| Literature DB >> 33826882 |
Michael E Xie1, Yoav Adam1, Linlin Z Fan1, Urs L Böhm1, Ian Kinsella2, Ding Zhou2, Marton Rozsa3, Amrita Singh4, Karel Svoboda3, Liam Paninski5, Adam E Cohen6.
Abstract
The ability to probe the membrane potential of multiple genetically defined neurons simultaneously would have a profound impact on neuroscience research. Genetically encoded voltage indicators are a promising tool for this purpose, and recent developments have achieved a high signal-to-noise ratio in vivo with 1-photon fluorescence imaging. However, these recordings exhibit several sources of noise and signal extraction remains a challenge. We present an improved signal extraction pipeline, spike-guided penalized matrix decomposition-nonnegative matrix factorization (SGPMD-NMF), which resolves supra- and subthreshold voltages in vivo. The method incorporates biophysical and optical constraints. We validate the pipeline with simultaneous patch-clamp and optical recordings from mouse layer 1 in vivo and with simulated and composite datasets with realistic noise. We demonstrate applications to mouse hippocampus expressing paQuasAr3-s or SomArchon1, mouse cortex expressing SomArchon1 or Voltron, and zebrafish spines expressing zArchon1.Entities:
Keywords: signal extraction; voltage imaging
Mesh:
Year: 2021 PMID: 33826882 PMCID: PMC8095336 DOI: 10.1016/j.celrep.2021.108954
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423