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Steininger, V.

Publications and source records attributed to Steininger, V..

2 recordsLinked to original sources

Temporal cortex astrocytic Gi-GPCR signaling regulates learned threat responses

Astrocytes are increasingly recognized as dynamic modulators of brain circuit function, memory processing, and behavior. Emerging evidence suggests that astrocytic G-protein-coupled receptors (GPCRs) are key regulators of these processes through their influence on intracellular signaling and neuron-glia interactions. Here, we show that the repertoire of functionally expressed GPCRs in cortical astrocytes is broader than previously appreciated. Yet, how distinct GPCR pathways contribute to behavioral regulation remains unknown for most brain areas and behavioral contexts. We therefore investigated the role of astrocytic GPCR signaling in the temporal cortex, a region that integrates multimodal sensory information and learned fear associations. Using chemogenetic tools to selectively activate distinct GPCR pathways in astrocytes, we demonstrate that Gi-coupled GPCR signaling, but not Gs- or Gq-coupled signaling, enhances fear memory retrieval. In vivo fiber photometry revealed that temporal cortex astrocytes exhibit robust Ca2+ transients to neutral, conditioned auditory and aversive sensory stimuli. Notably, astrocytic Gi-GPCR activation attenuated cue-evoked Ca2+ transients during memory retrieval. Together, these findings identify astrocytic GPCR signaling as a pathway-specific regulator of fear memory retrieval and suggest that astrocytic Gi-GPCR signaling modulates the processing of sensory cues to drive defensive behavior.

neuroscience↗

A dentate gyrus-CA3 inhibitory circuit promotes evolution of hippocampal-cortical ensembles during memory consolidation

Memories encoded in the dentate gyrus (DG) - CA3 circuit of the hippocampus are routed from CA1 to anterior cingulate cortex (ACC) for consolidation. Although CA1 parvalbumin inhibitory neurons (PV INs) orchestrate hippocampal-cortical communication, we know less about CA3 PV INs or DG - CA3 principal neuron - IN circuit mechanisms that contribute to evolution of hippocampal-cortical ensembles during memory consolidation. Using viral genetics to selectively mimic and boost an endogenous learning-dependent circuit mechanism, DG cell recruitment of CA3 PV INs and feed-forward inhibition (FFI) in CA3, in combination with longitudinal in vivo calcium imaging, we demonstrate that FFI facilitates formation and maintenance of context-associated neuronal ensembles in CA1. Increasing FFI in DG - CA3 promoted context specificity of neuronal ensembles in ACC over time and enhanced long-term contextual fear memory. In vivo LFP recordings in mice with increased FFI in DG - CA3 identified enhanced CA1 sharp-wave ripple - ACC spindle coupling as a potential network mechanism facilitating memory consolidation. Our findings illuminate how FFI in DG - CA3 dictates evolution of ensemble properties in CA1 and ACC during memory consolidation and suggest a teacher-like function for hippocampal CA1 in stabilization and re-organization of cortical representations.

neuroscience↗