Scholl Benjamin, Thomas Connon I, Ryan Melissa A, Kamasawa Naomi, Fitzpatrick David
Functional Architecture and Development of Cerebral Cortex, Max Planck Florida Institute for Neuroscience, Jupiter, FL, USA.
Department of Neuroscience, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Nature. 2021 Feb;590(7844):111-114. doi: 10.1038/s41586-020-03044-3. Epub 2020 Dec 16.
Single neocortical neurons are driven by populations of excitatory inputs, which form the basis of neuronal selectivity to features of sensory input. Excitatory connections are thought to mature during development through activity-dependent Hebbian plasticity, whereby similarity between presynaptic and postsynaptic activity selectively strengthens some synapses and weakens others. Evidence in support of this process includes measurements of synaptic ultrastructure and in vitro and in vivo physiology and imaging studies. These corroborating lines of evidence lead to the prediction that a small number of strong synaptic inputs drive neuronal selectivity, whereas weak synaptic inputs are less correlated with the somatic output and modulate activity overall. Supporting evidence from cortical circuits, however, has been limited to measurements of neighbouring, connected cell pairs, raising the question of whether this prediction holds for a broad range of synapses converging onto cortical neurons. Here we measure the strengths of functionally characterized excitatory inputs contacting single pyramidal neurons in ferret primary visual cortex (V1) by combining in vivo two-photon synaptic imaging and post hoc electron microscopy. Using electron microscopy reconstruction of individual synapses as a metric of strength, we find no evidence that strong synapses have a predominant role in the selectivity of cortical neuron responses to visual stimuli. Instead, selectivity appears to arise from the total number of synapses activated by different stimuli. Moreover, spatial clustering of co-active inputs appears to be reserved for weaker synapses, enhancing the contribution of weak synapses to somatic responses. Our results challenge the role of Hebbian mechanisms in shaping neuronal selectivity in cortical circuits, and suggest that selectivity reflects the co-activation of large populations of presynaptic neurons with similar properties and a mixture of strengths.
单个新皮层神经元由兴奋性输入群体驱动,这些兴奋性输入构成了神经元对感觉输入特征选择性的基础。兴奋性连接被认为在发育过程中通过依赖活动的赫布可塑性而成熟,即突触前和突触后活动之间的相似性选择性地增强一些突触并削弱其他突触。支持这一过程的证据包括突触超微结构的测量以及体外和体内生理学及成像研究。这些相互印证的证据线索导致这样的预测:少数强突触输入驱动神经元选择性,而弱突触输入与体细胞输出的相关性较小,并整体调节活动。然而,来自皮质回路的支持证据仅限于对相邻连接细胞对的测量,这就提出了一个问题,即这一预测是否适用于汇聚到皮质神经元上的广泛突触。在这里,我们通过结合体内双光子突触成像和事后电子显微镜测量,来测量接触雪貂初级视觉皮层(V1)中单个锥体神经元的功能特征性兴奋性输入的强度。使用单个突触的电子显微镜重建作为强度指标,我们没有发现证据表明强突触在皮质神经元对视觉刺激的选择性中起主要作用。相反,选择性似乎源于不同刺激激活的突触总数。此外,共同激活输入的空间聚类似乎保留给较弱的突触,增强了弱突触对体细胞反应的贡献。我们的结果挑战了赫布机制在塑造皮质回路中神经元选择性方面的作用,并表明选择性反映了大量具有相似特性和不同强度混合的突触前神经元的共同激活。