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PMID: 11849443 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Paradigm shift from classic anatomic theories to contemporary cell biological views of CAKUT.

Kidney international ·Vol. 61 ·No. 3 ·2002-03-00 ·Pages 889-98

Ichikawa I, Kuwayama F, Pope JC, Stephens FD, Miyazaki Y

Abstract

Ectopic budding of the ureter from the Wolffian duct is the first ontogenic misstep that leads to many-if not all-congenital anomalies of the kidney and urinary tract (CAKUT). The ectopia results in hypoplastic kidney, ectopia of ureterovesical orifice, urinary outflow obstruction and/or reflux. Studies in several mutant mouse models have verified that ectopic ureteric budding indeed precedes formation of CAKUT. Often, the genes involved in navigating ureteric budding to the correct site also regulate later ontogenic events of the kidney and urinary tract. The wide spectrum of CAKUT, for example, multicystic dysplastic kidney, megaureter and atretic ureter, portray the additional important functions of these same genes that are activated at multiple sites and stages during the normal morphogenesis of the kidney and urinary tract

MeSH Terms
Animals Cell Physiological Phenomena Congenital Abnormalities/genetics Embryonic and Fetal Development Genes, Regulator/physiology Humans Kidney/abnormalities Models, Anatomic Receptors, Angiotensin/genetics,physiology Ureter/embryology
Chemicals
Receptors, Angiotensin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ichikawa Iekuni
Department of Pediatrics, Vanderbilt University Medical Center, MCN C4204, 21st and Garland Avenue, Nashville, TN 37232-2584, USA. iekunii@aol.com
Kuwayama Fumiyo
Pope John C
Stephens F Douglas
Miyazaki Yoichi
Article Info
Journal
Kidney international
Abbr.
Kidney Int
ISSN
0085-2538
Published
2002-03-00
Pages
889-98
Language
English
Region
United States
NLM ID
0323470
Subset
IM
Grants
NIDDK NIH HHS · DK 37868 · United States
NIDDK NIH HHS · DK 44757 · United States
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