BDNF regulates the translation of a select group of mRNAs by a mammalian target of rapamycin-phosphatidylinositol 3-kinase-dependent pathway during neuronal development

被引:317
作者
Schratt, GM
Nigh, EA
Chen, WG
Hu, L
Greenberg, ME [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Program Biol & Biomed Sci, Boston, MA 02115 USA
[5] Childrens Hosp, Div Neurosci, Boston, MA 02115 USA
关键词
BDNF; translation; microarray; axon guidance; synaptic plasticity; rapamycin;
D O I
10.1523/JNEUROSCI.1739-04.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Local regulation of mRNA translation plays an important role in axon guidance, synaptic development, and neuronal plasticity. Little is known, however, regarding the mechanisms that control translation in neurons, and only a few mRNAs have been identified that are locally translated within axon and dendrites. Using Affymetrix gene arrays to identify mRNAs that are newly associated with polysomes after exposure to BDNF, we identified subsets of mRNAs for which translation is enhanced in neurons at different developmental stages. In mature neurons, many of these mRNAs encode proteins that are known to function at synapses, including CamKIIalpha, NMDA receptor subunits, and the postsynaptic density (PSD) scaffolding protein Homer2. BDNF regulates the translation of Homer2 locally in the synaptodendritic compartment by activating translational initiation via a mammalian target of rapamycin-phosphatidylinositol 3-kinase-dependent pathway. These findings suggest that BDNF likely regulates synaptic function by inducing the local synthesis of numerous synaptic proteins. The local translation of the cytoskeleton-associated protein Homer2 in particular might have important implications for growth cone dynamics and dendritic spine development.
引用
收藏
页码:7366 / 7377
页数:12
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