Key result
FISH reveals donor cell persistence and host cell ingrowth in porcine aortic homografts at 4 months.
Why the study?
The pathogenesis of primary tissue degeneration limiting homograft life-span remains unknown, with prior histopathological studies lacking definitive insight into donor cell fate and host cell ingrowth.
Can fluorescence in situ hybridization (FISH) identify host and donor cells in porcine homograft heart valve explants?
Can fluorescence in situ hybridization (FISH) identify host and donor cells in porcine homograft heart valve explants?
FISH is a viable technique to distinguish host and donor cells in homograft heart valves, providing a tool to study tissue degeneration mechanisms.
Answers are grounded in this paper and cite their sources.
Should not yet change homograft valve practice; supports FISH as tool to study tissue degeneration mechanisms.
The pathogenesis of the primary tissue degeneration that limits the life-span of aortic and pulmonary homografts has still not been revealed. Histopathological studies on homograft explants have not given definitive insight into the eventual fate of donor cells, nor have they demonstrated the assumed importance of host cell ingrowth into the graft tissue. In this experimental study, fluorescence in situ hybridization (FISH) is introduced as a new approach to examine the distribution of host and donor cells in homograft explants. Aortic valve replacement was performed with a cryopreserved porcine aortic homograft in three pigs; donor and recipient were of opposite sex. After 4 months, the grafts were explanted and examined by FISH using a biotinylated porcine Y-chromosome-specific library probe. Following probe detection with FITC-conjugated avidin, a clear distinction could be made between cells of host and donor origin without distorting the histological integrity of the explants. There was ingrowth of donor cells into the graft aortic wall and into the valve leaflet, to some extent. In all explants, remaining donor cells were present, though decreased in number. The introduction of FISH in homograft heart valve research provides a powerful tool to study the fate of recipient and donor cellular elements in situ, and may therefore contribute to a better understanding of the histopathological processes that take place in transplanted homograft valves.
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Braun et al. (1997) studied this question. FISH enabled identification of both donor and host cells in porcine aortic homograft valves after 4 months, showing donor cell persistence and host cell ingrowth.
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