Fibroblast growth factor-10 signals development of von Brunn's nests in the exstrophic bladder

Rocky Eastman, Elizabeth M. Leaf, Dianzhong Zhang, Lawrence D. True, Robert M. Sweet, Kristy Seidel, Joseph R. Siebert, Richard Grady, Michael E. Mitchell, James A. Bassuk

Research output: Contribution to journalArticlepeer-review

7 Scopus citations


Von Brunn's nests have long been recognized as precursors of benign lesions of the urinary bladder mucosa. We report here that von Brunn's nests are especially prevalent in the exstrophic bladder, a birth defect that predisposes the patient to formation of bladder cancer. Cells of von Brunn's nest were found to coalesce into a stratified, polarized epithelium which surrounds itself with a capsule-like structure rich in types I, III, and IV collagen. Histocytochemical analysis and keratin profiling demonstrated that nested cells exhibited a phenotype similar, but not identical, to that of urothelial cells of transitional epithelium. Immunostaining and in situ hybridization analysis of exstrophic tissue demonstrated that the FGF-10 receptor is synthesized and retained by cells of von Brunn's nest. In contrast, FGF-10 is synthesized and secreted by mesenchymal fibroblasts via a paracrine pathway that targets basal epithelial cells of von Brunn's nests. Small clusters of 10pRp cells, positive for both FGF-10 and its receptor, were observed both proximal to and inside blood vessels in the lamina propria. The collective evidence points to a mechanism where von Brunn's nests develop under the control of the FGF-10 signal transduction system and suggests that 10pRp cells may be the original source of nested cells.

Original languageEnglish (US)
Pages (from-to)F1094-F1110
JournalAmerican Journal of Physiology - Renal Physiology
Issue number5
StatePublished - Nov 2010


  • Bladder
  • Epithelium
  • Exstrophy
  • Growth factors
  • Lamina propria
  • Urothelium


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