AMPA receptor-PDZ interactions in facilitation of spinal sensory synapses

被引:157
作者
Li, P
Kerchner, GA
Sala, C
Wei, F
Huettner, JE
Sheng, M
Zhuo, M
机构
[1] Washington Univ, Sch Med, Dept Anesthesiol Anat & Neurobiol, St Louis, MO 63110 USA
[2] Howard Hughes Med Inst, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Neurobiol, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA 02114 USA
[5] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
关键词
D O I
10.1038/14771
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Silent synapses form between some primary sensory afferents and dorsal horn neurons in the spinal cord. Molecular mechanisms for activation or conversion of silent synapses to conducting synapses are unknown. Serotonin can trigger activation of silent synapses in dorsal horn neurons by recruiting AMPA receptors. AMPA-receptor subunits GluR2 and GluR3 interact via their cytoplasmic C termini with PDZ-domain-containing proteins such as GRIP (glutamate receptor interacting protein), but the functional significance of these interactions is unclear. Here we demonstrate that protein interactions involving the GluR2/3 C terminus are important for serotonin-induced activation of silent synapses in the spinal cord. Furthermore, PKC is a necessary and sufficient trigger for this activation. These results implicate AMPA receptor-PDZ interactions in mechanisms underlying sensory synaptic potentiation and provide insights into the pathogenesis of chronic pain.
引用
收藏
页码:972 / 977
页数:6
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