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Award Abstract # 1942360
CAREER: Astrocytic Integration of Cortical Wake Signals

NSF Org: IOS
Division Of Integrative Organismal Systems
Recipient: REGENTS OF THE UNIVERSITY OF CALIFORNIA, SAN FRANCISCO, THE
Initial Amendment Date: April 20, 2020
Latest Amendment Date: November 30, 2022
Award Number: 1942360
Award Instrument: Continuing Grant
Program Manager: Edda Thiels
ethiels@nsf.gov
 (703)292-8167
IOS
 Division Of Integrative Organismal Systems
BIO
 Directorate for Biological Sciences
Start Date: May 1, 2020
End Date: October 31, 2022 (Estimated)
Total Intended Award Amount: $740,000.00
Total Awarded Amount to Date: $278,000.00
Funds Obligated to Date: FY 2020 = $278,000.00
FY 2021 = $0.00

FY 2022 = $0.00
History of Investigator:
  • Kira Poskanzer (Principal Investigator)
    Kira.Poskanzer@ucsf.edu
Recipient Sponsored Research Office: University of California-San Francisco
1855 FOLSOM ST STE 425
SAN FRANCISCO
CA  US  94103-4249
(415)476-2977
Sponsor Congressional District: 11
Primary Place of Performance: University of California-San Francisco
1550 4th Street
San Francisco
CA  US  94143-2200
Primary Place of Performance
Congressional District:
11
Unique Entity Identifier (UEI): KMH5K9V7S518
Parent UEI: KMH5K9V7S518
NSF Program(s): Modulation
Primary Program Source: 01002021DB NSF RESEARCH & RELATED ACTIVIT
01002122DB NSF RESEARCH & RELATED ACTIVIT

01002223DB NSF RESEARCH & RELATED ACTIVIT

01002324DB NSF RESEARCH & RELATED ACTIVIT

01002425DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 1045, 1096, 9178, 9179
Program Element Code(s): 771400
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.074

ABSTRACT

The fundamental biological importance of sleep is demonstrated by the fact that sleep is observed widely across the animal kingdom, and that sleep deprivation can be harmful both physiologically and cognitively. Likewise, the importance of wake is axiomatic: reproduction, feeding, and escape from predation depend on an animal being awake. However, until recently, the neural circuits that regulate wake and sleep have remained poorly understood. One strand of inquiry has implicated a non-neuronal cell type in sleep-wake control. This cell?the astrocyte?makes up the largest class of non-neuronal cells in the brain, and it has been shown to affect the activity of surrounding neurons. However, the ways in which astrocytes are involved in sleep and wake are largely unexplored. This project tests whether astrocytes sense wake-specific signals and respond to these signals by changing the state of the brain. To perform these experiments, advanced imaging tools to watch different forms of cellular activity in the brain are used. The broader impacts of this project aim to make interdisciplinary research accessible and routine to trainees early in their careers. The motivation for this lies in the fact that trainees with experience in physical sciences are more likely to become tool builders themselves, and that watching science happening in real time can excite and empower trainees to think deeply about the biology around them.

Neuromodulatory signaling is critical for animal behavior, in part by shifting the brain among various states, and the most dramatic brain state shifts are arguably those that occur between wake and sleep. However, how neuromodulatory inputs arising in subcortical nuclei are integrated at the level of the cortex to regulate population-level state shifts remains unclear. Several neuromodulatory receptors are expressed on both cortical neurons and astrocytes, raising the possibility that astrocytes are partners with neurons in sensing neuromodulatory cues to initiate and/or maintain wake in the cortex. Astrocytes are an attractive target for coordinating large-scale neuronal circuit changes, and they have also been implicated in sleep/wake via brain state-dependent changes in extracellular balance and morphology. The overarching hypothesis for this project is that neuromodulatory signaling to astrocytes, and subsequent astrocytic effects on population neuronal activity, is critical for integrating wake-state signals in the cortex, the largest area of the mammalian brain. The research addresses these questions using advanced two-photon imaging, modern neurobiological tools to modulate neural activity, and astrocyte-specific technology to probe the cell biological responses of astrocytes to neuromodulatory cues, and map astrocytic dynamics across wake and sleep, in preparation to test the effects of astrocyte activation on wake state and neural signaling in a cortical circuit.

This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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Pittolo, Silvia and Yokoyama, Sae and Willoughby, Drew D. and Taylor, Charlotte R. and Reitman, Michael E. and Tse, Vincent and Wu, Zhaofa and Etchenique, Roberto and Li, Yulong and Poskanzer, Kira E. "Dopamine activates astrocytes in prefrontal cortex via 1-adrenergic receptors" Cell Reports , v.40 , 2022 https://doi.org/10.1016/j.celrep.2022.111426 Citation Details
Vaidyanathan, Trisha V and Collard, Max and Yokoyama, Sae and Reitman, Michael E and Poskanzer, Kira E "Cortical astrocytes independently regulate sleep depth and duration via separate GPCR pathways" eLife , v.10 , 2021 https://doi.org/10.7554/eLife.63329 Citation Details

PROJECT OUTCOMES REPORT

Disclaimer

This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.

The goal of this project was to determine the mechanisms by which neuromodulatory control by astrocytes affects sleep and wake states in the mammalian cerebral cortex. In this project, the Poskanzer lab and collaborators showed that manipulation of astrocytes in the mouse cortex could change both sleep depth and sleep duration, depending on the specific type of G-protein-coupled receptors (GPCRs) which were stimulated. These results showed not only that astrocytes can regulate neuronal networks underlying sleep and wake, but also that these two sleep features are mechanistically separable. Following up on these findings, the lab has worked to show that specific neuromodulators and receptors are responsible for sensing wake- and sleep-specific signals in the cortex from subcortical structures. Dopamine, histamine, and norepinephrine and their receptors have all been loci for inquiry.

 

Focusing on the wake state, the Poskanzer lab—with collaborators in image analysis, mouse genetics, and transcriptomics—found that cortical astrocytes in the primary visual cortex are critical for sensing both small and large changes in norepinephrine, and resynchronizing cortical circuits after increases in arousal/attention. Genetic deletion of a specific adrenergic receptor on astrocytes confirmed that astrocytes work alongside neurons to regulate cortical state. These results open up the possibility for understanding a fundamental integrative signaling code for neuromodulators in astrocytes, as computational partners with neurons in neurobiological circuits.

 


Last Modified: 01/10/2023
Modified by: Kira Poskanzer

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