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Brain-wide circuit interrogation at the cellular level guided by online analysis of neuronal function.
Vladimirov, Nikita; Wang, Chen; Höckendorf, Burkhard; Pujala, Avinash; Tanimoto, Masashi; Mu, Yu; Yang, Chao-Tsung; Wittenbach, Jason D; Freeman, Jeremy; Preibisch, Stephan; Koyama, Minoru; Keller, Philipp J; Ahrens, Misha B.
Affiliation
  • Vladimirov N; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA. nikita.vladimirov@gmail.com.
  • Wang C; Berlin Institute for Medical Systems Biology (BIMSB), Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany. nikita.vladimirov@gmail.com.
  • Höckendorf B; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Pujala A; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Tanimoto M; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Mu Y; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Yang CT; Nagoya University, Nagoya, Japan.
  • Wittenbach JD; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Freeman J; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Preibisch S; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Koyama M; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.
  • Keller PJ; Chan Zuckerberg Initiative, San Francisco, CA, USA.
  • Ahrens MB; Berlin Institute for Medical Systems Biology (BIMSB), Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Nat Methods ; 15(12): 1117-1125, 2018 12.
Article in En | MEDLINE | ID: mdl-30504888
ABSTRACT
Whole-brain imaging allows for comprehensive functional mapping of distributed neural pathways, but neuronal perturbation experiments are usually limited to targeting predefined regions or genetically identifiable cell types. To complement whole-brain measures of activity with brain-wide manipulations for testing causal interactions, we introduce a system that uses measured activity patterns to guide optical perturbations of any subset of neurons in the same fictively behaving larval zebrafish. First, a light-sheet microscope collects whole-brain data that are rapidly analyzed by a distributed computing system to generate functional brain maps. On the basis of these maps, the experimenter can then optically ablate neurons and image activity changes across the brain. We applied this method to characterize contributions of behaviorally tuned populations to the optomotor response. We extended the system to optogenetically stimulate arbitrary subsets of neurons during whole-brain imaging. These open-source methods enable delineating the contributions of neurons to brain-wide circuit dynamics and behavior in individual animals.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Behavior, Animal / Zebrafish / Brain / Brain Mapping / Online Systems / Larva / Neurons Limits: Animals Language: En Journal: Nat Methods Year: 2018 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Behavior, Animal / Zebrafish / Brain / Brain Mapping / Online Systems / Larva / Neurons Limits: Animals Language: En Journal: Nat Methods Year: 2018 Document type: Article