The apical surface of mammalian bladder urothelium is almost completely covered by urothelial plaques consisting of 2D crystals of 16-nm uroplakin particles. We have shown that these urothelial plaques are composed of four major uroplakins (UPIa, Ib, II and IIIa), and have studied the structure, function and disease implications of these major urothelial differentiation products. During the previous grant period, we made several key advances, including the generation of uroplakin knockout mice demonstrating that uroplakins contribute to the urothelial permeability barrier function, the development of a technique to biotinylate the apical surface of mouse bladder urothelium, and the discovery of several novel urothelial organelles that we believe play central roles in uroplakin trafficking and urothelial membrane expansion and repair. These findings allow us to test three important hypotheses.
In Aim One, we will test the hypotheses that uroplakin endocytosis occurs via a novel, clathrin- and caveolin-independent process, and that uroplakin exocytosis plays a role in urothelial membrane expansion and repair.
In Aim Two, we will test the hypothesis that uroplakins can function, in addition to contributing to the permeability barrier function, in enhancing the urothelial surface's ability to withstand excessive stretch thus preventing it from rupturing during bladder distention.
In Aim Three, we will test the hypothesis that a novel urothelial organelle may play a key role in membrane expansion as well as repair. Our proposed studies wall utilize our uroplakin knockout mouse models, an in vivo tagging technique, and adenovirus to modulate, in vivo, key molecules in uroplakin trafficking. Our studies challenge some of the existing paradigms regarding urothelial membrane trafficking, address uroplakin functions in membrane stabilization, and elucidate the functional roles of novel urothelial organelles in membrane expansion and repair. Our results will enhance our understanding on how bladder urothelium functions under normal and over-stretched conditions, and have implications for important bladder conditions such as urinary tract obstruction and bacterial infection.

Public Health Relevance

Bladder epithelium forms a barrier between the urine and the blood, adjusts its surface area when the bladder is expanded, repairs itself when damaged, and provides the first line of defense against bacterial infection. Our proposed studies will improve our understnding on these important urothelial functions, and will have impact on bladder diseases including urinary tract infection, overactive bladder and urinary outlet obstruction.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK052206-13
Application #
8566106
Study Section
Special Emphasis Panel (ZDK1-GRB-S (M2))
Project Start
1999-03-01
Project End
2015-06-30
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
13
Fiscal Year
2012
Total Cost
$446,355
Indirect Cost
$169,319
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
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