Control of mammalian kidney development by the Hedgehog signaling pathway

被引:34
作者
Cain, Jason E. [1 ,2 ]
Rosenblum, Norman D. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Hosp Sick Children, Div Nephrol, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Program Dev & Stem Cell Biol, Toronto, ON M5G 1L7, Canada
[3] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Pediat, Toronto, ON M5G 1X8, Canada
[5] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
关键词
Sonic hedgehog; Renal development; Hh signaling; GLI3; Patched; PALLISTER-HALL SYNDROME; CONGENITAL HYPOTHALAMIC HAMARTOBLASTOMA; GOLABI-BEHMEL-SYNDROME; BASAL-CELL CARCINOMA; SONIC HEDGEHOG; CUBITUS-INTERRUPTUS; TERMINAL DELETION; INDIAN HEDGEHOG; CHROMOSOME; 7Q; HUMAN HOMOLOG;
D O I
10.1007/s00467-010-1704-x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The kidney is the most common site of congenital malformations that result in impaired renal function. Yet, the molecular mechanisms that control renal malformations are poorly understood. The Hedgehog signaling pathway plays critical roles during mammalian organogenesis. Aberrant Hedgehog signaling results in severe congenital abnormalities, including renal malformations. Here, we review the current body of knowledge on Hedgehog signaling during renal morphogenesis and highlight the gaps in our understanding. Furthermore, we propose mechanisms by which Hedgehog signaling contributes to both normal and abnormal renal development.
引用
收藏
页码:1365 / 1371
页数:7
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