Evidence map›Paper›PMID 37917195›Full record

ArticleThe Journal of clinical investigation2023

Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice.

Matt J Matrongolo, Phillip S Ang, Junbing Wu, Aditya Jain, Joshua K Thackray, Akash Reddy, Chi Chang Sung, Gaëtan Barbet, Young-Kwon Hong, Max A Tischfield

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% of its field
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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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  10. Reconstructing cerebral lymphatic clearance: an emerging target in the Alzheimer's disease therapeutic pipeline.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Matt J MatrongoloDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, New Jersey, USA.
Phillip S AngDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, New Jersey, USA.
Junbing WuDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, New Jersey, USA.
Aditya JainDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, New Jersey, USA.
Joshua K ThackrayChild Health Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Akash ReddyDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, New Jersey, USA.
Chi Chang SungChild Health Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Gaëtan BarbetChild Health Institute of New Jersey, Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
Young-Kwon HongDepartment of Surgery, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Max A TischfieldDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, New Jersey, USA.
Rutgers, The State University of New Jersey · USJohnson University · USUniversity of Southern California · US

Funding

The effects of skull malformations and intracranial hypertension on the glymphatic and meningeal lymphatic systems in craniosynostosisR03DE032409 · NIDCR · RUTGERS, THE STATE UNIV OF N.J. · PI TISCHFIELD, MAX · 2023 to 2023
$302k
NIDCR NIH HHS R03 DE032409
6 · The paper itself

Abstract

Skull development coincides with the onset of cerebrospinal fluid (CSF) circulation, brain-CSF perfusion, and meningeal lymphangiogenesis, processes essential for brain waste clearance. How these processes are affected by craniofacial disorders such as craniosynostosis are poorly understood. We report that raised intracranial pressure and diminished CSF flow in craniosynostosis mouse models associate with pathological changes to meningeal lymphatic vessels that affect their sprouting, expansion, and long-term maintenance. We also show that craniosynostosis affects CSF circulatory pathways and perfusion into the brain. Further, craniosynostosis exacerbates amyloid pathology and plaque buildup in Twist1+/-:5xFAD transgenic Alzheimer's disease models. Treating craniosynostosis mice with Yoda1, a small molecule agonist for Piezo1, reduces intracranial pressure and improves CSF flow, in addition to restoring meningeal lymphangiogenesis, drainage to the deep cervical lymph nodes, and brain-CSF perfusion. Leveraging these findings, we show that Yoda1 treatments in aged mice with reduced CSF flow and turnover improve lymphatic networks, drainage, and brain-CSF perfusion. Our results suggest that CSF provides mechanical force to facilitate meningeal lymphatic growth and maintenance. Additionally, applying Yoda1 agonist in conditions with raised intracranial pressure and/or diminished CSF flow, as seen in craniosynostosis or with ageing, is a possible therapeutic option to help restore meningeal lymphatic networks and brain-CSF perfusion.

Indexed as

CraniosynostosesGlymphatic SystemLymphatic VesselsAnimalsBrainDrainageIon ChannelsMicePerfusionIon ChannelsPiezo1 protein, mouseGenetic diseasesMouse modelsNeuroscienceVascular Biology

Identifiers

PMID37917195
PMCPMC10866656
OpenAlexW4388233978

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.