In vivo replacement of damaged bladder urothelium by Wolffian duct epithelial cells. Joseph, D., Chandrashekar, A., Abler, L., Chu, L., Thomson, J., Mendelsohn, C, & Vezina, C. Proceedings of the National Academy of Sciences of the United States of America, 115(33):8394–8399, August, 2018.
doi  abstract   bibtex   
The bladder's remarkable regenerative capacity had been thought to derive exclusively from its own progenitors. While examining consequences of DNA methyltransferase 1 (Dnmt1) inactivation in mouse embryonic bladder epithelium, we made the surprising discovery that Wolffian duct epithelial cells can support bladder regeneration. Conditional Dnmt1 inactivation in mouse urethral and bladder epithelium triggers widespread apoptosis, depletes basal and intermediate bladder cells, and disrupts uroplakin protein expression. These events coincide with Wolffian duct epithelial cell recruitment into Dnmt1 mutant urethra and bladder where they are reprogrammed to express bladder markers, including FOXA1, keratin 5, P63, and uroplakin. This is evidence that Wolffian duct epithelial cells are summoned in vivo to replace damaged bladder epithelium and function as a reservoir of cells for bladder regeneration.
@article{joseph_vivo_2018,
	title = {In vivo replacement of damaged bladder urothelium by {Wolffian} duct epithelial cells.},
	volume = {115},
	doi = {https://doi.org/10.1073/pnas.1802966115},
	abstract = {The bladder's remarkable regenerative capacity had been thought to derive exclusively from its own progenitors. While examining consequences of DNA methyltransferase 1 (Dnmt1) inactivation in mouse embryonic bladder epithelium, we made the surprising discovery that Wolffian duct epithelial cells can support bladder regeneration. Conditional Dnmt1 inactivation in mouse urethral and bladder epithelium triggers widespread apoptosis, depletes basal and intermediate bladder cells, and disrupts uroplakin protein expression. These events coincide with Wolffian duct epithelial cell recruitment into Dnmt1 mutant urethra and bladder where they are reprogrammed to express bladder markers, including FOXA1, keratin 5, P63, and uroplakin. This is evidence that Wolffian duct epithelial cells are summoned in vivo to replace damaged bladder epithelium and function as a reservoir of cells for bladder regeneration.},
	number = {33},
	journal = {Proceedings of the National Academy of Sciences of the United States of America},
	author = {Joseph, DB and Chandrashekar, AS and Abler, LL and Chu, LF and Thomson, JA and Mendelsohn, C and Vezina, CM},
	month = aug,
	year = {2018},
	pages = {8394--8399},
}

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