Evidence map›Paper›PMID 42282817›Full record

ArticlebioRxiv : the preprint server for biology2026

Artery-Like Smooth Muscle Drives Contractile Function in Dural Venous Sinuses.

Madison E Lemire, Hannah C Ryan, Lillian S Hand, John C DeWitt, Liqun He, Christer Betsholtz, Adam S Sprouse Blum, Nicholas R Klug

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Madison E LemireDepartment of Pharmacology, Larner College of Medicine, University of Vermont, Burlington, VT 05405.ORCID 0009-0008-3505-6369
Hannah C RyanDepartment of Pharmacology, Larner College of Medicine, University of Vermont, Burlington, VT 05405.
Lillian S HandDepartment of Pharmacology, Larner College of Medicine, University of Vermont, Burlington, VT 05405.
John C DeWittDepartment of Pathology & Laboratory Medicine, Larner College of Medicine, University of Vermont, Burlington.
Liqun HeDepartment of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-2127-7597
Christer BetsholtzDepartment of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-8494-971X
Adam S Sprouse BlumDepartment of Neurological Sciences, Larner College of Medicine, University of Vermont, Burlington, VT 05405.ORCID 0000-0002-6781-707X
Nicholas R KlugDepartment of Pharmacology, Larner College of Medicine, University of Vermont, Burlington, VT 05405.ORCID 0000-0001-7540-0306

Funding

Vermont Center for Cardiovascular and Brain HealthP20GM135007 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MARY CUSHMAN, MARK T NELSON · 2020 to 2026
$17.4M
Regulation of blood flow in the brain by capillary KATP channelsK01HL167052 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Nicholas Ryan Klug · 2024 to 2026
$486k
NHLBI NIH HHS K01 HL167052NIGMS NIH HHS P20 GM135007
6 · The paper itself

Abstract

The dural venous sinuses are the main conduit for cerebral blood flow to drain from the head back to the heart. Pathology of these sinuses has significant impacts on cerebral blood volume and intracranial pressure, indicating that these veins have an important role in cerebral hemodynamics. Active and modifiable mechanisms of sinus diameter control may present an opportunity for physiological or pathological regulation of venous blood flow. Here, we characterized the molecular and anatomical properties of dural vascular smooth muscle cells (SMCs) using RNA-sequencing and immunohistochemistry, demonstrating that artery-like SMCs are exclusive to sinus vessels. An ex vivo pressurized sinus preparation from mice was used to functionally characterize the vasodynamics of the sinus and its corresponding bridging veins. We found that the sinus contains dynamically contractile SMCs and constricts to both pressure and contractile agonists, while the bridging veins do not. We further demonstrated that these sinus SMCs exhibit dynamic calcium signaling that is responsive to contractile stimuli. These results reveal a contractile SMC phenotype localized to dural venous sinuses and demonstrate that sinus vessels possess active, artery-like mechanisms for regulating cerebral venous outflow.

Identifiers

PMID42282817
PMCPMC13252089

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.