首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >JIP3 Mediates TrkB Axonal Anterograde Transport and Enhances BDNF Signaling by Directly Bridging TrkB with Kinesin-1.
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JIP3 Mediates TrkB Axonal Anterograde Transport and Enhances BDNF Signaling by Directly Bridging TrkB with Kinesin-1.

机译:JIP3通过直接将TrkB与Kinesin-1桥接来介导T​​rkB轴突顺行转运并增强BDNF信号传导。

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摘要

Brain-derived neurotrophic factor (BDNF), secreted from target tissues, binds and activates TrkB receptors, located on axonal terminals of the innervating neurons, and thereby initiates retrograde signaling. Long-range anterograde transport of TrkB in axons and dendrites requires kinesin-mediated transport. However, it remains unknown whether anterograde TrkB transport mechanisms are the same in axons versus in dendrites. Here, we show that c-Jun NH(2)-terminal kinase-interacting protein 3 (JIP3) binds directly to TrkB, via a minimal 12 aa domain in the TrkB juxtamembrane region, and links TrkB to kinesin-1. The JIP3/TrkB interaction selectively drives TrkB anterograde transport in axons but not in dendrites of rat hippocampal neurons. Moreover, we find that TrkB axonal transport mediated by JIP3 could regulate BDNF-induced Erk activation and axonal filopodia formation. Our findings demonstrate a role for JIP3-mediated TrkB anterograde axonal transport in recruiting more TrkB into distal axons and facilitating BDNF-induced retrograde signaling and synapse modulation, which provides a novel mechanism of how the TrkB anterograde transport can be coupled to BDNF signaling in distal axons.
机译:从目标组织分泌的脑源性神经营养因子(BDNF)结合并激活位于神经支配神经元轴突末端的TrkB受体,从而启动逆行信号传导。 TrkB在轴突和树突中的远距离顺行运输需要驱动蛋白介导的运输。但是,尚不清楚顺行的TrkB转运机制在轴突与树突中是否相同。在这里,我们显示c-Jun NH(2)-末端激酶相互作用蛋白3(JIP3)通过TrkB近膜区域中的最小12aa结构域直接结合到TrkB,并将TrkB链接到kinesin-1。 JIP3 / TrkB相互作用选择性驱动大鼠海马神经元树突中的TrkB顺行转运,而不是在大鼠海马神经元的树突中。此外,我们发现JIP3介导的TrkB轴突运输可以调节BDNF诱导的Erk激活和轴突丝状伪足的形成。我们的研究结果表明,JIP3介导的TrkB顺行轴突运输在向远端轴突募集更多TrkB并促进BDNF诱导的逆行信号和突触调节中发挥了作用,这为TrkB顺行运输如何与远端BDNF信号传导耦合提供了新机制。轴突。

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