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Updated: Feb 2, 2026

Isolation and RNA Extraction of Neurons, Macrophages and Microglia from Larval Zebrafish Brains
Published on: April 27, 2018
Whole-Brain Calcium Imaging during Physiological Vestibular Stimulation in Larval Zebrafish
Geoffrey Migault1, Thijs L van der Plas2, Hugo Trentesaux1
1Laboratoire Jean Perrin, Sorbonne Université, UMR 8237, 75005 Paris, France; Laboratoire Jean Perrin, CNRS, UMR 8237, 75005 Paris, France.
Abstract:
The vestibular apparatus provides animals with postural and movement-related information that is essential to adequately execute numerous sensorimotor tasks. In order to activate this sensory system in a physiological manner, one needs to macroscopically rotate or translate the animal's head, which in turn renders simultaneous neural recordings highly challenging. Here we report on a novel miniaturized, light-sheet microscope that can be dynamically co-rotated with a head-restrained zebrafish larva, enabling controlled vestibular stimulation. The mechanical rigidity of the microscope allows one to perform whole-brain functional imaging with state-of-the-art resolution and signal-to-noise ratio while imposing up to 25° in angular position and 6,000°/s2 in rotational acceleration. We illustrate the potential of this novel setup by producing the first whole-brain response maps to sinusoidal and stepwise vestibular stimulation. The responsive population spans multiple brain areas and displays bilateral symmetry, and its organization is highly stereotypic across individuals. Using Fourier and regression analysis, we identified three major functional clusters that exhibit well-defined phasic and tonic response patterns to vestibular stimulation. Our rotatable light-sheet microscope provides a unique tool for systematically studying vestibular processing in the vertebrate brain and extends the potential of virtual-reality systems to explore complex multisensory and motor integration during simulated 3D navigation.
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