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ShcD interacts with TrkB via its PTB and SH2 domains and regulates BDNF-induced MAPK activation

机译:SHCD通过其PTB和SH2结构域与TRKB进行交互,并调节BDNF诱导的MAPK激活

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Neurotrophins regulate many aspects of neuronal function through activation of the high affinity Trk receptors. Shc family proteins are implicated in the coupling of RTK to the Ras/mitogen-activated protein kinase signaling cascade. Here we report that the fourth Shc family member, ShcD, associates with TrkB receptor and regulates BDNF-induced MAPK activation. Yeast two-hybrid assay and Co-IP experiments demonstrate ShcD interacts with TrkB in a kinase-activity-dependent manner. Confocal analysis shows ShcD cololizes well with TrkB in transfected 293T cells. Subsequent mapping experiments and mutational analysis indicate that both PTB and SH2 domains are capable of binding to TrkB and PTB domain binds to TrkB NPQY motif. Furthermore, ShcD is involved in BDNF-induced MAPK activation. In summary, we demonstrate that ShcD is a substrate of TrkB and mediates TrkB downstream signaling pathway.
机译:神经营养素通过激活高亲和力Trk受体来调节神经元功能的许多方面。 SHC系列蛋白质涉及RTK与RAS / mit-活化的蛋白激酶信号传导级联的偶联。在这里,我们报告说,第四世纪家庭成员,SHCD,与TRKB受体相关联,并调节BDNF诱导的MAPK激活。酵母双杂化测定和共同IP实验证明了SHCD以激酶活性依赖性方式与TRKB相互作用。共焦分析显示转染293T细胞中的TRKB细胞间良好。随后的映射实验和突变分析表明PTB和SH2结构域能够与TRKB和PTB结构域结合到TRKB NPQY基序。此外,SHCD参与了BDNF诱导的MAPK激活。总之,我们证明SHCD是TRKB的基材,并介导TRKB下游信号通路。

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