Format

Send to

Choose Destination
J Biomed Biotechnol. 2010;2010:696034. doi: 10.1155/2010/696034. Epub 2009 Dec 13.

Phenotypic transition of the collecting duct epithelium in congenital urinary tract obstruction.

Author information

1
Child and Family Research Institute, University of British Columbia, Vancouver, BC, Canada V5Z 4H4.

Abstract

Epithelial-mesenchymal transition (EMT) has emerged in recent years as an important process in the development of organ fibrosis in many human diseases. Our previous experience in a nonhuman primate model of obstructive nephropathy suggested that EMT of collecting duct epithelium contributes to the development of interstitial fibrosis. In this study we demonstrate for the first time in humans that obstructed fetal collecting duct epithelium undergoes transition to mesenchymal phenotype, characterized by decreased expression of epithelial markers, de novo expression of mesenchymal markers with subsequent loss of cell-cell interaction, disruption of the basement membrane, and increased deposition of extracellular matrix into the expanded interstitium of the obstructed kidney. The results of this study therefore support the previous findings from animal studies and suggest that EMT of the collecting duct epithelium might contribute to the development of interstitial fibrosis in human fetal obstructive nephropathy.

PMID:
20037736
PMCID:
PMC2796364
DOI:
10.1155/2010/696034
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Hindawi Limited Icon for PubMed Central
Loading ...
Support Center