Poster abstracts
Poster number 62 submitted by Meretta Hanson
Development of differential sublaminar feedforward inhibitory circuits in CA1 hippocampus requires Satb2
Meretta A. Hanson (Department of Neuroscience), Noor Bibi (Department of Neuroscience), Alireza Safa (Department of Neuroscience), Devipriyanka Nagarajan (Department of Neuroscience), Alec H. Marshall (Department of Neuroscience), Aidan C. Johantges (Department of Neuroscience)
Abstract:
Pyramidal cells (PCs) in CA1 hippocampus can be classified by their radial position as deep or superficial and organize into subtype-specific circuits necessary for differential information processing. Specifically, superficial PCs receive fewer inhibitory synapses from parvalbumin (PV)-expressing interneurons than deep PCs, resulting in weaker feedforward inhibition of input from CA3 Schaffer collaterals. Using mice, we investigated mechanisms underlying PC differentiation and the development of this inhibitory circuit motif. We found that expression of the transcriptional regulator SATB2 is biased towards superficial PCs during early postnatal development and necessary to suppress PV+ interneuron synapse formation. In the absence of SATB2, the number of PV+ interneuron synaptic puncta surrounding superficial PCs increases during development to match deep PCs. This results in equivalent inhibitory current strength observed in paired whole-cell recordings, and equivalent feedforward inhibition of Schaffer collateral input. Thus, SATB2 is necessary for superficial PC differentiation and biased feedforward inhibition in CA1.
Keywords: electrophysiology, neural circuit, development