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Biology subjects

Musset, H.

Publications and source records attributed to Musset, H..

2 recordsLinked to original sources

A microcircuit model for initiation and reward-dependent termination of hippocampal replay

Sharp-wave ripples (SWRs) serve as a key network state in which the hippocampus replays spatiotemporal patterns that reflect animals experiences. However, how the hippocampal circuitry controls the generation, duration, and termination of these events remains unclear. To clarify how behaviorally salient locations are encoded into replay, we constructed a biologically plausible model of area CA3, including three classes of inhibitory neurons -- parvalbumin-positive basket cells, cholecystokinin-positive basket cells (CCKBC), and theta-OFF, ripple-ON cells (TORO). In our model, replay and SWRs emerge from TORO-mediated release of CCKBC inhibition onto pyramidal cells, as hypothesized by experiments. Furthermore, our model suggests that short-term depression at TORO-CCKBC synapses controls replay duration and identifies a mechanism through which replay overrepresents reward-associated locations. Our model predicts that replays terminating at these locations are shorter, which we confirm in experimental data. Overall, this study provides a mechanistic framework for SWRs and replay dynamics in the hippocampus.

neuroscience↗

Analyses of cephalic and non-cephalic sensory cell types provide insight into joint photo- and mechanoreceptor evolution

Rhabdomeric Opsins (r-Opsins) are light-sensors in cephalic eye photoreceptors, but also function in additional sensory organs. This has prompted questions on the evolutionary relationship of these cell types, and if ancient r-Opsins cells were non-photosensory. Our profiling of cephalic and non-cephalic r-opsin1-expressing cells of the marine bristleworm Platynereis dumerilii reveals shared and distinct features. Non-cephalic cells possess a full set of phototransduction components, but also a mechanosensory signature. We determine that Pdu-r-Opsin1 is a Gq-coupled blue-light receptor. Profiling of cells from r-opsin1 mutants versus wild-types, and a comparison under different light conditions reveals that in the non-cephalic cells, light - mediated by r-Opsin1 - adjusts the expression level of a calcium transporter relevant for auditory mechanosensation in vertebrates. We establish a deep learning-based quantitative behavioral analysis for animal trunk movements, and identify a light-and r-Opsin-1-dependent fine-tuning of the worms undulatory movements in headless trunks, which are known to require mechanosensory feedback. Our results suggest an evolutionary concept in which r-Opsins act as ancient, light-dependent modulators of mechanosensation, and suggest that light-independent mechanosensory roles of r-Opsins likely evolved secondarily.

developmental biology↗