Neural Mechanisms of Spatial Representations Beyond the Self
Project Number4R00NS126715-03
Former Number5K99NS126715-02
Contact PI/Project LeaderSTANGL, MATTHIAS
Awardee OrganizationBOSTON UNIVERSITY (CHARLES RIVER CAMPUS)
Description
Abstract Text
PROJECT SUMMARY/ABSTRACT
Spatial navigation is a fundamental human behavior, and deficits in navigational functions are among the
hallmark symptoms of severe neurological disorders such as Alzheimer’s disease. Understanding how the
human brain processes and encodes spatial information is thus of critical importance for the development of
therapies for affected patients. Previous studies have shown that the brain forms neural representations of spatial
information, via spatially-tuned activity of single neurons (e.g., place cells, grid cells, or head direction cells), and
by the coordinated oscillatory activity of cell populations. The vast majority of these studies have focused on the
encoding of self-related spatial information, such as one’s own location, orientation, and movements. However,
everyday tasks in social settings require the encoding of spatial information not only for oneself, but also for other
people in the environment. At present, it is largely unknown how the human brain accomplishes this important
function, and how aspects of human cognition may affect these spatial encoding mechanisms. This project
therefore aims to elucidate the neural mechanisms that underlie the encoding of spatial information and
awareness of others. Specifically, the proposed research plan will determine how human deep brain oscillations
and single-neuron activity allow us to keep track of other individuals as they move through our environment.
Next, the project will determine whether these spatial encoding mechanisms are specific to the encoding of
another person, or whether they can be used more flexibly to support the encoding of moving inanimate objects
and even more abstract cognitive functions such as imagined navigation. Finally, the project will determine how
spatial information is encoded in more complex real-world scenarios, when multiple information sources (e.g.,
multiple people) are present. To address these questions, intracranial medial temporal lobe activity will be
recorded from two rare participant groups: (1) Participants with permanently implanted depth electrodes for the
treatment of focal epilepsy through responsive neurostimulation (RNS), who provide a unique opportunity to
record deep brain oscillations during free movement and naturalistic behavior; and (2) hospitalized epilepsy
patients with temporarily implanted intracranial electrodes in the epilepsy monitoring unit (EMU), from whom joint
oscillatory and single-neuron activity can be recorded.
In addition, this award will allow me to complete a multifaceted career development plan: Since my current
experience with electrophysiological recordings is limited to oscillatory activity from RNS participants, I will learn
to record and analyze human single-neuron activity from EMU patients in a clinical setting. My training will be
guided by pioneers in this research area, and will take place at UCLA, one of the world’s leading institutions in
the clinical and research work with these patient populations. I will further attend seminars, coursework, and
conferences, to develop not only as an experimentalist, but also as an independent leader and science
communicator. Together, this will provide me with the necessary set of skills for my transition to independence.
Public Health Relevance Statement
PROJECT NARRATIVE
Fundamental abilities, such as keeping track of where we are, or forming episodic memories during social
experiences, critically depend on the continuous processing and encoding of spatial information about the self,
others, and the environment. Impairments in these abilities are among the hallmark symptoms of Alzheimer’s
and other neurological diseases. The proposed research therefore aims to enhance our understanding of the
neural mechanisms that underlie the encoding of spatial information and awareness of others, which will
ultimately help elucidate the neurophysiological origins of malfunctions in these systems.
National Institute of Neurological Disorders and Stroke
CFDA Code
853
DUNS Number
049435266
UEI
THL6A6JLE1S7
Project Start Date
15-May-2022
Project End Date
30-April-2027
Budget Start Date
01-June-2024
Budget End Date
30-April-2025
Project Funding Information for 2024
Total Funding
$241,421
Direct Costs
$146,316
Indirect Costs
$95,105
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Neurological Disorders and Stroke
$241,421
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 4R00NS126715-03
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 4R00NS126715-03
Patents
No Patents information available for 4R00NS126715-03
Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 4R00NS126715-03
Clinical Studies
No Clinical Studies information available for 4R00NS126715-03
News and More
Related News Releases
No news release information available for 4R00NS126715-03
History
No Historical information available for 4R00NS126715-03
Similar Projects
No Similar Projects information available for 4R00NS126715-03