Extrinsic control and intrinsic computation in the hippocampal CA1 circuit

In understanding circuit operations, a key problem is the extent to which neuronal spiking reflects local computation or responses to upstream inputs. We addressed this issue in the hippocampus by performing combined optogenetic and pharmacogenetic local and upstream inactivation. Silencing the medial entorhinal cortex (mEC) largely abolished extracellular theta and gamma currents in CA1 while only moderately affecting firing rates. In contrast, CA3 and local CA1 silencing strongly decreased firing of CA1 neurons without affecting theta currents. Each perturbation reconfigured the CA1 spatial map. However, the ability of the CA1 circuit to support place field activity persisted, maintaining the same fraction of spatially tuned place fields and reliable assembly expression as in the intact mouse. Thus, the CA1 network can induce and maintain coordinated cell assemblies with minimal reliance on its inputs, but these inputs can effectively reconfigure and assist in maintaining stability of the CA1 map.

Automated summary

The extent to which neuronal spiking reflects local computation or responses to upstream inputs in circuit operations is a key problem in understanding. By performing experiments on the hippocampus, this study revealed that silencing the medial entorhinal cortex (mEC) largely abolished theta and gamma currents in CA1, while CA3 and local CA1 silencing strongly decreased firing of CA1 neurons. Despite these perturbations, the CA1 circuit was still able to support place field activity and maintain the spatial map.