4.7 Article

The tyrosine kinase Fyn determines the localization of TrkB receptors in lipid rafts

Journal

JOURNAL OF NEUROSCIENCE
Volume 27, Issue 18, Pages 4859-4869

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.4587-06.2007

Keywords

TrkB; Fyn; PLC gamma; lipid rafts; intracellular; rat

Categories

Funding

  1. NICHD NIH HHS [P01 HD023315, HD23315] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS021072, R56 NS021072, NS21072] Funding Source: Medline

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Localization of Trk neurotrophin receptors is an important factor in directing cellular communication in developing and mature neurons. One potential site of action is in lipid raft membrane microdomains. Although Trk receptors have been localized to lipid rafts, little is known about how these neurotrophin receptors are directed there or how localization to these membrane microdomains regulates Trk signaling. Here, we report that the TrkB brain-derived neurotrophic factor (BDNF) receptor specifically localized to intracellular lipid rafts in cortical and hippocampal membranes in response to BDNF and that this process was critically dependent on the tyrosine kinase Fyn. BDNF-induced TrkB accumulation at lipid rafts was prevented by blocking the internalization of TrkB. BDNF stimulation also resulted in the association between endogenous TrkB and Fyn. Moreover, in neurons derived from Fyn knock-out mice, the translocation of TrkB to lipid rafts in response to BDNF was compromised, whereas the corticohippocampal region of Fyn mutants displayed lower amounts of TrkB in lipid rafts in vivo. In support of a role for lipid rafts in neurotrophin signaling, inhibiting TrkB translocation to lipid rafts, either by using Fyn knock-out neurons or lipid raft- disturbing agents, prevented the full activation of TrkB and of downstream phospholipase C-gamma. These results indicate that the lipid raft localization of TrkB receptors is regulated by Fyn and represents an important factor in determining the outcome of BDNF signaling in neurons.

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