4.3 Article

Three-dimensional mapping of microcircuit correlation structure

Journal

FRONTIERS IN NEURAL CIRCUITS
Volume 7, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fncir.2013.00151

Keywords

acousto-optical deflectors; two-photon imaging; motion-tracking; correlation structure; microcircuit activity; population coding

Categories

Funding

  1. National Eye Institute-United States National Institutes of Health (NIH, NEI, NIDA, NIMH) [5R01DA028525, 5-T32-EY07001-37, 5-P30-EY002520-33]
  2. National Eye Institute-United States National Institutes of Health (NIH-Pioneer award) [DPI EY023176]
  3. McKnight Scholar Award
  4. Arnold and Beckman Foundation Young Investigator Award
  5. NIMH [F30 MH088228-04]

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Great progress has been made toward under standing the properties of single neurons, yet the principles underlying interactions between neurons remain poorly understood. Given that connectivity in the neocortex is locally dense through both horizontal and vertical connections, it is of particular importance to characterize the activity structure of local populations of neurons arranged in three dimensions. However, techniques for simultaneously measuring microcircuit activity are lacking. We developed an in vivo 3D high-speed, random-access two-photon microscope that is capable of simultaneous 3D motion tracking. This allows imaging from hundreds of neurons at several hundred Hz, while monitoring tissue movement. Given that motion will induce common artifacts across the population, accurate motion tracking is absolutely necessary for studying population activity with random-access based imaging methods. We demonstrate the potential of this imaging technique by measuring the correlation structure of large populations of nearby neurons in the mouse visual cortex, and find that the micro circuit correlation structure is stimulus dependent. Three-dimensional random access multiphoton imaging with con current motion tracking provides a novel, powerful method to characterize the microcircuit activity in vivo.

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