Spatially local inhibition and synaptic plasticity together enable dynamic, context-dependent integration of parallel sensory pathways.

Authors

Qiang Chen, Fred Rieke

Published in

Cell reports. Volume 45. Issue 5. Pages 117306. May 26, 2026. Epub Apr 24, 2026.

Abstract

Retinal ganglion cells have traditionally been grouped into cells that are sensitive to luminance but not spatial structure and cells with responses that are enhanced by spatial structure. Neither category describes mouse Off-transient alpha cells, which respond strongly to spatially homogeneous inputs and are suppressed by spatial structure. We identified two circuit mechanisms that together can explain this unusual spatial selectivity. First, the inhibition that controls responses of these cells is tuned to finer spatial structure than excitation, causing the balance of excitation and inhibition to depend on spatial scale. Second, the excitatory synapses onto these cells undergo strong synaptic depression, and the modulation of that depression by presynaptic inhibition amplifies responses to the transition from spatially structured to homogeneous inputs. A spatiotemporal computational model incorporating these circuit features quantitatively recapitulates the observed responses. These findings reveal how localized inhibition and short-term plasticity jointly create the distinctive spatial selectivity of Off-transient cells.

PMID:
42033725
Bibliographic data and abstract were imported from PubMed on 14 Sep 2026.

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