Long-term survival of small bowel transplants is hampered by chronic reject
ion. Epidermal growth factor (EGF) and transforming growth factor beta (TGF
-beta P) have opposing, regulatory roles in normal intestinal physiology an
d may be involved in the pathogenesis of chronic intestinal rejection. Our
aim was to investigate the expression of EGF and TGF-beta(1) in chronically
rejecting small bowel transplants. Orthotopic small bowel transplantation
was performed in the allogeneic DA-to-AS rat combination; Cyclosporin was a
dministered temporarily to prevent acute rejection. Controls were DA isogra
fts and normal DA rats. PreproECF and TGF-beta(1) gene expression was evalu
ated by northern blot analysis of the ileum RNA and standardized against gl
yceraldehyde-3-phosphate-dehydrogenase expression. Allografts demonstrated
functional impairment and histological features of chronic rejection, where
as isografts appeared normal. Allografts demonstrated a significant reducti
on of EGF mRNA when compared to DA isografts. No significant changes were d
etected in TGF-beta(1) expression in either allogeneic or syngeneic grafts.
In conclusion, this study demonstrates reduced preproEGF and preserved TGF
-beta(1) gene expression in chronically rejecting small bowel transplants.