Abstract
The barrel cortex (BC) processes complex direction-, frequency-, and phase-dependent input from whiskers to analyze objects in the immediate environment. Little is known about how BC microcircuits process this information and integrate input from multiple whiskers. To investigate these circuits we targeted a hybrid voltage sensor (hVOS) to Scnn1a excitatory neurons in cortical layer 4 (L4), and imaged population responses to electrical stimulation. BC in coronal and sagittal slices presented the laminar structure of the cortex with barrels aligned along stereotyped whisking directions. Voltage imaging tracked activity along an L4→L2/3→L4 relay during inter-barrel communication. AMPA receptor blockade demonstrated that this relay depends on excitatory synaptic transmission, and revealed intra- and inter-barrel feedforward inhibition. Communication between barrels was isotropic in response amplitude, half-width, and conduction velocity, but latency was longer for communication to caudal barrels. Furthermore, paired-pulse depression was weakest and recovery slowest for protraction-related directions, especially to caudally adjacent barrels. Such biases will preferentially enhance repetitive inputs in this direction. These results identify direction-dependent synaptic circuitry that shapes inter-barrel communication. Anisotropy in short-term plasticity aligns with whisker motion kinematics, suggesting that BC microcircuits are tuned to preserve temporal fidelity and selectively filter inputs according to whisking phase and direction.