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Gao, W.-J.

Publications and source records attributed to Gao, W.-J..

2 recordsLinked to original sources

Gating of Memory to Behavior by the Locus Coeruleus

An essential function of memory is to guide behavior for survival and adaptation. While considerable knowledge has been accumulated on memory formation, much less is understood about how retrieved memories direct behavior/action. In the auditory Pavolovian threat conditioning paradigm, retrieval of conditioned threat memory activates dorsomedial prefrontal (dmPFC) neurons exhibiting transient responses (T-neurons), which activate both dmPFC neurons exhibiting sustained responses (S-neurons) and locus coeruleus (LC) neurons. Auditory inputs to S-neurons enable the conversion from transient to sustained responses so that the freezing durations match those of the auditory cues. Activation of LC neurons is required for the conversion by enhancing S-neuron responses, which, interestingly, opens a short time window during which non-conditioned cues also lead to freezing. The transition from memory to behavior thus hinges on the integration of retrieved memory, sensory inputs, and emotional/body state cues to generate a selective, adequate, and finely tuned behavior. Significance statementThis study provides new insights into the neural circuitry and mechanisms of how retrieved memories direct the execution of behavior in response to conditioned threatening stimuli. It reveals how different neuron types in the dmPFC interact with LC neurons to determine and modulate the duration and intensity of defensive responses. It also shows that activation of LC neurons can induce the generalization of freezing to non-threatening cues, which may have implications for understanding anxiety disorders. This study contributes to the field of neuroscience by advancing the understanding of memory-behavior conversion and role of the dmPFC and LC in conditioned threat/fear behavior.

neuroscience↗

Sonic hedgehog signaling in astrocytes mediates cell-type-specific synaptic organization

Astrocytes have emerged as integral partners with neurons in regulating synapse formation and function, but the mechanisms that mediate these interactions are not well understood. Here, we show that Sonic hedgehog (Shh) signaling between neurons and astrocytes is required for establishing structural organization and remodeling of cortical synapses in a cell type-specific manner. In the postnatal cortex, Shh signaling is active in a subpopulation of mature astrocytes localized primarily in deep cortical layers. Selective disruption of Shh signaling in astrocytes produces a dramatic increase in synapse number specifically on layer V apical dendrites that emerges during adolescence and persists into adulthood. Dynamic turnover of dendritic spines is impaired in mutant mice and is accompanied by an increase in neuronal excitability and a reduction of the glial-specific, inward-rectifying K+ channel Kir4.1. These data identify a critical role for Shh signaling in astrocyte-mediated modulation of neuronal activity required for sculpting synapses.

neuroscience↗