Semaphorin3a inhibits ureteric bud branching morphogenesis

被引:40
作者
Tufro, Alda [1 ]
Teichman, Jason
Woda, Craig
Villegas, Guillermo
机构
[1] Albert Einstein Coll Med, Dept Pediat, Bronx, NY 10461 USA
关键词
Sema3a; metanephric development; branching morphogenesis; plexins; GDNF/RET;
D O I
10.1016/j.mod.2007.12.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Class 3 semaphorins are guidance proteins involved in axon pathfinding, vascular patterning and lung branching morphogenesis in the developing mouse embryo. Semaphorin3a (Sema3a) is expressed in renal epithelia throughout kidney development, including podocytes and ureteric bud cells. However, the role of Sema3a in ureteric bud branching is unknown. Here we demonstrate that Sema3a plays a role in patterning the ureteric bud tree in both metanephric organ cultures and Sema3a mutant mice. In vitro ureteric bud injection with Sema3a antisense morpholino resulted in increased branching, whereas recombinant SEMA3A inhibited ureteric bud branching and decreased the number of developing glomeruli. Additional studies revealed that SEMA3A effects on ureteric bud branching involve downregulation of glial cell-line derived neurotrophic factor (GDNF) signaling, competition with vascular endothelial growth factor A (VEGF-A) and decreased activity of Akt survival pathways. Deletion of Sema3a in mice is associated with increased ureteric bud branching, confirming its inhibitory role in vivo. Collectively, these data suggest that Sema3a is an endogenous antagonist of ureteric bud branching and hence, plays a role in patterning the renal collecting system as a negative regulator. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:558 / 568
页数:11
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