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Elbaum, L.

Publications and source records attributed to Elbaum, L..

2 recordsLinked to original sources

Adolescent-like Processing of Behaviorally Salient Cues in Sensory and Prefrontal Cortices of Adult Preterm-Born Mice

Preterm birth is a leading risk factor for atypicalities in cognitive and sensory processing, but it is unclear how prematurity impacts circuits that support these functions. To address this, we trained adult male and female mice born a day early (preterm mice) on a visual discrimination task and found that they fail to achieve high levels of performance due to increased responding to the non-rewarded cue (false alarms). While the representation of task cues measured with in vivo electrophysiology is intact in the primary visual cortex (V1) of trained preterm mice, the representation of the non-rewarded cue is significantly weaker in regular spiking, putative pyramidal neurons in the prefrontal cortex (PFC), a brain area that mediates response inhibition. Responses to both task cues are blunted in electrophysiologically and optogenetically identified fast-spiking Parvalbumin interneurons in preterm mice, indicating impaired processing of task cues in their PFC. Indeed, single trial neuronal responses evoked by the non-rewarded cue predict the behavioral outcome more accurately in term than in preterm mice. Similar cue representation and processing is present in the PFC of adolescent term-born mice, suggesting that preterm birth impedes prefrontal maturation. Surprisingly, environmental enrichment, a well-established paradigm that promotes sensory maturation, fails to improve the performance of preterm mice. Altogether, our study describes the long-term impact of preterm birth on prefrontal and visual circuits and suggests a limited capacity of early interventions for reducing the risk of cognitive deficits after preterm birth.

neuroscience↗

Revealing Acute Consequences of Rapid Protein Elimination at Individual Synapses using Auxin-Inducible Degron 2 Technology

A powerful approach to assess a protein of interest (POI) function is its specific elimination. Common knock-out and knock-down strategies, however, are protracted and often irreversible, challenging the assessment of acute or temporary consequences in the same cells and tissues. Here we describe the use of Auxin-Inducible Degron 2 (AID2) technology to study the real-time consequences of acute POI elimination in nerve cell synapses. We demonstrate its capacity in cultured neurons and in vivo to rapidly eliminate postsynaptic scaffold proteins fused at N-terminal, C-terminal, or nested sites to GFP derivatives or HaloTag. We show that acute PSD-95 or gephyrin elimination leads to the concomitant loss of AMPA or GABAA receptors at the same synapses, and that, surprisingly, acute GKAP, but not PSD-95 elimination reduces postsynaptic scaffold size. Our findings highlight the utility of AID2 technology for rapidly eliminating synaptic POIs and studying real-time consequences in the same neurons and synapses.

neuroscience↗