| Literature DB >> 33878295 |
Keisuke Ota1, Yasuhiro Oisi1, Takayuki Suzuki1, Muneki Ikeda2, Yoshiki Ito3, Tsubasa Ito4, Hiroyuki Uwamori1, Kenta Kobayashi5, Midori Kobayashi1, Maya Odagawa1, Chie Matsubara1, Yoshinori Kuroiwa6, Masaru Horikoshi6, Junya Matsushita7, Hiroyuki Hioki8, Masamichi Ohkura9, Junichi Nakai10, Masafumi Oizumi11, Atsushi Miyawaki1, Toru Aonishi4, Takahiro Ode12, Masanori Murayama13.
Abstract
Fast and wide field-of-view imaging with single-cell resolution, high signal-to-noise ratio, and no optical aberrations have the potential to inspire new avenues of investigations in biology. However, such imaging is challenging because of the inevitable tradeoffs among these parameters. Here, we overcome these tradeoffs by combining a resonant scanning system, a large objective with low magnification and high numerical aperture, and highly sensitive large-aperture photodetectors. The result is a practically aberration-free, fast-scanning high optical invariant two-photon microscopy (FASHIO-2PM) that enables calcium imaging from a large network composed of ∼16,000 neurons at 7.5 Hz from a 9 mm2 contiguous image plane, including more than 10 sensory-motor and higher-order areas of the cerebral cortex in awake mice. Network analysis based on single-cell activities revealed that the brain exhibits small-world rather than scale-free behavior. The FASHIO-2PM is expected to enable studies on biological dynamics by simultaneously monitoring macroscopic activities and their compositional elements.Entities:
Keywords: in vivo calcium imaging; mouse; neocortex; network analysis; objective lense; optical invariant; resonant scanning; small-world network; two-photon microscopy; wide field-of-view
Year: 2021 PMID: 33878295 DOI: 10.1016/j.neuron.2021.03.032
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173