Fast-spiking interneuron detonation drives high-fidelity inhibition in the olfactory bulb.
Shawn D BurtonChristina M MalyshkoNathaniel N UrbanPublished in: bioRxiv : the preprint server for biology (2024)
Inhibitory circuits in the mammalian olfactory bulb (OB) dynamically reformat olfactory information as it propagates from peripheral receptors to downstream cortex. To gain mechanistic insight into how specific OB interneuron types support this sensory processing, we examine unitary synaptic interactions between excitatory mitral and tufted cells (MTCs), the OB projection cells, and a conserved population of anaxonic external plexiform layer interneurons (EPL-INs) using pair and quartet whole-cell recordings in acute mouse brain slices. Physiological, morphological, neurochemical, and synaptic analyses divide EPL-INs into distinct subtypes and reveal that parvalbumin-expressing fast-spiking EPL-INs (FSIs) perisomatically innervate MTCs with release-competent dendrites and synaptically detonate to mediate fast, short-latency recurrent and lateral inhibition. Sparse MTC synchronization supralinearly increases this high-fidelity inhibition, while sensory afferent activation combined with single-cell silencing reveals that individual FSIs account for a substantial fraction of total network-driven MTC lateral inhibition. OB output is thus powerfully shaped by detonation-driven high-fidelity perisomatic inhibition.
Keyphrases
- single cell
- induced apoptosis
- cell cycle arrest
- mitral valve
- healthcare
- gene expression
- transcription factor
- stem cells
- heart failure
- computed tomography
- oxidative stress
- endoplasmic reticulum stress
- high throughput
- signaling pathway
- magnetic resonance imaging
- cell death
- bone marrow
- atrial fibrillation
- drug induced
- acute respiratory distress syndrome
- prefrontal cortex
- contrast enhanced
- pi k akt