首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Identification of a Key Motif That Determines the Differential Surface Levels of RET and TrkB Tyrosine Kinase Receptors and Controls Depolarization Enhanced RET Surface Insertion
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Identification of a Key Motif That Determines the Differential Surface Levels of RET and TrkB Tyrosine Kinase Receptors and Controls Depolarization Enhanced RET Surface Insertion

机译:确定一个关键主题的决定该主题确定RET和TrkB酪氨酸激酶受体的差异表面水平并控制去极化增强的RET表面插入

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摘要

The RET tyrosine kinase receptor plays an important role in the development and maintenance of the nervous system. Although the ligand-induced RET signaling pathway has been well described, little is known about the regulation of RET surface expression, which is integral to the cell ability to control the response to ligand stimuli. We found that in dorsal root ganglion (DRG) neurons, which co-express RET and TrkB, the receptor surface levels of RET are significantly higher than that of TrkB. Using a sequence substitution strategy, we identified a key motif (Box1), which is necessary and sufficient for the differential RET and TrkB surface levels. Furthermore, pharmacological and mutagenesis assays revealed that protein kinase C (PKC) and high K+ depolarization increase RET surface levels through phosphorylation of the Thr675 residue in the Box1 motif. Finally, we found that the phosphorylation status of the Thr675 residue influences RET mediated response to GDNF stimulation. In all, these findings provide a novel mechanism for the modulation of RET surface expression.
机译:RET酪氨酸激酶受体在神经系统的发育和维持中起重要作用。尽管已经很好地描述了配体诱导的RET信号通路,但对RET表面表达的调节知之甚少,而RET表面表达是细胞控制对配体刺激的反应能力不可或缺的部分。我们发现在共表达RET和TrkB的背根神经节(DRG)神经元中,RET的受体表面水平显着高于TrkB。使用序列替换策略,我们确定了关键基序(Box1),这对于差异RET和TrkB表面水平是必要的和充分的。此外,药理和诱变分析表明,蛋白激酶C(PKC)和高K + 去极化通过Box1基序中的Thr 675 残基的磷酸化增加RET表面水平。最后,我们发现Thr 675 残基的磷酸化状态影响RET介导的GDNF刺激反应。总之,这些发现为调节RET表面表达提供了一种新颖的机制。

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