Maccaferri G, McBain C J
National Institute of Child Health and Human Development, Laboratory of Cellular and Molecular Neurophysiology, Bethesda, Maryland 20892-4495, USA.
J Neurosci. 1996 Sep 1;16(17):5334-43. doi: 10.1523/JNEUROSCI.16-17-05334.1996.
We have investigated NMDA receptor-dependent long-term potentiation (LTP) in distinct subtypes of nonpyramidal neurons of the CA1 hippocampus using induction protocols that permitted the differentiation between a direct form of LTP and plasticity resulting simply from the "passive propagation" of LTP occurring on CA1 pyramidal neurons. Two types of stratum (st.) oriens/ alveus interneurons received passive propagation of synaptic potentiation via the recurrent collaterals of CA1 pyramidal cells, but neither subtype possessed direct plasticity. In st. radiatum, two distinct classes of cells were observed: st. radiatum interneurons that showed neither direct nor propagated forms of synaptic plasticity, and "giant cells" for which EPSPs were robustly potentiated after a pairing protocol. This potentiation is similar to the LTP described in pyramidal cells, and its induction requires NMDA receptor activation. Thus, a large heterogeneity of synaptic plasticity exists in morphologically distinct neurons and suggests that complex changes in the CA1 network properties will occur after the induction of LTP.
我们使用诱导方案研究了CA1海马体非锥体神经元不同亚型中N-甲基-D-天冬氨酸(NMDA)受体依赖性长时程增强(LTP),该方案能够区分直接形式的LTP和仅由CA1锥体神经元上发生的LTP“被动传播”所导致的可塑性。两种类型的海马伞/齿状回间质神经元通过CA1锥体细胞的回返侧支接受突触增强的被动传播,但这两种亚型均不具备直接可塑性。在辐射层,观察到两类不同的细胞:既不表现出直接形式也不表现出传播形式的突触可塑性的辐射层中间神经元,以及在配对方案后其兴奋性突触后电位(EPSP)被强烈增强的“巨细胞”。这种增强类似于锥体细胞中描述的LTP,其诱导需要NMDA受体激活。因此,形态上不同的神经元中存在很大的突触可塑性异质性,这表明LTP诱导后CA1网络特性将发生复杂变化。