Department of Molecular Neuroscience, Osaka University Graduate School of Medicine, Suita 565-0871, Japan, and
Department of Physiology, Faculty of Medicine, Saitama Medical University, Moroyama, Saitama 350-0495, Japan
J Neurosci. 2019 May 15;39(20):3784-3791. doi: 10.1523/JNEUROSCI.1684-18.2019. Epub 2019 Mar 15.
Spike timing is an important factor in the modification of synaptic strength. Various forms of spike timing-dependent plasticity (STDP) occur in the brains of diverse species, from insects to humans. In unimodal STDP, only LTP or LTD occurs at the synapse, regardless of which neuron spikes first; the magnitude of potentiation or depression increases as the time between presynaptic and postsynaptic spikes decreases. This from of STDP may promote developmental strengthening or weakening of early projections. In bidirectional Hebbian STDP, the magnitude and the sign (potentiation or depression) of plasticity depend, respectively, on the timing and the order of presynaptic and postsynaptic spikes. In the rodent barrel cortex, multiple forms of STDP appear sequentially during development, and they contribute to network formation, retraction, or fine-scale functional reorganization. Hebbian STDP appears at L4-L2/3 synapses starting at postnatal day (P) 15; the synapses exhibit unimodal "all-LTP STDP" before that age. The appearance of Hebbian STDP at L4-L2/3 synapses coincides with the maturation of parvalbumin-containing GABA interneurons in L4, which contributes to the generation of L4-before-L2/3 spiking in response to thalamic input by producing fast feedforward suppression of both L4 and L2/3 cells. After P15, L4-L2/3 STDP mediates fine-scale circuit refinement, essential for the critical period in the barrel cortex. In this review, we first briefly describe the relevance of STDP to map plasticity in the barrel cortex, then look over roles of distinct forms of STDP during development. Finally, we propose a hypothesis that explains the transition from network formation to the initiation of the critical period in the barrel cortex.
尖峰时间是突触强度修饰的一个重要因素。从昆虫到人类等各种物种的大脑中都存在各种形式的尖峰时间依赖性可塑性(STDP)。在单峰 STDP 中,无论哪个神经元先放电,突触处只会发生 LTD 或 LTP;随着突触前和突触后尖峰之间的时间减少,增强或抑制的幅度增加。这种形式的 STDP 可能促进早期投射的发育性增强或减弱。在双向海伯 STDP 中,可塑性的幅度和符号(增强或抑制)分别取决于突触前和突触后尖峰的时间和顺序。在啮齿动物桶状皮层中,在发育过程中会依次出现多种形式的 STDP,它们有助于网络形成、回缩或精细功能重组。在出生后第 15 天(P)开始,在 L4-L2/3 突触处出现海伯 STDP;在此之前,突触表现出单峰的“全-LTP STDP”。L4-L2/3 突触处的海伯 STDP 出现与 L4 中含有 Parvalbumin 的 GABA 中间神经元的成熟相吻合,这有助于产生 L4 比 L2/3 更早的放电,通过对 L4 和 L2/3 细胞产生快速的前馈抑制来产生对丘脑输入的反应。在 P15 之后,L4-L2/3 STDP 介导精细的电路细化,这对桶状皮层的关键期至关重要。在这篇综述中,我们首先简要描述了 STDP 与桶状皮层中地图可塑性的相关性,然后探讨了不同形式的 STDP 在发育过程中的作用。最后,我们提出了一个假设,解释了桶状皮层中从网络形成到关键期开始的转变。