Department of Synapses - Circuits - Plasticity, Max Planck Institute of Neurobiology, Am Klopferspitz 18, 82152 Martinsried, Germany.
Department of Synapses - Circuits - Plasticity, Max Planck Institute of Neurobiology, Am Klopferspitz 18, 82152 Martinsried, Germany.
Neuron. 2014 Apr 16;82(2):430-43. doi: 10.1016/j.neuron.2014.02.031.
Subsynaptic structures such as bouton, active zone, postsynaptic density (PSD) and dendritic spine, are highly correlated in their dimensions and also correlate with synapse strength. Why this is so and how such correlations are maintained during synaptic plasticity remains poorly understood. We induced spine enlargement by two-photon glutamate uncaging and examined the relationship between spine, PSD, and bouton size by two-photon time-lapse imaging and electron microscopy. In enlarged spines the PSD-associated protein Homer1c increased rapidly, whereas the PSD protein PSD-95 increased with a delay and only in cases of persistent spine enlargement. In the case of nonpersistent spine enlargement, the PSD proteins remained unchanged or returned to their original level. The ultrastructure at persistently enlarged spines displayed matching dimensions of spine, PSD, and bouton, indicating their correlated enlargement. This supports a model in which balancing of synaptic structures is a hallmark for the stabilization of structural modifications during synaptic plasticity.
突触下结构,如棘突、活性区、突触后密度(PSD)和树突棘,在其尺寸上高度相关,并且与突触强度相关。为什么会这样,以及在突触可塑性过程中如何维持这种相关性,目前仍知之甚少。我们通过双光子谷氨酸光解诱导棘突增大,并通过双光子延时成像和电子显微镜检查棘突、PSD 和棘突大小之间的关系。在增大的棘突中,PSD 相关蛋白 Homer1c 迅速增加,而 PSD 蛋白 PSD-95 则延迟增加,并且仅在棘突持续增大的情况下增加。在非持续棘突增大的情况下,PSD 蛋白保持不变或恢复到原来的水平。在持续增大的棘突的超微结构中显示出棘突、PSD 和棘突的匹配尺寸,表明它们的相关性增大。这支持了这样一种模型,即突触结构的平衡是在突触可塑性过程中稳定结构修饰的标志。