We propose to design and build a device that will push the boundaries of existing technology for imaging the activity of large-scale neuronal networks at high speed and single cell resolution. This will be done by using a Multiplexed Scanned Temporal Focusing (MuST) strategy in combination with laser systems with optimized pulse characteristics. Our approach will enable unbiased calcium imaging of unprecedentedly large V-FOVs (500x500x500um at 20Hz, or 1x1x0.7mm at 3Hz) at multi-hertz time resolution. Such an imaging system has the potential to revolutionize neuroscience, providing, for the first time, the ability to monitor the dynamics of network activity of tens of thousands of neurons near-simultaneously. In the mammalian cortex this capability provides the opportunity to gain insights into the computational principles for information processing as it will allow capturing an correlating the dynamics of the network activity across cortical layers. Our technology will be developed through an iterative and in a user-led fashion with our collaborator at Columbia University where it will be made accessible to the neuroscience community. The dissemination of this technique will be further facilitated by providing a dedicated website including open source code and detailed list of materials and instructions for its design and operation.

Public Health Relevance

Understanding how neural networks perform cognitively relevant functions is a major goal of modern neuroscience, which requires the ability to record simultaneously, and independently from large of neurons that make up even the simplest networks. This task has been hampered by the lack of available tools and technologies. Our proposed design for a new type of optical microscope addresses this problem by enabling the near simultaneous recording of activity from tens of thousands of neurons in the rodent brain, thereby providing a major leap in promoting our understand of fundamental principles of information processing in the mammalian brain during health and pathological states of the human brain.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01NS094263-01
Application #
9011561
Study Section
Special Emphasis Panel (ZNS1)
Program Officer
Talley, Edmund M
Project Start
2015-09-30
Project End
2018-07-31
Budget Start
2015-09-30
Budget End
2016-07-31
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Rockefeller University
Department
Microbiology/Immun/Virology
Type
Graduate Schools
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Weisenburger, Siegfried; Vaziri, Alipasha (2018) A Guide to Emerging Technologies for Large-Scale and Whole-Brain Optical Imaging of Neuronal Activity. Annu Rev Neurosci 41:431-452
Prevedel, Robert; Verhoef, Aart J; PernĂ­a-Andrade, Alejandro J et al. (2016) Fast volumetric calcium imaging across multiple cortical layers using sculpted light. Nat Methods 13:1021-1028