Primary visual cortex (V1) is the best studied part of the brain in multiple different mammalian species. Macaque V1 has been particularly intensively studied because of the close homologies between the visual systems of macaques and humans. We understand a great deal about the visual response properties of V1 neurons but, aside from some rough ideas about parallel pathways, we have limited understanding of how the cortical circuit transforms the visual information it receives. The rough outline of the cortical network is known, such as the axonal pathways that distribute information between the layers, but little is known of the network structure of connections between individual neurons. In particular, almost nothing is known about how visual response properties of neurons relate to their interconnections, even for pairs of neurons let alone over the entire network. Over the past decade, we have developed a new approach to studying cortical circuits?functional connectomics?that promises to address this question. Microscale connectomics has been developed by multiple groups with the goal of densely or completely mapping individual synaptic connections in the neural circuits with serial-section electron microscopy. Functional connectomics seeks to relate network structure with the physiological properties of individual neurons within a circuit. So far, virtually all research in microscale connectomics has been performed on mice or non-mammalian species. With recent advances in the scale of volumetric EM reconstructions and machine segmentation, it is time to perform cortical connectomics in species whose physiology is far better understood. In the macaque, we will use two-photon calcium imaging to record the visual responses of tens of thousands of neurons in a single circuit. This same circuit will then be reconstructed with EM connectomics, yielding a data set with rich information about visual response properties, neuronal type (as classified through morphology), and connectivity. This data set will be used to explore competing models of information in the macaque visual system. The close homology between macaque and human V1 offers a unique opportunity to compare their detailed network structure, while the structure/function relationships learned for the macaque will build a bridge for understanding the human network in a functional context.

Public Health Relevance

Many of the neurological and psychiatric diseases with the largest impact on public health?Alzheimer's disease, stroke, epilepsy, and autism?are functional disorders that likely have correlates in disordered brain connections. The proposed basic-research studies will characterize the functional connectivity of brain circuits with unprecedented resolution and completeness in both non-human primate and in the human. When applied to tissue in the context of disease, the techniques and approaches we develop will greatly improve our ability to study the relationship between altered connections and functional deficits.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY010115-24A1
Application #
9972661
Study Section
Mechanisms of Sensory, Perceptual, and Cognitive Processes Study Section (SPC)
Program Officer
Flanders, Martha C
Project Start
1993-04-01
Project End
2024-03-31
Budget Start
2020-05-01
Budget End
2021-03-31
Support Year
24
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Allen Institute
Department
Type
DUNS #
137210949
City
Seattle
State
WA
Country
United States
Zip Code
98109
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Histed, Mark H; Bonin, Vincent; Reid, R Clay (2009) Direct activation of sparse, distributed populations of cortical neurons by electrical microstimulation. Neuron 63:508-22
Ohki, Kenichi; Reid, R Clay (2007) Specificity and randomness in the visual cortex. Curr Opin Neurobiol 17:401-7

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