Laboratory of Neuronal Signaling, Institute of Experimental Medicine, 1083, Budapest, Hungary.
Nat Commun. 2020 Mar 16;11(1):1413. doi: 10.1038/s41467-020-15147-6.
Clustering of functionally similar synapses in dendrites is thought to affect neuronal input-output transformation by triggering local nonlinearities. However, neither the in vivo impact of synaptic clusters on somatic membrane potential (sVm), nor the rules of cluster formation are elucidated. We develop a computational approach to measure the effect of functional synaptic clusters on sVm response of biophysical model CA1 and L2/3 pyramidal neurons to in vivo-like inputs. We demonstrate that small synaptic clusters appearing with random connectivity do not influence sVm. With structured connectivity, ~10-20 synapses/cluster are optimal for clustering-based tuning via state-dependent mechanisms, but larger selectivity is achieved by 2-fold potentiation of the same synapses. We further show that without nonlinear amplification of the effect of random clusters, action potential-based, global plasticity rules cannot generate functional clustering. Our results suggest that clusters likely form via local synaptic interactions, and have to be moderately large to impact sVm responses.
功能相似的突触在树突中的聚类被认为通过触发局部非线性影响神经元的输入-输出转换。然而,突触聚类对体细胞膜电位(sVm)的体内影响,以及聚类形成的规则都没有得到阐明。我们开发了一种计算方法来测量功能性突触聚类对生物物理模型 CA1 和 L2/3 锥体神经元对类似体内输入的 sVm 反应的影响。我们证明,随机连接出现的小突触聚类不会影响 sVm。在结构连接的情况下,~10-20 个突触/簇是通过状态相关机制进行基于聚类的调谐的最佳选择,但通过相同突触的两倍增强可以实现更大的选择性。我们进一步表明,如果没有随机聚类效应的非线性放大,基于动作电位的全局可塑性规则不能产生功能性聚类。我们的结果表明,聚类可能是通过局部突触相互作用形成的,并且必须足够大才能影响 sVm 反应。