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Population imaging of neural activity in awake behaving mice.
Piatkevich, Kiryl D; Bensussen, Seth; Tseng, Hua-An; Shroff, Sanaya N; Lopez-Huerta, Violeta Gisselle; Park, Demian; Jung, Erica E; Shemesh, Or A; Straub, Christoph; Gritton, Howard J; Romano, Michael F; Costa, Emma; Sabatini, Bernardo L; Fu, Zhanyan; Boyden, Edward S; Han, Xue.
Afiliação
  • Piatkevich KD; Media Lab, MIT, Cambridge, MA, USA.
  • Bensussen S; MIT McGovern Institute for Brain Research, MIT, Cambridge, MA, USA.
  • Tseng HA; Department of Biomedical Engineering, Boston University, Boston, MA, USA.
  • Shroff SN; Department of Biomedical Engineering, Boston University, Boston, MA, USA.
  • Lopez-Huerta VG; Department of Biomedical Engineering, Boston University, Boston, MA, USA.
  • Park D; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Jung EE; Media Lab, MIT, Cambridge, MA, USA.
  • Shemesh OA; MIT McGovern Institute for Brain Research, MIT, Cambridge, MA, USA.
  • Straub C; Media Lab, MIT, Cambridge, MA, USA.
  • Gritton HJ; Department of Mechanical and Industrial Engineering, University of Illinois, Chicago, IL, USA.
  • Romano MF; Media Lab, MIT, Cambridge, MA, USA.
  • Costa E; MIT McGovern Institute for Brain Research, MIT, Cambridge, MA, USA.
  • Sabatini BL; Howard Hughes Medical Institute, Department of Neurobiology, Harvard Medical School, Boston, MA, USA.
  • Fu Z; Department of Biomedical Engineering, Boston University, Boston, MA, USA.
  • Boyden ES; Department of Biomedical Engineering, Boston University, Boston, MA, USA.
  • Han X; Media Lab, MIT, Cambridge, MA, USA.
Nature ; 574(7778): 413-417, 2019 10.
Article em En | MEDLINE | ID: mdl-31597963
ABSTRACT
A longstanding goal in neuroscience has been to image membrane voltage across a population of individual neurons in an awake, behaving mammal. Here we describe a genetically encoded fluorescent voltage indicator, SomArchon, which exhibits millisecond response times and is compatible with optogenetic control, and which increases the sensitivity, signal-to-noise ratio, and number of neurons observable several-fold over previously published fully genetically encoded reagents1-8. Under conventional one-photon microscopy, SomArchon enables the routine population analysis of around 13 neurons at once, in multiple brain regions (cortex, hippocampus, and striatum) of head-fixed, awake, behaving mice. Using SomArchon, we detected both positive and negative responses of striatal neurons during movement, as previously reported by electrophysiology but not easily detected using modern calcium imaging techniques9-11, highlighting the power of voltage imaging to reveal bidirectional modulation. We also examined how spikes relate to the subthreshold theta oscillations of individual hippocampal neurons, with SomArchon showing that the spikes of individual neurons are more phase-locked to their own subthreshold theta oscillations than to local field potential theta oscillations. Thus, SomArchon reports both spikes and subthreshold voltage dynamics in awake, behaving mice.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vigília / Biomarcadores Ambientais / Imagem Óptica / Hipocampo / Neurônios Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vigília / Biomarcadores Ambientais / Imagem Óptica / Hipocampo / Neurônios Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article