Liao D, Hessler N A, Malinow R
Cold Spring Harbor Laboratory, New York 11724, USA.
Nature. 1995 Jun 1;375(6530):400-4. doi: 10.1038/375400a0.
Long-term potentiation (LTP) is an enhancement of synaptic strength that can be produced by pairing of presynaptic activity with postsynaptic depolarization. LTP in the hippocampus has been extensively studied as a cellular model of learning and memory, but the nature of the underlying synaptic modification remains elusive, partly because our knowledge of central synapses is still limited. One proposal is that the modification is postsynaptic, and that synapses expressing only NMDA (N-methyl-D-aspartate) receptors before potentiation are induced by LTP to express functional AMPA (alpha-amino-3-hydroxy-5-methyl-4-isoxazoleproprionate) receptors. Here we report that a high proportion of synapses in hippocampal area CA1 transmit with NMDA receptors but not AMPA receptors, making these synapses effectively non-functional at normal resting potentials. These silent synapses acquire AMPA-type responses following LTP induction. Our findings challenge the view that LTP in CA1 involves a presynaptic modification, and suggest instead a simple postsynaptic mechanism for both induction and expression of LTP.
长时程增强(LTP)是突触强度的增强,它可通过突触前活动与突触后去极化配对产生。海马体中的LTP作为学习和记忆的细胞模型已被广泛研究,但潜在突触修饰的本质仍然难以捉摸,部分原因是我们对中枢突触的了解仍然有限。一种观点认为,这种修饰是突触后性的,并且在增强之前仅表达NMDA(N-甲基-D-天冬氨酸)受体的突触被LTP诱导表达功能性AMPA(α-氨基-3-羟基-5-甲基-4-异恶唑丙酸)受体。我们在此报告,海马体CA1区中很大一部分突触通过NMDA受体而非AMPA受体传递信息,这使得这些突触在正常静息电位下实际上不起作用。这些沉默突触在LTP诱导后获得AMPA型反应。我们的发现挑战了CA1区LTP涉及突触前修饰的观点,而是提出了一种关于LTP诱导和表达的简单突触后机制。