Larsen Rylan S, Smith Ikuko T, Miriyala Jayalakshmi, Han Ji Eun, Corlew Rebekah J, Smith Spencer L, Philpot Benjamin D
Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, USA.
UNC Neuroscience Center, University of North Carolina, Chapel Hill, NC 27599, USA.
Neuron. 2014 Aug 20;83(4):879-93. doi: 10.1016/j.neuron.2014.07.039.
Sensory experience orchestrates the development of cortical circuitry by adaptively modifying neurotransmission and synaptic connectivity. However, the mechanisms underlying these experience-dependent modifications remain elusive. Here we demonstrate that visual experience suppresses a presynaptic NMDA receptor (preNMDAR)-mediated form of timing-dependent long-term depression (tLTD) at visual cortex layer (L) 4-2/3 synapses. This tLTD can be maintained during development, or reinstated in adulthood, by sensory deprivation. The changes in tLTD are mirrored by changes in glutamate release; visual deprivation enhances both tLTD and glutamate release. These effects require the GluN3A NMDAR subunit, the levels of which are increased by visual deprivation. Further, by coupling the pathway-specific optogenetic induction of tLTD with cell-type-specific NMDAR deletion, we find that visual experience modifies preNMDAR-mediated plasticity specifically at L4-L2/3 synapses.
感觉经验通过适应性地改变神经传递和突触连接来协调皮质回路的发育。然而,这些依赖于经验的修饰背后的机制仍然难以捉摸。在这里,我们证明视觉经验会抑制视觉皮层第4层到第2/3层突触处由突触前NMDA受体(preNMDAR)介导的一种依赖时间的长时程抑制(tLTD)形式。这种tLTD在发育过程中可以维持,或者在成年后通过感觉剥夺恢复。tLTD的变化与谷氨酸释放的变化相对应;视觉剥夺会增强tLTD和谷氨酸释放。这些效应需要GluN3A NMDAR亚基,其水平会因视觉剥夺而增加。此外,通过将tLTD的通路特异性光遗传学诱导与细胞类型特异性NMDAR缺失相结合,我们发现视觉经验特别在第4层到第2/3层突触处修饰了preNMDAR介导的可塑性。