Brain endothelial gap junction coupling enables rapid vasodilation propagation during neurovascular coupling

To meet the brain's moment-to-moment energy demand, neural activation rapidly increases local blood flow. This process, known as neurovascular coupling, involves rapid, coordinated vasodilation of the brain's arterial network. Here, we demonstrate that endothelial gap junction coupling enables long-range propagation of vasodilation signals through the vasculature during neurovascular coupling. The molecular composition of these gap junctions is zonated along the arterio-venous axis, with arteries being the most strongly coupled segment. Using optogenetics and visual stimuli in awake mice, we found that acute, arterial endothelial cell type-specific deletion of Cx37 and Cx40 abolishes arterial gap junction coupling and results in impaired vasodilation. Specifically, we demonstrated that arterial endothelial gap junction coupling determines both the speed and the spatial extent of vasodilation propagation elicited by neural activity. These findings indicate that endothelial gap junctions serve as a signaling highway for neurovascular coupling, enabling flexible and efficient distribution of limited energetic resources.

Authors

Institutions

Publication Details

Journal
Cell
Published
2025-07-16
DOI
https://doi.org/10.1016/j.cell.2025.06.030
Citations
13
Primary Topic
Connexins and lens biology
Type
article
Field-Weighted Citation Impact
10.48

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Brain endothelial gap junction coupling enables rapid vasodilation propagation during neurovascular coupling

Trevor Krolak, Austin Birmingham, Benjamin E. Deverman, Kathleen Navas et al.
13 citations
Cell
Connexins and lens biology
10.48
article

Brain endothelial gap junction coupling enables rapid vasodilation propagation during neurovascular coupling

Trevor Krolak, Austin Birmingham, Benjamin E. Deverman, Kathleen Navas, Luke Kaplan, Zhuhao Wu, Megan Powell, Daniel Ryvkin, Lujing Chen, Victoria Izsa, Chenghua Gu
article en
13 citations

Abstract

To meet the brain's moment-to-moment energy demand, neural activation rapidly increases local blood flow. This process, known as neurovascular coupling, involves rapid, coordinated vasodilation of the brain's arterial network. Here, we demonstrate that endothelial gap junction coupling enables long-range propagation of vasodilation signals through the vasculature during neurovascular coupling. The molecular composition of these gap junctions is zonated along the arterio-venous axis, with arteries being the most strongly coupled segment. Using optogenetics and visual stimuli in awake mice, we found that acute, arterial endothelial cell type-specific deletion of Cx37 and Cx40 abolishes arterial gap junction coupling and results in impaired vasodilation. Specifically, we demonstrated that arterial endothelial gap junction coupling determines both the speed and the spatial extent of vasodilation propagation elicited by neural activity. These findings indicate that endothelial gap junctions serve as a signaling highway for neurovascular coupling, enabling flexible and efficient distribution of limited energetic resources.

CellVol. 188(18)
Broad Institute (US), Howard Hughes Medical Institute (US), Harvard University (US), Cornell University (US), MIND Research Institute (US)
Fidelity Biosciences, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke
Zero hunger
Openalex Percentile: Top 1%
Connexins and lens biology
10.48
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.