TY - JOUR
T1 - Molecular, cellular and developmental biology of urothelium as a basis of bladder regeneration
AU - Staack, Andrea
AU - Hayward, Simon W.
AU - Baskin, Laurence S.
AU - Cunha, Gerald R.
N1 - Funding Information:
Acknowledgments This study was supported by RO1 DK57246, R01 DK067049, CA84294, and CA89520. The authors thank Joel Brody for preparation of the figures.
PY - 2005/4
Y1 - 2005/4
N2 - Urinary bladder malfunction and disorders are caused by congenital diseases, trauma, inflammation, radiation, and nerve injuries. Loss of normal bladder function results in urinary tract infection, incontinence, renal failure, and end-stage renal dysfunction. In severe cases, bladder augmentation is required using segments of the gastrointestinal tract. However, use of gastrointestinal mucosa can result in complications such as electrolyte imbalance, stone formation, urinary tract infection, mucous production, and malignancy. Recent tissue engineering techniques use acellular grafts, cultured cells combined with biodegradable scaffolds, and cell sheets. These techniques are not all currently applicable for human bladder reconstruction. However, new avenues for bladder reconstruction maybe facilitated by a better understanding of urogenital development, the cellular and molecular biology of urothelium, and cell-cell interactions, which modulate tissue repair, homeostasis, and disease progression.
AB - Urinary bladder malfunction and disorders are caused by congenital diseases, trauma, inflammation, radiation, and nerve injuries. Loss of normal bladder function results in urinary tract infection, incontinence, renal failure, and end-stage renal dysfunction. In severe cases, bladder augmentation is required using segments of the gastrointestinal tract. However, use of gastrointestinal mucosa can result in complications such as electrolyte imbalance, stone formation, urinary tract infection, mucous production, and malignancy. Recent tissue engineering techniques use acellular grafts, cultured cells combined with biodegradable scaffolds, and cell sheets. These techniques are not all currently applicable for human bladder reconstruction. However, new avenues for bladder reconstruction maybe facilitated by a better understanding of urogenital development, the cellular and molecular biology of urothelium, and cell-cell interactions, which modulate tissue repair, homeostasis, and disease progression.
KW - Bladder reconstruction
KW - Embryology
KW - Tissue engineering
KW - Urothelium
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U2 - 10.1111/j.1432-0436.2005.00014.x
DO - 10.1111/j.1432-0436.2005.00014.x
M3 - Review article
C2 - 15901280
SN - 0301-4681
VL - 73
SP - 121
EP - 133
JO - Differentiation
JF - Differentiation
IS - 4
ER -