The neocortex plays a critical role in complex cognitive tasks. At a mesoscopic level, similarities in the organization of the neocortex across species suggests that cortical processing and circuit motifs are well- preserved and stereotyped. This emphasizes the relevance and boosts motivation to study non-human mammals in the hopes of understanding cortical processing in the human brain. This project aims to investigate the roles of certain cell-types in neocortical circuitry. Specifically, the goal is to comprehensively characterize the cellular components involved in a sensory-processing and learning task in the mouse primary somatosensory cortex. Neurons in the somatosensory cortex will be probed to uncover three characteristics: anatomical identity based on their projection target, functional identity based on their activity patterns during a behavioral task, and molecular identity based on their transcriptome. Anatomical identity of neurons in the somatosensory cortex will be determined by retrograde labelling from target areas. Functional identity will be characterized by in vivo two-photon calcium imaging of neuronal activity during whisker-guided decision making tasks. Molecular identity will be visualized using ex vivo fluorescence in situ hybridization targeting mRNA transcripts informative of molecular cell-type. Drawing parallels between these three characterizations will result in comprehensive definitions of cells involved, with the expectation that homologies exist in the human brain. These experiments will identify key cellular components involved in sensory-processing, decision making, and learning, which will provide critical insight into how the brain performs complex computations.

Public Health Relevance

This project will use an integrative approach consisting of novel techniques and tools to comprehensively define the cellular components involved in neocortical sensory processing, short-term memory, learning, and decision making in the mouse somatosensory cortex. Findings from this study will provide valuable insight into how cellular diversity affords the mammalian neocortex its complex cognitive abilities.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31NS111896-01
Application #
9760138
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Gnadt, James W
Project Start
2019-09-02
Project End
2022-09-01
Budget Start
2019-09-02
Budget End
2020-09-01
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Boston University
Department
Engineering (All Types)
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
049435266
City
Boston
State
MA
Country
United States
Zip Code
02215