Crosstalk between VEGF-A/VEGFR2 and GDNF/RET signaling pathways.
Crosstalk between VEGF-A/VEGFR2 and GDNF/RET signaling pathways.
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DOI：
10.1016/j.bbrc.2007.04.146
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发表时间：
2007-06
影响因子：
3.1
通讯作者：
A. Tufro;Jason Teichman;N. Banu;Guillermo Villegas
中科院分区：
文献类型：
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作者：
A. Tufro;Jason Teichman;N. Banu;Guillermo Villegas
Vascular endothelial growth factor (VEGF-A) plays multiple roles in kidney development: stimulates cell proliferation, survival, tubulogenesis, and branching morphogenesis. However, the mechanism that mediates VEGF-A induced ureteric bud branching is unclear. Glial-derived neurotrophic factor (GDNF) signaling through tyrosine kinase c-RET is the major regulator of ureteric bud branching. Here we examined whether VEGF-A regulates RET signaling. We determined that ureteric bud-derived cells express the main VEGF-A signaling receptor, VEGFR2 and RET, by RT-PCR, immunoblotting, and immunocytochemistry. We show that the VEGF-A isoform VEGF165induces RET-tyr1062phosphorylation in addition to VEGFR2 autophosphorylation, that VEGF165and GDNF have additive effects on RET-tyr1062phosphorylation, and that VEGFR2 and RET co-immunoprecipitate. Functionally, VEGF165induces ureteric bud cell proliferation and branching morphogenesis. Similarly, in embryonic kidney explants VEGF165induces RET-tyr1062phosphorylation and upregulates GDNF. These findings provide evidence for a novel cooperative interaction between VEGFR2 and RET that mediates VEGF-A functions in ureteric bud cells.
