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Updated: Mar 10, 2026

Multi-layer Cortical Ca2+ Imaging in Freely Moving Mice with Prism Probes and Miniaturized Fluorescence Microscopy
Published on: June 13, 2017
An implanted lennula approach to measure neural Ca2+ responses in the awake marmoset visual cortex
Soo Hyun Park1,2, Stephany A Nti2, Madeline Marcelle3
1Department of Brain and Cognitive Sciences, KAIST, Daejeon, Republic of Korea.
Abstract:
We present a novel approach for endoscopic calcium imaging in the marmoset extrastriate visual cortex, combining a chronically implanted microprism lens with an integrated injection cannula. This method achieved stable, longitudinal imaging of visually responsive GCaMP-expressing neurons over multiple weeks. Using a head-mounted miniscope in two subjects, we repeatedly presented naturalistic visual stimuli and longitudinally tracked the activity of more than one hundred neurons across sessions within an 800-μm2 field of view. Stably monitored neurons in cortical areas V3 and MT responded reliably to visual images and movies over periods up to 3 weeks. Cells having different visual response preferences were spatially intermixed. These results demonstrate the feasibility of longitudinal calcium imaging in the primate visual cortex using a single-surgery, integrated lens-cannula approach, and provide initial insights into single neuron response stability and diversity to naturalistic stimuli in mid-level cortical visual areas.

