Article ID Journal Published Year Pages File Type
4320772 Neuron 2016 16 Pages PDF
Abstract

•Two-photon microscope with an SLM module for fast, flexible beam redirection•Flexibly controlled, multiple-field-of-view functional imaging•Constrained nonnegative source separation algorithm to separate signals from multiple regions•Simultaneous multilayer functional in vivo imaging in the mouse cortex

SummaryRecording the activity of large populations of neurons is an important step toward understanding the emergent function of neural circuits. Here we present a simple holographic method to simultaneously perform two-photon calcium imaging of neuronal populations across multiple areas and layers of mouse cortex in vivo. We use prior knowledge of neuronal locations, activity sparsity, and a constrained nonnegative matrix factorization algorithm to extract signals from neurons imaged simultaneously and located in different focal planes or fields of view. Our laser multiplexing approach is simple and fast, and could be used as a general method to image the activity of neural circuits in three dimensions across multiple areas in the brain.

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