Department of Neurobiology, Shandong Provincial Key Laboratory of Mental Disorders, School of Medicine, Shandong University, Jinan, Shandong 250012, People's Republic of China.
J Neurosci. 2011 Jul 20;31(29):10602-14. doi: 10.1523/JNEUROSCI.0436-11.2011.
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.
脑源性神经营养因子(BDNF)由靶组织分泌,与位于支配神经元轴突末梢的 TrkB 受体结合并使其激活,从而启动逆行信号转导。TrkB 在轴突和树突中的长程顺行转运需要靠驱动蛋白介导的运输。然而,目前尚不清楚 TrkB 的顺行转运机制在轴突和树突中是否相同。本研究表明,c-Jun NH2-末端激酶相互作用蛋白 3(JIP3)通过 TrkB 跨膜区的一个最小的 12 个氨基酸结构域直接与 TrkB 结合,并将 TrkB 与驱动蛋白-1 连接。JIP3/TrkB 相互作用选择性地驱动 TrkB 在大鼠海马神经元的轴突中而不是树突中向前转运。此外,我们发现 JIP3 介导的 TrkB 顺行轴突转运可以调节 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 顺行轴突转运在将更多的 TrkB 募集到远端轴突中发挥作用,并促进 BDNF 诱导的逆行信号转导和突触调节,为 TrkB 顺行转运如何与远端轴突中的 BDNF 信号转导偶联提供了一种新的机制。