| RRC ID |
85739
|
| Author |
Brown ST, Holla MR, Land MA, Yang S, McDonald AJ, St-Pierre F, Raman IM.
|
| Title |
High-speed voltage imaging of action potentials in molecular layer interneurons reveals sensory-driven synchrony that augments movement.
|
| Journal |
Cell Rep
|
| Abstract |
Testing whether the synchrony of action potential firing is a cerebellar coding mechanism requires simultaneous recording, with high temporal fidelity, from populations of identified neurons. Here, we used targeted one-photon voltage imaging at 2-4 kHz to record action potentials from groups of ∼10-300 molecular layer interneurons (MLIs) expressing a positively tuned, genetically encoded voltage indicator, FORCE1f or pAce. In awake resting mice, crus I MLIs fired brief (∼1-ms) spikes at 20-60 spikes/s. Sensory stimuli of air puffs to the whiskers evoked short-latency (<10 ms) increases in spiking probability. In most trials, >50% of MLIs fired synchronously with 4-ms temporal precision. The magnitude of puff-evoked whisks correlated tightly with the trial-by-trial percentage of synchrony. Brief optogenetic stimulation of MLIs was sufficient to induce and augment whisker protraction, whereas overriding MLI inhibition by stimulating target Purkinje cells reduced protractions, providing direct evidence that sensory-evoked spike synchrony can generate movement.
|
| Volume |
44(8)
|
| Pages |
116148
|
| Published |
2025-8-26
|
| DOI |
10.1016/j.celrep.2025.116148
|
| PII |
S2211-1247(25)00919-2
|
| PMID |
40811060
|
| MeSH |
Action Potentials* / physiology
Animals
Interneurons* / physiology
Male
Mice
Mice, Inbred C57BL
Movement / physiology
Optogenetics
Purkinje Cells / physiology
Vibrissae / physiology
|
| IF |
8.109
|
| Resource |
| Mice |
RBRC10109 |
