TY - JOUR
T1 - The Role of the Human Brain Neuron–Glia–Synapse Composition in Forming Resting-State Functional Connectivity Networks
AU - Kahali, Sayan
AU - Raichle, Marcus E.
AU - Yablonskiy, Dmitriy A.
N1 - Funding Information:
Funding: This research study was funded by NIH NIA, grant number R01 AG054513.
Funding Information:
Acknowledgments: The resting-state data of this study were provided by the Human Connec-tome Project, WU-Minn Consortium (principal investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657), funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research, and by the McDonnell Center for Systems Neuroscience at Washington University. The genetic information was obtained from the Allen Institute for Brain Science, Allen Human Brain Atlas, available from: human.brain-map.org (last accessed 10 October 2021). The authors would also like to acknowledge the helpful discussions at different stages of this project with Charles Hildebolt, Dillan Newbold, Reza Hamidian, Janine Bijsterbosch, BT Thomas Yeo, and Ryan Raut. Editing assistance was provided by InPrint: A Scientific Editing Network at Washington University in St. Louis.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12
Y1 - 2021/12
N2 - While significant progress has been achieved in studying resting-state functional networks in a healthy human brain and in a wide range of clinical conditions, many questions related to their relationship to the brain’s cellular constituents remain. Here, we use quantitative Gradient-Recalled Echo (qGRE) MRI for mapping the human brain cellular composition and BOLD (blood–oxygen level-dependent) MRI to explore how the brain cellular constituents relate to resting-state functional networks. Results show that the BOLD signal-defined synchrony of connections between cellular circuits in network-defined individual functional units is mainly associated with the regional neuronal density, while the between-functional units’ connectivity strength is also influenced by the glia and synaptic components of brain tissue cellular constituents. These mechanisms lead to a rather broad distribution of resting-state functional network properties. Visual networks with the highest neuronal density (but lowest density of glial cells and synapses) exhibit the strongest coherence of the BOLD signal as well as the strongest intra-network connectivity. The Default Mode Network (DMN) is positioned near the opposite part of the spectrum with relatively low coherence of the BOLD signal but with a remarkably balanced cellular contents, enabling DMN to have a prominent role in the overall organization of the brain and hierarchy of functional networks.
AB - While significant progress has been achieved in studying resting-state functional networks in a healthy human brain and in a wide range of clinical conditions, many questions related to their relationship to the brain’s cellular constituents remain. Here, we use quantitative Gradient-Recalled Echo (qGRE) MRI for mapping the human brain cellular composition and BOLD (blood–oxygen level-dependent) MRI to explore how the brain cellular constituents relate to resting-state functional networks. Results show that the BOLD signal-defined synchrony of connections between cellular circuits in network-defined individual functional units is mainly associated with the regional neuronal density, while the between-functional units’ connectivity strength is also influenced by the glia and synaptic components of brain tissue cellular constituents. These mechanisms lead to a rather broad distribution of resting-state functional network properties. Visual networks with the highest neuronal density (but lowest density of glial cells and synapses) exhibit the strongest coherence of the BOLD signal as well as the strongest intra-network connectivity. The Default Mode Network (DMN) is positioned near the opposite part of the spectrum with relatively low coherence of the BOLD signal but with a remarkably balanced cellular contents, enabling DMN to have a prominent role in the overall organization of the brain and hierarchy of functional networks.
KW - Brain cellular composition
KW - Default mode network
KW - Functional connectivity networks
KW - MRI
KW - QGRE
KW - Quantitative Gradient-Recalled Echo
UR - http://www.scopus.com/inward/record.url?scp=85122863453&partnerID=8YFLogxK
U2 - 10.3390/brainsci11121565
DO - 10.3390/brainsci11121565
M3 - Article
C2 - 34942867
AN - SCOPUS:85122863453
SN - 2076-3425
VL - 11
JO - Brain Sciences
JF - Brain Sciences
IS - 12
M1 - 1565
ER -