Evidence map›Paper›PMID 37756588›Full record

ArticleDevelopment (Cambridge, England)2023

Meningeal origins and dynamics of perivascular fibroblast development on the mouse cerebral vasculature.

Hannah E Jones, Vanessa Coelho-Santos, Stephanie K Bonney, Kelsey A Abrams, Andy Y Shih, Julie A Siegenthaler

Open access · bronzeAbstract read
In one paragraph

Article in Development (Cambridge, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

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  13. Imatinib on target in stroke recovery.The Journal of clinical investigation · 2025
    Article
  14. Development of perivascular astrocyte processes.Frontiers in neuroscience · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Hannah E JonesDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, Aurora, CO 80045, USA.
Vanessa Coelho-SantosCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Stephanie K BonneyCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Kelsey A AbramsDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, Aurora, CO 80045, USA.
Andy Y ShihCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA 98101, USA.
Julie A SiegenthalerDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, Aurora, CO 80045, USA.ORCID 0000-0003-3700-6441
Seattle Children's Hospital · USUniversity of Colorado Denver · US

Funding

Retinoic Acid in Development of CNS VasculatureR01NS098273 · NINDS · UNIVERSITY OF COLORADO DENVER · PI SIEGENTHALER, JULIE · 2016 to 2025
$3.2M
Predoctoral Training in the Genetics of Development, Disease and RegenerationT32GM141742 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI Bruce H Appel, Jeffrey Kyle Moore · 2021 to 2026
$1.9M
Exploring brain perivascular fibroblasts in health and cerebral amyloid angiopathyK99AG080034 · NIA · SEATTLE CHILDREN'S HOSPITAL · PI BONNEY, STEPHANIE · 2023 to 2024
$263k
Cellular Behaviors of Perivascular Fibroblasts in Cerebral IschemiaF32NS117649 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI BONNEY, STEPHANIE · 2020 to 2021
$131k
Cellular mechanisms of perivascular fibroblast development and dependence on PDGF signalingF31NS125875 · NINDS · UNIVERSITY OF COLORADO DENVER · PI JONES, HANNAH ELIZABETH · 2022 to 2024
$100k
NIA NIH HHS K99 AG080034NIGMS NIH HHS 1T32GM141742-01NIGMS NIH HHS T32 GM141742NINDS NIH HHS F31 NS125875NINDS NIH HHS F31NS125875-01NINDS NIH HHS F32 NS117649NINDS NIH HHS NS125875NINDS NIH HHS R01 NS098273
6 · The paper itself

Abstract

Perivascular fibroblasts (PVFs) are a fibroblast-like cell type that reside on large-diameter blood vessels in the adult meninges and central nervous system (CNS). PVFs contribute to fibrosis following injury but their homeostatic functions are not defined. PVFs were previously shown to be absent from most brain regions at birth and are only detected postnatally within the cerebral cortex. However, the origin, timing and cellular mechanisms of PVF development are not known. We used Col1a1-GFP and Col1a2-CreERT2 transgenic mice to track PVF development postnatally. Using lineage tracing and in vivo imaging we show that brain PVFs originate from the meninges and are first seen on parenchymal cerebrovasculature at postnatal day (P) 5. After P5, PVF coverage of the cerebrovasculature expands via local cell proliferation and migration from the meninges. Finally, we show that PVFs and perivascular macrophages develop concurrently. These findings provide the first complete timeline for PVF development in the brain, enabling future work into how PVF development is coordinated with cell types and structures in and around the perivascular spaces to support normal CNS vascular function.

Indexed as

FibroblastsMeningesMice, TransgenicAnimalsBrainCell MovementCell ProliferationCerebral CortexMacrophagesMiceCell migrationCerebral vasculatureMeningesMiceNeurovascular unitPerivascular macrophagesPerivascular spaces

Identifiers

PMID37756588
PMCPMC10565218
OpenAlexW4387088563

What OpenQuestion holds

Textmetadata
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.