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Dissertation/Thesis Abstract

Exocyst Dysfunction Leads to Defects in Urothelial Differention in a Novel Mouse Model of Congenital Ureter Obstructions
by Lee, Amanda, Ph.D., University of Hawai'i at Manoa, 2017, 107; 10656602
Abstract (Summary)

The exocyst is an eight protein trafficking complex responsible for polarized exocytosis of a certain subset of vesicles to the plasma membrane. The exocyst is present in a large variety of cell types and is involved in many different cellular processes. The protein, Sec10, has been reported to be a central component of the exocyst, and loss of this protein leads to inactivation of the entire complex. Here we show that the exocyst complex is essential for primary cilia formation, epithelial homeostasis, and cell survival in a cell culture model. We also report generation of a conditional knockout mouse for Sec10, which is the first conditional allele for any exocyst gene. Inactivation of Sec10 in ureteric bud derived cells results in severe bilateral hydronephrosis and complete anuria in newborns, with death occurring 6-14 hours after birth. Sec10 conditional knockout mice develop ureteropelvic junction obstructions between E17.5 and E18.5 due to failure of urothelial progenitor cells to differentiate into superficial cells, which are responsible for producing uroplakin plaques on the luminal surface. These Sec10 knockout urothelial cells undergo cell death by E17.5 and the urothelial barrier becomes leaky to luminal fluid. Also at E17.5, we measured increased expression of TGFβ1 and genes associated with myofibroblast activation, with evidence of stromal remodeling. Our findings support the model that a defective urothelial barrier allows urine to induce a fibrotic wound healing mechanism, which may contribute to human prenatal UPJ obstructions.

Indexing (document details)
Advisor: Fogelgren, Ben
Commitee: Berry, Marla, Lozanoff, Scott, Matsui, Takashi, Nerurkar, Pratibha
School: University of Hawai'i at Manoa
Department: Cell and Molecular Biology
School Location: United States -- Hawaii
Source: DAI-B 79/01(E), Dissertation Abstracts International
Subjects: Molecular biology, Cellular biology, Developmental biology
Keywords: Congenital obstructive nephropathy, Exocysts, Kidney development, Mouse model, Primary cilia, Ureter development
Publication Number: 10656602
ISBN: 978-0-355-26484-5
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