Abstract
Autapses are self-synapses formed by a single neuron. They selectively form in a subpopulation of neocortical glutamatergic pyramidal cells (PCs) where autaptic transmission provides strong feedback regulation of self-activity in individual neurons. PCs in the hippocampal formation (HPF) possess morphological and electrophysiological characteristics similar to neocortical PCs, it remains unclear, however, whether they form functional autapses. We performed whole-cell recording from HPF PCs in acute slices obtained from mice of either sex and found surprisingly that none of the recorded PCs in CA1, CA2 and CA3 show autaptic responses, only a subpopulation of PCs (∼50%) in the subiculum form functional autapses, particularly those targeting to the nucleus accumbens. Further experiments reveal that the autaptic responses in subicular PCs are mediated solely by AMPA receptors but not NMDA receptors, and occur much earlier than those of the medial prefrontal cortex (mPFC) during early development. Together, the results indicate that functional autapses selectively form in a considerable subset of subicular PCs, but are completely absent from PCs in the hippocampus proper, suggesting a key role of autapses in regulating the self-activity of subicular PCs and thus the main output signals of the hippocampus.
Significance Statement Neurons of HPF wire together through synapses to form circuits critical for high-order brain functions. Unlike conventional synapses formed by two neurons, autapses are self-synapses providing feedback regulation of a neuron’s own activity. We find that autapses selectively form in a subpopulation of subicular PCs, but are entirely absent from other HPF PCs, suggesting a key role of autapses in regulating the self-activity of individual subicular PCs and thereby the primary output of HPF. Additionally, autapses of subicular PCs emerge earlier than those in mPFC, and their time course correlates well with developmental changes in neuronal morphology. Therefore, the selective and early formation of autapses in subicular PCs may play a vital role in early-life cognitive functions.
Footnotes
The authors have no conflict of interest to declare.
This study was supported by the National Natural Science Foundation of China (NSFC) grants (32130044 and T2241002, Y.S.), STI2030-Major Projects (2021ZD0202500, Y.S.), Program of Shanghai Academic/Technology Research Leader (21XD1400100, Y.S.), and two other NSFC grants (32200953 for W.K. and 32100930 for Q.H.).