4.8 Article

The logic of single-cell projections from visual cortex

Journal

NATURE
Volume 556, Issue 7699, Pages 51-+

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nature26159

Keywords

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Funding

  1. National Institutes of Health [5RO1NS073129, 5RO1DA036913]
  2. Brain Research Foundation [BRF-SIA-2014-03]
  3. IARPA [MICrONS D16PC0008]
  4. Simons Foundation [382793/SIMONS]
  5. Paul Allen Distinguished Investigator Award
  6. Boehringer Ingelheim Fonds
  7. Genentech Foundation
  8. National Natural Science Foundation of China [NSFC 31600847]
  9. European Research Council [NeuroV1sion 616509]
  10. Swiss National Science Foundation [SNSF 31003A_169802]
  11. NATIONAL INSTITUTE OF MENTAL HEALTH [RF1MH114132] Funding Source: NIH RePORTER
  12. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS073129] Funding Source: NIH RePORTER
  13. NATIONAL INSTITUTE ON DRUG ABUSE [R01DA036913] Funding Source: NIH RePORTER

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Neocortical areas communicate through extensive axonal projections, but the logic of information transfer remains poorly understood, because the projections of individual neurons have not been systematically characterized. It is not known whether individual neurons send projections only to single cortical areas or distribute signals across multiple targets. Here we determine the projection patterns of 591 individual neurons in the mouse primary visual cortex using whole-brain fluorescence-based axonal tracing and high-throughput DNA sequencing of genetically barcoded neurons (MAPseq). Projections were highly diverse and divergent, collectively targeting at least 18 cortical and subcortical areas. Most neurons targeted multiple cortical areas, often in non-random combinations, suggesting that sub-classes of intracortical projection neurons exist. Our results indicate that the dominant mode of intracortical information transfer is not based on 'one neuron-one target area' mapping. Instead, signals carried by individual cortical neurons are shared across subsets of target areas, and thus concurrently contribute to multiple functional pathways.

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