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

被引:141
作者
Ichikawa, I
Kuwayama, F
Pope, JC
Stephens, FD
Miyazaki, Y
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Med Ctr, Dept Urol Surg, Nashville, TN 37232 USA
[4] Tokai Univ, Sch Med, Dept Pediat, Isehara, Kanagawa 25911, Japan
[5] Royal Childrens Hosp, Dept Surg, Melbourne, Vic, Australia
[6] Jikei Univ, Sch Med, Dept Med, Tokyo, Japan
关键词
congenital anomalies; urinary tract; kidney; ectopic budding; hypoplastic kidney; megaureter; atretic ureter; morphogenesis;
D O I
10.1046/j.1523-1755.2002.00188.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:889 / 898
页数:10
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