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The overall goal of this project is to understand the mechanisms that control the growth, morphogenesis and differentiation of the ureteric bud during kidney development. While it is established that GDNF, signaling through the receptor tyrosine kinase Ret and the co-receptor GFRalpha1, plays an essential role in this process, the downstream mechanisms remain largely obscure. We hypothesize that GDNF regulates the expression of a set of target genes, which in turn mediate the different functions of the developing ureteric bud, including growth, branching morphogenesis, differentiation into specific collecting duct cell types, and production of factors that induce the mesenchymal stem cells to undergo nephrogenesis. In Aim 1 we propose to identify the target genes whose expression in the ureteric bud is induced or repressed by GDNF. Our preliminary data indicate that the screen will be highly effective and will allow us to identify a variety of genes with important and unforeseen roles in kidney development. In Aim 2 we propose to conduct several modified screens to investigate the mechanisms by which GDNF regulates the expression of its target genes, via different isoforms of the Ret receptor and different intracellular signaling pathways. In Aim 3 we propose a series of functional studies in mouse models to investigate the roles of several novel GDNF target genes in renal development. The initial target genes to be examined will include a chemokine receptor that may play a role in the regulation ofureteric bud branching, a secreted cytokine that may be involved in the induction of nephrogenesis, and a transcription factor that could mediate regulation of secondary target genes. The proposed methods include loss-of-function studies using knockout and other mutant mice, gain-of-function studies using transgenic mice, as well as in vitro organ culture experiments. In addition to being a fascinating problem in developmental biology, the control of ureteric bud morphogenesis has important clinical implications, as renal agenesis, ureteral defects and renal hypodysplasia are common birth defects that can of Len be attributed to defects in the development of the ureteric bud.
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Genetic analysis of Pea3 transcription factors and kidney development
Branching Morphogenesis of Urinary Epithelia: from Genes to Cellular Behaviors
Branching Morphogenesis of Urinary Epithelia: from Genes to Cellular Behaviors
Branching Morphogenesis of Urinary Epithelia: from Genes to Cellular Behaviors
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海外基金
分化肌细胞脱细胞ECM-cells sheet 3D 支架构建及其促进容积性肌组织缺损再 生修复应用及机制研究
CAFs-TAMs-tumor cells调控在HRHPV感染致癌中的作用机制研究及AI可追溯预测模型建立
  • 批准号:
    82072862
  • 项目类别:
    面上项目
  • 资助金额:
    56.0万元
  • 批准年份:
    2020
  • 负责人:
    徐云升
  • 依托单位:
S100A8/A9--Myeloid cells特异性可溶性表氧化物水解酶(sEH)基因敲除改善胰岛素抵抗的新靶点
  • 批准号:
    82070825
  • 项目类别:
    面上项目
  • 资助金额:
    53.0万元
  • 批准年份:
    2020
  • 负责人:
    徐西振
  • 依托单位:
Leader cells通过CCL5调控糖酵解及基质硬度促进结直肠癌集体侵袭的 作用机制
  • 批准号:
    81903002
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.5万元
  • 批准年份:
    2019
  • 负责人:
    王斐斐
  • 依托单位: