| Literature DB >> 31080068 |
Masatoshi Inoue1, Atsuya Takeuchi2, Satoshi Manita3, Shin-Ichiro Horigane4, Masayuki Sakamoto5, Ryosuke Kawakami6, Kazushi Yamaguchi7, Kouhei Otomo7, Hiroyuki Yokoyama8, Ryang Kim5, Tatsushi Yokoyama5, Sayaka Takemoto-Kimura9, Manabu Abe10, Michiko Okamura5, Yayoi Kondo5, Sean Quirin11, Charu Ramakrishnan11, Takeshi Imamura12, Kenji Sakimura10, Tomomi Nemoto13, Masanobu Kano14, Hajime Fujii5, Karl Deisseroth11, Kazuo Kitamura15, Haruhiko Bito16.
Abstract
To decipher dynamic brain information processing, current genetically encoded calcium indicators (GECIs) are limited in single action potential (AP) detection speed, combinatorial spectral compatibility, and two-photon imaging depth. To address this, here, we rationally engineered a next-generation quadricolor GECI suite, XCaMPs. Single AP detection was achieved within 3-10 ms of spike onset, enabling measurements of fast-spike trains in parvalbumin (PV)-positive interneurons in the barrel cortex in vivo and recording three distinct (two inhibitory and one excitatory) ensembles during pre-motion activity in freely moving mice. In vivo paired recording of pre- and postsynaptic firing revealed spatiotemporal constraints of dendritic inhibition in layer 1 in vivo, between axons of somatostatin (SST)-positive interneurons and apical tufts dendrites of excitatory pyramidal neurons. Finally, non-invasive, subcortical imaging using red XCaMP-R uncovered somatosensation-evoked persistent activity in hippocampal CA1 neurons. Thus, the XCaMPs offer a critical enhancement of solution space in studies of complex neuronal circuit dynamics. VIDEO ABSTRACT.Entities:
Keywords: PV recording; XCaMP; ckkap sequence; genetically encoded calcium indicators; multiplex imaging; non-invasive hippocampal recording; paired pre- and post-synapse recording; two-photon Ca(2+) imaging
Mesh:
Year: 2019 PMID: 31080068 DOI: 10.1016/j.cell.2019.04.007
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582