Evidence map›Paper›PMID 41242645›Full record

ArticleDevelopmental biology2026

PDGFRα is required for postnatal cerebral perivascular fibroblast development.

Hannah E Jones, Kelsey A Abrams, Sol Kim, Katherine A Fantauzzo, Julie A Siegenthaler

Abstract read
In one paragraph

Article in Developmental 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

5 · Who and what money

Authors and funding

5 authors.

Hannah E JonesDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA; Cell Biology, Stem Cells and Development Graduate Program, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA.
Kelsey A AbramsDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA; Cell Biology, Stem Cells and Development Graduate Program, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA.
Sol KimDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA; Cell Biology, Stem Cells and Development Graduate Program, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA.
Katherine A FantauzzoCell Biology, Stem Cells and Development Graduate Program, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA; Department of Craniofacial Biology, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA.
Julie A SiegenthalerDepartment of Pediatrics, Section of Developmental Biology, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA; Cell Biology, Stem Cells and Development Graduate Program, University of Colorado, Anschutz Medical Campus, Aurora, CO, 80045, USA. Electronic address: Julie.Siegenthaler@cuanschutz.edu.

Funding

Training Program in Perinatal Biology and MedicineT32HD007186 · NICHD · UNIVERSITY OF COLORADO DENVER · PI Paul Joseph Rozance · 1985 to 2026
$6.5M
Retinoic Acid in Development of CNS VasculatureR01NS098273 · NINDS · UNIVERSITY OF COLORADO DENVER · PI SIEGENTHALER, JULIE · 2016 to 2025
$3.2M
CNS Fibroblast Formation and FunctionR01NS131823 · NINDS · UNIVERSITY OF COLORADO DENVER · PI Julie Siegenthaler · 2024 to 2026
$1.1M
Cellular mechanisms of perivascular fibroblast development and dependence on PDGF signalingF31NS125875 · NINDS · UNIVERSITY OF COLORADO DENVER · PI JONES, HANNAH ELIZABETH · 2022 to 2024
$100k
NICHD NIH HHS T32 HD007186NINDS NIH HHS F31 NS125875NINDS NIH HHS R01 NS098273NINDS NIH HHS R01 NS131823
6 · The paper itself

Abstract

Perivascular fibroblasts (PVFs) are a cell type associated with large diameter blood vessels in the brain and spinal cord parenchyma and leptomeninges. PVFs have previously defined roles in injury and neuroinflammatory diseases and predicted roles in supporting neurovascular function. The temporal dynamics of PVF development in the pre- and postnatal cerebral cortex have recently been described, however the molecular mechanisms that underly PVF development have not been identified. PVFs express both platelet-derived growth factor receptors (PDGFRs), PDGFRα and PDGFRβ. Here we investigate the role of PDGF signaling in PVF development. We use immunohistochemistry and RNA transcript detection methods to show developmental expression of PDGFRs by PVFs and examine distribution of PDGF ligand expression in the brain. We show that postnatal deletion of PDGFRα in fibroblasts using the Col1a2-CreERT mouse line impairs PVF coverage of cerebral vessels at postnatal day 10. Perivascular macrophages, a cell type previously shown to co-develop with PVFs, have impaired cerebral vessel coverage in conditional mutants that is similar to PVF coverage defects. This work establishes a requirement for PDGFRα signaling in PVF development and may shed light upon the potential pathways that are over-activated in PVFs in injury and disease contexts.

Indexed as

Cerebral CortexFibroblastsReceptor, Platelet-Derived Growth Factor alphaAnimalsAnimals, NewbornBrainMacrophagesMicePericytesPlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor betaSignal TransductionPlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID41242645
PMCPMC13080661

What Socratic holds

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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 Socratic graph.