Purpose: Recent advances in cell biology and tissue engineering have involv
ed various avascular or acellular scaffolds with or without seeded cells. T
hese techniques are frequently complicated by tissue necrosis, contracture
and resorption. We used a vascularized matrix prelaminated with autologous
cultured urothelial cells to reconstruct bladder wall defects.
Materials and Methods: A silicone block inserted into the right groin of 50
male Wistar rats directly superficial to the inferior epigastric vessels w
as used to induce capsule pouch formation. Urothelial cells harvested simul
taneously and cultured mere then suspended in fibrin glue and seeded into t
he newly formed capsule after removing the silicone block. After 1 week the
prelaminated nap was transposed into a surgically created bladder wall def
ect. Experimental groups included rats with a urothelial cell seeded capsul
e pouch sacrificed at 1 and 4 weeks, respectively, after bladder reconstruc
tion. In control rats scaffolds were treated only with fibrin glue or salin
e before transposition.
Results: Hematoxylin and eosin and immunohistochemical staining showed a co
ntinuous multilayered urothelial Lining along the transposed prelaminated c
apsule flap in the experimental groups with better survival compared to con
trols treated only with fibrin glue (80% mortality) or saline (100% mortali
ty). The surviving 3 control animals did not have a urothelial lining.
Conclusions: Vascularized prefabricated flaps lined with culture derived ur
othelial cells were successfully used for bladder reconstruction in a rat m
odel. The technique of prefabricating a vascularized scaffold lined with au
tologous urothelial cells may provide a method for future reconstruction of
the genitourinary systems.