| Literature DB >> 24920579 |
Marco Terenzio1, Matthew Golding2, Matthew R G Russell3, Krzysztof B Wicher4, Ian Rosewell5, Bradley Spencer-Dene6, David Ish-Horowicz4, Giampietro Schiavo7.
Abstract
We have identified a new function for the dynein adaptor Bicaudal D homolog 1 (BICD1) by screening a siRNA library for genes affecting the dynamics of neurotrophin receptor-containing endosomes in motor neurons (MNs). Depleting BICD1 increased the intracellular accumulation of brain-derived neurotrophic factor (BDNF)-activated TrkB and p75 neurotrophin receptor (p75(NTR)) by disrupting the endosomal sorting, reducing lysosomal degradation and increasing the co-localisation of these neurotrophin receptors with retromer-associated sorting nexin 1. The resulting re-routing of active receptors increased their recycling to the plasma membrane and altered the repertoire of signalling-competent TrkB isoforms and p75(NTR) available for ligand binding on the neuronal surface. This resulted in attenuated, but more sustained, AKT activation in response to BDNF stimulation. These data, together with our observation that Bicd1 expression is restricted to the developing nervous system when neurotrophin receptor expression peaks, indicate that BICD1 regulates neurotrophin signalling by modulating the endosomal sorting of internalised ligand-activated receptors.Entities:
Keywords: Bicd1; TrkB; intracellular sorting; neurotrophin signalling; p75NTR
Mesh:
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Year: 2014 PMID: 24920579 PMCID: PMC4198053 DOI: 10.15252/embj.201387579
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598