grafts exhibited consistent procollagen presence that equaled
or exceeded that seen in the corresponding native valves, Positive pr
ocollagen staining was predominantly in the aortic wall, The most prom
inent staining was near the hinge point of the valve leaflets, with no
staining in the free portion of the leaflets, Staining with alpha-act
in demonstrated vascular smooth muscle in sites remote from the areas
positive for procollagen, which suggests that vascular smooth muscle w
as not responsible for the procollagen production, These findings indi
cate that cryopreservation is compatible with persistent fibroblast vi
ability and in vivo protein synthesis by both syngeneic and allogeneic
aortic valve grafts.