During bladder development, undifferentiated mesenchymal and epithelia
l cells undergo an orderly sequence of differentiation defined by the
expression of smooth-muscle (alpha-actin, myosin, vinculin, desmin, vi
mentin, and laminin) and epithelial (cytokeratins 5, 7, 8, 14, 18 and
19) protein markers. This process requires mesenchymal-epithelial inte
ractions with bladder epithelium (urothelium) necessary for the differ
entiation of bladder smooth muscle. Peptide growth factors such as ker
atinocyte growth factor (KGF) and transforming growth factors (TGF) al
pha and beta are likely candidates as mediators of these mesenchymal-e
pithelial interactions. Transcripts for KGF, TGF alpha, and TGF beta a
re regulated during bladder development and during smooth-muscle hyper
trophy secondary to bladder-outlet obstruction. Finally, two experimen
tal bladder models - (1) partial outlet obstruction and (2) regenerati
on of bladder smooth muscle into an acellular tissue matrix - are desc
ribed in the context of mesenchymal-epithelial interactions in the bla
dder.