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Anatomical identification of extracellularly recorded cells in large-scale multielectrode recordings.
Li, Peter H; Gauthier, Jeffrey L; Schiff, Max; Sher, Alexander; Ahn, Daniel; Field, Greg D; Greschner, Martin; Callaway, Edward M; Litke, Alan M; Chichilnisky, E J.
Afiliação
  • Li PH; Departments of Neurosurgery and Ophthalmology, and Hansen Experimental Physics Laboratory, Stanford University, Stanford, California 94305, Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037, Google Inc, Mountain View, California 94043.
  • Gauthier JL; Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037.
  • Schiff M; Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037.
  • Sher A; Santa Cruz Institute for Particle Physics, University of California, Santa Cruz, California 95064.
  • Ahn D; Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037.
  • Field GD; Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037, Department of Neurobiology, Duke University School of Medicine, Durham, North Carolina 27710, and.
  • Greschner M; Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037, Department of Neuroscience, Carl von Ossietzky University, Oldenburg 26129, Germany.
  • Callaway EM; Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037.
  • Litke AM; Santa Cruz Institute for Particle Physics, University of California, Santa Cruz, California 95064.
  • Chichilnisky EJ; Departments of Neurosurgery and Ophthalmology, and Hansen Experimental Physics Laboratory, Stanford University, Stanford, California 94305, Systems Neurobiology, The Salk Institute for Biological Studies, La Jolla, California 92037, ej@stanford.edu.
J Neurosci ; 35(11): 4663-75, 2015 Mar 18.
Article em En | MEDLINE | ID: mdl-25788683
ABSTRACT
This study combines for the first time two major approaches to understanding the function and structure of neural circuits large-scale multielectrode recordings, and confocal imaging of labeled neurons. To achieve this end, we develop a novel approach to the central problem of anatomically identifying recorded cells, based on the electrical image the spatiotemporal pattern of voltage deflections induced by spikes on a large-scale, high-density multielectrode array. Recordings were performed from identified ganglion cell types in the macaque retina. Anatomical images of cells in the same preparation were obtained using virally transfected fluorescent labeling or by immunolabeling after fixation. The electrical image was then used to locate recorded cell somas, axon initial segments, and axon trajectories, and these signatures were used to identify recorded cells. Comparison of anatomical and physiological measurements permitted visualization and physiological characterization of numerically dominant ganglion cell types with high efficiency in a single preparation.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Retina / Potenciais de Ação / Líquido Extracelular Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Retina / Potenciais de Ação / Líquido Extracelular Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Neurosci Ano de publicação: 2015 Tipo de documento: Article