Author:
Sofroniew N. J.,Flickinger D.,King J.,Svoboda K.
Abstract
AbstractImaging is used to map activity across populations of neurons. Microscopes with cellular resolution have small (< 1 millimeter) fields of view and cannot simultaneously image activity distributed across multiple brain areas. Typical large field of view microscopes do not resolve single cells, especially in the axial dimension. We developed a 2-photon random access mesoscope (2p-RAM) that allows high-resolution imaging anywhere within a volume spanning multiple brain areas (Ø 5 mm × 1 mm cylinder). 2p-RAM resolution is near diffraction limited (lateral, 0.66 μm, axial 4.09 μm at the center; excitation wavelength = 970 nm; numerical aperture = 0.6) over a large range of excitation wavelengths. A fast threedimensional scanning system allows efficient sampling of neural activity in arbitrary regions of interest across the entire imaging volume. We illustrate the use of the 2p-RAM by imaging neural activity in multiple, non-contiguous brain areas in transgenic mice expressing protein calcium sensors.
Publisher
Cold Spring Harbor Laboratory
Reference58 articles.
1. Whole-brain functional imaging at cellular resolution using light-sheet microscopy
2. Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics;Frontiers in molecular neuroscience,2013
3. Optimization of a GCaMP Calcium Indicator for Neural Activity Imaging
4. Extremely simple single-prism ultrashort-pulse compressor;Optics express,2006
5. Born, M. and E. Wolf (1980). Principles of Optics. Oxford, Pergamon.
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献