Early BDNF, NT-3, and NT-4 signaling events

被引:58
|
作者
Yuen, EC [1 ]
Mobley, WC
机构
[1] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[2] Stanford Univ, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
关键词
neurotrophin signaling; brain-derived neurotrophic factor; neurotrophin-3; neurotrophin-4; Trk receptor; TrkB; TrkC;
D O I
10.1006/exnr.1999.7148
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Much more is known about nerve growth factor (NGF) signaling than that initiated by brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), or NT-4. We sought to study early BDNF, NT-3, and NT-4 signaling events, Using TrkB-expressing cells, we found that BDNF and NT-4 individually induced tyrosine phosphorylation of TrkB in a dose-dependent fashion. At maximally effective concentrations, BDNF or NT-4 induced robust TrkB tyrosine phosphorylation at 5 min; this progressively declined at 15, 30, and 60 min. Using immunoprecipitation, PIS-kinase and tyrosine phosphorylated PLC-gamma 1 and SHC were shown to be associated with tyrosine phosphorylated TrkB in response to both BDNF and NT-4. BDNF and NT-4 induced similar intensities of phosphorylation of TrkB and signaling intermediates at equivalent doses. NT-3 treatment of TrkC-expressing cells induced very similar patterns for induction of TrkC tyrosine phosphorylation and recruitment of signaling intermediates. BDNF, NT-3, and NT-4 caused rapid tyrosine phosphorylation of ERK and SNT. These data suggest that the earliest signaling events for BDNF, NT-3, and NT-4 are very similar to those for NGF. (C) 1999 Academic Press.
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页码:297 / 308
页数:12
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