2/8 We approached this question by investigating the wiring of PV+ and SST+ interneurons in the mouse neocortex. These cells have highly related developmental trajectories but play very different roles in adulthood, making them an attractive model for studying synapse specificity
3/8 We found that the mTORC1 inhibitor Tsc2 is required in PV+ but not SST+ interneurons to develop excitatory synapses targeting these cells. Notably, Tsc2 is not needed to make PV+ inhibitory output synapses: its function in this context is cell-type and synapse-type-specific.
4/8 How is this achieved? We identified a signalling pathway unique to PV+ cells that regulates the formation of the excitatory inputs they receive: Tsc2 regulation by the receptor tyrosine kinase ErbB4 enables the synthesis of specific proteins required for synapse formation.
5/8 We demonstrate that several proteins required for building excitatory synapses onto PV+ cells are synthesised locally at developing synapses. So, local translation contributes to brain wiring not only during axon guidance but also in the final stages of circuit assembly.
6/8 A fascinating finding is that many genes linked to #autism seem to be dysregulated at the synapses by the loss of ErbB4 in PV+ interneurons, suggesting that the synapses between excitatory pyramidal cells and PV+ cells are a hotspot for genetic risk factors in #ASD