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Precision Calcium Imaging of Dense Neural Populations via a Cell-Body-Targeted Calcium Indicator.


ABSTRACT: Methods for one-photon fluorescent imaging of calcium dynamics can capture the activity of hundreds of neurons across large fields of view at a low equipment complexity and cost. In contrast to two-photon methods, however, one-photon methods suffer from higher levels of crosstalk from neuropil, resulting in a decreased signal-to-noise ratio and artifactual correlations of neural activity. We address this problem by engineering cell-body-targeted variants of the fluorescent calcium indicators GCaMP6f and GCaMP7f. We screened fusions of GCaMP to natural, as well as artificial, peptides and identified fusions that localized GCaMP to within 50 μm of the cell body of neurons in mice and larval zebrafish. One-photon imaging of soma-targeted GCaMP in dense neural circuits reported fewer artifactual spikes from neuropil, an increased signal-to-noise ratio, and decreased artifactual correlation across neurons. Thus, soma-targeting of fluorescent calcium indicators facilitates usage of simple, powerful, one-photon methods for imaging neural calcium dynamics.

SUBMITTER: Shemesh OA 

PROVIDER: S-EPMC7415598 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Precision Calcium Imaging of Dense Neural Populations via a Cell-Body-Targeted Calcium Indicator.

Shemesh Or A OA   Linghu Changyang C   Piatkevich Kiryl D KD   Goodwin Daniel D   Celiker Orhan Tunc OT   Gritton Howard J HJ   Romano Michael F MF   Gao Ruixuan R   Yu Chih-Chieh Jay CJ   Tseng Hua-An HA   Bensussen Seth S   Narayan Sujatha S   Yang Chao-Tsung CT   Freifeld Limor L   Siciliano Cody A CA   Gupta Ishan I   Wang Joyce J   Pak Nikita N   Yoon Young-Gyu YG   Ullmann Jeremy F P JFP   Guner-Ataman Burcu B   Noamany Habiba H   Sheinkopf Zoe R ZR   Park Won Min WM   Asano Shoh S   Keating Amy E AE   Trimmer James S JS   Reimer Jacob J   Tolias Andreas S AS   Bear Mark F MF   Tye Kay M KM   Han Xue X   Ahrens Misha B MB   Boyden Edward S ES  

Neuron 20200626 3


Methods for one-photon fluorescent imaging of calcium dynamics can capture the activity of hundreds of neurons across large fields of view at a low equipment complexity and cost. In contrast to two-photon methods, however, one-photon methods suffer from higher levels of crosstalk from neuropil, resulting in a decreased signal-to-noise ratio and artifactual correlations of neural activity. We address this problem by engineering cell-body-targeted variants of the fluorescent calcium indicators GCa  ...[more]

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