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Saraf-Sinik, I.

Publications and source records attributed to Saraf-Sinik, I..

3 recordsLinked to original sources

Object detection through dynamic motor-sensory convergence

To interact effectively with the world, animals coordinate how they move and how they sense. In natural settings, perceivers adapt their motor-sensory strategies as they approach and explore objects, dynamically shaping both the generation and interpretation of sensory cues. Previous attempts to explain this process by reducing it solely to neuronal representations have failed to capture the mechanisms underlying dynamic perception. In this study, we use precise behavioral tracking to investigate the initial phase of object interaction, asking: What motor-sensory strategies support object detection during natural approach? Using high resolution video tracking of rats freely exploring objects under infrared illumination, we analyzed how head and whisker dynamics evolved across sequential contacts. We found that whisker-object interactions converged toward a distinct line, *, within a motor-sensory plane, where small changes in voluntary whisker movements produced large changes in whisker curvature, a sensory correlate of contact force. This convergence was actively controlled, predicted head movements and marked the completion of object approach. Convergence to * was consistent across different objects, suggesting it serves as an invariant motor-sensory contingency for object detection. Proximity to *predicted the emergence of touch-induced pumps, a rapid motor-sensory reflex that further facilitated convergence within a single whisking cycle. Together, these results reveal that object detection is a closed-loop dynamic process, in which animals actively steer motor-sensory dynamics toward a robust detection-optimized state.

animal behavior and cognition↗

A bistable inhibitory OptoGPCR for multiplexed optogenetic control of neural circuits

Information is transmitted between brain regions through the release of neurotransmitters from long-range projecting axons. Understanding how the activity of such long-range connections contributes to behavior requires efficient methods for reversibly manipulating their function. Chemogenetic and optogenetic tools, acting through endogenous G-protein coupled receptor (GPCRs) pathways, can be used to modulate synaptic transmission, but existing tools are limited in sensitivity, spatiotemporal precision, or spectral multiplexing capabilities. Here we systematically evaluated multiple bistable opsins for optogenetic applications and found that the Platynereis dumerilii ciliary opsin (PdCO) is an efficient, versatile, light-activated bistable GPCR that can suppress synaptic transmission in mammalian neurons with high temporal precision in-vivo. PdCO has superior biophysical properties that enable spectral multiplexing with other optogenetic actuators and reporters. We demonstrate that PdCO can be used to conduct reversible loss-of-function experiments in long-range projections of behaving animals, thereby enabling detailed synapse-specific functional circuit mapping.

neuroscience↗

Optogenetic silencing of neurotransmitter release with a naturally occurring invertebrate rhodopsin

Information is carried between brain regions through neurotransmitter release from axonal presynaptic terminals. Understanding the functional roles of defined neuronal projection pathways in cognitive and behavioral processes requires temporally precise manipulation of their activity in vivo. However, existing optogenetic tools have low efficacy and off-target effects when applied to presynaptic terminals, while chemogenetic tools are difficult to control in space and time. Here, we show that a targeting-enhanced mosquito homologue of the vertebrate encephalopsin (eOPN3) can effectively suppress synaptic transmission through the Gi/o signaling pathway. Brief illumination of presynaptic terminals expressing eOPN3 triggers a lasting suppression of synaptic output that recovers spontaneously within minutes in vitro as well as in vivo. In freely moving mice, eOPN3-mediated suppression of dopaminergic nigrostriatal afferents leads to an ipsiversive rotational bias. We conclude that eOPN3 can be used to selectively suppress neurotransmitter release at synaptic terminals with high spatiotemporal precision, opening new avenues for functional interrogation of long-range neuronal circuits in vivo.

neuroscience↗