Imaging of Functional Connectivity in the Mouse Brain
Open accessAbstract
Functional neuroimaging (e.g., with fMRI) has been difficult to perform in mice, making it challenging to translate between human fMRI studies and molecular and genetic mechanisms. A method to easily perform large-scale functional neuroimaging in mice would enable the discovery of functional correlates of genetic manipulations and bridge with mouse models of disease. To satisfy this need, we combined resting-state functional connectivity mapping with optical intrinsic signal imaging (fcOIS). We demonstrate functional connectivity in mice through highly detailed fcOIS mapping of resting-state networks across most of the cerebral cortex. Synthesis of multiple network connectivity patterns through iterative parcellation and clustering provides a comprehensive map of the functional neuroarchitecture and demonstrates identification of the major functional regions of the mouse cerebral cortex. The method relies on simple and relatively inexpensive camera-based equipment, does not require exogenous contrast agents and involves only reflection of the scalp (the skull remains intact) making it minimally invasive. In principle, fcOIS allows new paradigms linking human neuroscience with the power of molecular/genetic manipulations in mouse models.
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fcOIS is a sensitive imaging modality capable of measuring functional connectivity between brain regions in healthy mice.
“We have shown previously that fcOIS is a sensitive imaging modality capable of measuring functional connectivity between brain regions in healthy mice (White et al., 2011;Bero et al., 2012)”
From Anti-ApoE Antibody Given after Plaque Onset Decreases Aβ Accumulation and Improves Brain Function in a Mouse Model of Aβ Amyloidosis (2014) · cites this paper as White et al., 2011
Bilateral functional connectivity in the HJ6.3 group appeared more globally restored and resembled that of healthy wild-type mice.
“Compared with PBS-treated mice, bilateral functional connectivity in the HJ6.3 group appeared to be more globally restored and to resemble that of healthy, wild-type mice (Fig. 7C), as described previously (White et al., 2011;Bero et al., 2012).”
From Anti-ApoE Antibody Given after Plaque Onset Decreases Aβ Accumulation and Improves Brain Function in a Mouse Model of Aβ Amyloidosis (2014) · cites this paper as White et al., 2011
There is functional disruption in APP/PS1 mice after Aβ deposition.
“and that there is functional disruption in APP/PS1 mice after A deposition (White et al., 2011;Bero et al., 2012).”
From Anti-ApoE Antibody Given after Plaque Onset Decreases Aβ Accumulation and Improves Brain Function in a Mouse Model of Aβ Amyloidosis (2014) · cites this paper as White et al., 2011
The Methods and Results describe functional-connectivity imaging in Swiss Webster mice, not APP/PS1 mice. The Discussion proposes imaging Alzheimer’s disease models as a future application; our copy does not report functional disruption after Aβ deposition (searched for APP/PS1, amyloid deposition, and related terms). (LLM, conf=0.76)
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- Authors
- White, B. R., Bauer, A. Q., Snyder, A. Z., Schlaggar, B. L., Lee, J.-M., & Culver, J. P.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Culver, Joseph P.
- ORCID
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2011-01-20
- Volume
- 6
- Issue
- 1
- Pages
- e16322
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC3024435
- OpenAlex
- W2065496603
- Cited by
- 253
- References
- 60
- Citations by year
- 2026: 7 · 2025: 15 · 2024: 18 · 2023: 25 · 2022: 16 · 2021: 15 · 2020: 15 · 2019: 22 · 2018: 15 · 2017: 30 · 2016: 16 · 2015: 9 · 2014: 23 · 2013: 16 · 2012: 7
- FWCI
- 7.96
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- National Institutes of Health
- National Institute on Drug Abuse (T90DA022871)
- National Institute of Neurological Disorders and Stroke (P01 NS32636, R01NS084028, P01NS032636)
- National Institute of Biomedical Imaging and Bioengineering (R01EB008085, R01EB009233)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Optical Imaging and Spectroscopy Techniques
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced MRI Techniques and Applications
- Keywords
- functional connectivity, mouse brain, resting-state networks, intrinsic signal imaging, mouse models of human disease, non-invasive brain imaging, camera-based imaging
- MeSH terms
- Animals, Brain Mapping, Cerebral Cortex, Equipment Design, Magnetic Resonance Imaging, Methods, Neural Pathways, Mice, Optical Devices
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