| Literature DB >> 21775604 |
Shu-Hong Huang1, Shan Duan, Tao Sun, Jue Wang, Ling Zhao, Zhao Geng, Jing Yan, Hai-Ji Sun, Zhe-Yu Chen.
Abstract
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.Entities:
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Year: 2011 PMID: 21775604 PMCID: PMC6622626 DOI: 10.1523/JNEUROSCI.0436-11.2011
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167