Derkach V, Barria A, Soderling T R
Vollum Institute, Oregon Health Sciences University, Portland, OR 97201, USA.
Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):3269-74. doi: 10.1073/pnas.96.6.3269.
The ability of central glutamatergic synapses to change their strength in response to the intensity of synaptic input, which occurs, for example, in long-term potentiation (LTP), is thought to provide a cellular basis for memory formation and learning. LTP in the CA1 field of the hippocampus requires activation of Ca2+/calmodulin-kinase II (CaM-KII), which phosphorylates Ser-831 in the GluR1 subunit of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate glutamate receptor (AMPA-R), and this activation/phosphorylation is thought to be a postsynaptic mechanism in LTP. In this study, we have identified a molecular mechanism by which CaM-KII potentiates AMPA-Rs. Coexpression in HEK-293 cells of activated CaM-KII with GluR1 did not affect the glutamate affinity of the receptor, the kinetics of desensitization and recovery, channel rectification, open probability, or gating. Single-channel recordings identified multiple conductance states for GluR1, and coexpression with CaM-KII or a mutation of Ser-831 to Asp increased the contribution of the higher conductance states. These results indicate that CaM-KII can mediate plasticity at glutamatergic synapses by increasing single-channel conductance of existing functional AMPA-Rs or by recruiting new high-conductance-state AMPA-Rs.
中枢谷氨酸能突触响应突触输入强度而改变其强度的能力,例如在长时程增强(LTP)中发生的这种情况,被认为为记忆形成和学习提供了细胞基础。海马体CA1区的LTP需要激活钙/钙调蛋白依赖性蛋白激酶II(CaM-KII),其使α-氨基-3-羟基-5-甲基-4-异恶唑丙酸谷氨酸受体(AMPA-R)的GluR1亚基中的Ser-831磷酸化,并且这种激活/磷酸化被认为是LTP中的一种突触后机制。在本研究中,我们确定了一种CaM-KII增强AMPA-Rs的分子机制。在HEK-293细胞中,激活的CaM-KII与GluR1共表达并不影响受体的谷氨酸亲和力、脱敏和恢复动力学、通道整流、开放概率或门控。单通道记录确定了GluR1的多个电导状态,并且与CaM-KII共表达或将Ser-831突变为Asp会增加较高电导状态的贡献。这些结果表明,CaM-KII可以通过增加现有功能性AMPA-Rs的单通道电导或通过募集新的高电导状态的AMPA-Rs来介导谷氨酸能突触的可塑性。