Abstract
The medial entorhinal cortex (MEC) contains a variety of specialized spatially-tuned neurons whose properties emerge during the third postnatal week onwards in rodents. How neuronal networks underlying the spatial firing patterns are formed is largely unknown but they are hypothesized to develop from topographic modules of synchronized neurons in superficial MEC. Here, we show that developing MEC neuronal networks in the second postnatal week are synchronously active in spatially-grouped modules. Network synchrony is intrinsic to MEC and desynchronized just prior to the emergence of spatially-tuned firing properties. The MEC network is modulated but not driven by the immature hippocampus and is tightly-coupled to neighboring neocortical networks. Unlike hippocampal networks, developing modules are dominated by glutamatergic excitation rather than GABAergic inhibition. Our results demonstrate that intrinsically synchronous modules exist in immature MEC: these may play a key role in establishing and organizing circuitry necessary for spatially-tuned firing properties of MEC neurons.
