Laboratory of Neurobiology, Nencki-EMBL Center of Excellence for Neural Plasticity and Brain Disorders: BRAINCITY, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw 02-093, Poland.
Laboratory of Molecular Basis of Behavior, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw 02-093, Poland.
Cereb Cortex. 2021 Jul 5;31(8):3804-3819. doi: 10.1093/cercor/bhab050.
Information coding in the hippocampus relies on the interplay between various neuronal ensembles. We discovered that the application of a cholinergic agonist, carbachol (Cch), which triggers oscillatory activity in the gamma range, induces the activity of matrix metalloproteinase 9 (MMP-9)-an enzyme necessary for the maintenance of synaptic plasticity. Using electrophysiological recordings in hippocampal organotypic slices, we show that Cch potentiates the frequency of miniature inhibitory and excitatory postsynaptic currents (mIPSCs and mEPSCs, respectively) in CA1 neurons and this effect is MMP-9 dependent. Interestingly, though MMP-9 inhibition prevents the potentiation of inhibitory events, it further boosts the frequency of excitatory mEPSCs. Such enhancement of the frequency of excitatory events is a result of increased synaptogenesis onto CA1 neurons. Thus, the function of MMP-9 in cholinergically induced plasticity in the hippocampus is to maintain the fine-tuned balance between the excitatory and the inhibitory synaptic transmission.
信息在海马体中的编码依赖于各种神经元集合体的相互作用。我们发现,应用一种胆碱能激动剂,即卡巴胆碱(Cch),它可以引发γ范围内的振荡活动,诱导基质金属蛋白酶 9(MMP-9)的活性——这种酶对于维持突触可塑性是必需的。我们通过在海马体器官型切片上进行电生理记录,表明 Cch 可以增强 CA1 神经元中小抑制性和兴奋性突触后电流(mIPSCs 和 mEPSCs,分别)的频率,这种效应依赖于 MMP-9。有趣的是,尽管 MMP-9 抑制阻止了抑制性事件的增强,但它进一步增加了兴奋性 mEPSCs 的频率。这种兴奋性事件频率的增强是由于 CA1 神经元上的突触发生增加所致。因此,MMP-9 在海马体胆碱能诱导可塑性中的功能是维持兴奋性和抑制性突触传递之间的精细平衡。