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Huang, H. H.- Y.

Publications and source records attributed to Huang, H. H.- Y..

2 recordsLinked to original sources

Cellular and circuit mechanisms underlying binocular vision

How binocular visual information is combined at the level of single neurons in the brain is not fully understood. Here, we show in mice that callosal input from the opposite visual cortex (V1) plays a critical role in this process. In vivo we find this callosal projection carries ipsilateral eye information and synapses exclusively onto binocular neurons. Using the presence of callosal input to identify binocular neurons in vitro, at the cellular level we show that binocular neurons are less excitable than monocular neurons due to high expression of Kv1 potassium channels. At the circuit level we find that only monocular neurons send callosal projections to the opposite V1, whereas binocular neurons do not. Finally, using dual-colour optogenetics we show that most binocular and monocular neurons receive direct input from the thalamus. In summary, we describe distinct cellular and circuit mechanisms underlying processing of binocular visual information in mouse V1.

neuroscience↗

Multi-functional feedforward inhibitory circuits for cortical odor processing

Feedforward inhibitory circuits are key contributors to the complex interplay between excitation and inhibition in the brain. Little is known about the function of feedforward inhibition in the primary olfactory (piriform) cortex. Using in vivo two-photon targeted patch clamping and calcium imaging in mice, we find that odors evoke strong excitation in two classes of interneurons - neurogliaform (NG) cells and horizontal (HZ) cells - that provide feedforward inhibition in layer 1 of the piriform cortex. NG cells fire much earlier than HZ cells following odor onset, a difference that can be attributed to the faster odor-driven excitatory synaptic drive that NG cells receive from the olfactory bulb. As a consequence, NG cells strongly but transiently inhibit odor-evoked excitation in layer 2 principal cells, whereas HZ cells provide more diffuse and prolonged feedforward inhibition. Our findings reveal unexpected complexity in the operation of inhibition in the piriform cortex.

neuroscience↗