Objective: Dilatation and valve regurgitation are disturbing sequelae of th
e pulmonary root functioning at systemic pressures. We tried to characteriz
e the histologic mode of adaptation of the neoaortic wall.
Methods: We compared routine histologic studies, immunohistochemical staini
ng, and computer-assisted morphometric analysis of aortic, pulmonary autogr
aft, and native pulmonary wall specimens from pigs in which, as a newborn,
a valveless pulmonary autograft had been implanted in the aorta.
Results: Histologic examination of the pulmonary autograft revealed a viabl
e, normally revascularized wall without degenerative phenomena. Smooth musc
le cells were enlarged and rearranged. The characteristic "pulmonary" media
l elastin lamellar structure was retained, which was confirmed by morphomet
ry. Immunohistochemistry of the autograft revealed relatively strong staini
ng of type III collagen and alpha smooth muscle actin, exclusive staining o
f basic fibroblast growth factor, and no staining of proliferation markers
proliferating cell nuclear antigen and Ki67.
Conclusion: The developing pulmonary autograft in the aortic position becom
es normally revascularized, lacks major degenerative phenomena, and retains
its own typical pulmonary morphologic features. Remodeling is accomplished
by increased extracellular matrix deposition with collagen as an important
constituent. The marked expression of growth factors in the autograft sugg
ests the persistence of increased metabolic activity.