Nakazawa K, Mikawa S, Hashikawa T, Ito M
Laboratory for Synaptic Function, Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.
Neuron. 1995 Sep;15(3):697-709. doi: 10.1016/0896-6273(95)90157-4.
We generated a polyclonal antibody, 12P3, specifically recognizing rat AMPA-type glutamate receptor (GluR) subunits phosphorylated at Ser-696 of GluR2 or at the homologous sites in GluR1, GluR3, and GluR4. Using 12P3, we demonstrate that a brief exposure of a rat cerebellar slice to AMPA leads to transient phosphorylation of the GluR subunits in Purkinje cell dendrites. Persistent phosphorylation over 30 min was obtained when exposure to AMPA was preceded by a 15 min perfusion of the slice with 8-bromo-cGMP, dibutyryl-cGMP, or calyculin A but not phorbol 12,13-diacetate. These results indicate that Ser-696 of GluR2, or the corresponding sites in other AMPA receptor subunits, is a specific site at which phosphorylation takes place when AMPA-type GluRs are activated by agonists, especially under the influence of certain second messenger activities.
我们制备了一种多克隆抗体12P3,它能特异性识别在GluR2的Ser-696位点或GluR1、GluR3和GluR4的同源位点发生磷酸化的大鼠AMPA型谷氨酸受体(GluR)亚基。利用12P3,我们证明将大鼠小脑薄片短暂暴露于AMPA会导致浦肯野细胞树突中GluR亚基的瞬时磷酸化。当在暴露于AMPA之前用8-溴-cGMP、二丁酰-cGMP或花萼海绵诱癌素A(但不是佛波醇12,13-二乙酸酯)对薄片进行15分钟的灌注时,可获得持续30分钟以上的磷酸化。这些结果表明,GluR2的Ser-696位点或其他AMPA受体亚基中的相应位点,是AMPA型GluRs被激动剂激活时发生磷酸化的特定位点,尤其是在某些第二信使活性的影响下。