Evidence map›Paper›PMID 38112237›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2024

Identification of distinct vascular mural cell populations during zebrafish embryonic development.

Sarah Colijn, Miku Nambara, Gracie Malin, Elena A Sacchetti, Amber N Stratman

Open access · greenAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sarah ColijnDepartment of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.
Miku NambaraDepartment of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.
Gracie MalinDepartment of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.
Elena A SacchettiDepartment of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.
Amber N StratmanDepartment of Cell Biology and Physiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri, USA.ORCID 0000-0002-8111-4186
Washington University in St. Louis · US

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Mechanosensitive mechanisms regulating cellular coordination during tissue morphogenesis and patterningR35GM137976 · NIGMS · WASHINGTON UNIVERSITY · PI STRATMAN, AMBER NICOLE · 2020 to 2024
$2.4M
NCATS NIH HHS UL1 TR002345NCATS NIH HHS UL1TR002345NIGMS NIH HHS R35 GM137976
6 · The paper itself

Abstract

backgroundMural cells are an essential perivascular cell population that associate with blood vessels and contribute to vascular stabilization and tone. In the embryonic zebrafish vasculature, pdgfrb and tagln are commonly used as markers for identifying pericytes and vascular smooth muscle cells. However, the overlapping and distinct expression patterns of these markers in tandem have not been fully described.

resultsHere, we used the Tg(pdgfrb:Gal4FF; UAS:RFP) and Tg(tagln:NLS-EGFP) transgenic lines to identify single- and double-positive perivascular cell populations on the cranial, axial, and intersegmental vessels between 1 and 5 days postfertilization. From this comparative analysis, we discovered two novel regions of tagln-positive cell populations that have the potential to function as mural cell precursors. Specifically, we found that the hypochord-a reportedly transient structure-contributes to tagln-positive cells along the dorsal aorta. We also identified a unique mural cell progenitor population that resides along the midline between the neural tube and notochord and contributes to intersegmental vessel mural cell coverage.

conclusionTogether, our findings highlight the variability and versatility of tracking both pdgfrb and tagln expression in mural cells of the developing zebrafish embryo and reveal unexpected embryonic cell populations that express pdgfrb and tagln.

Indexed as

Animals, Genetically ModifiedPericytesZebrafishZebrafish ProteinsAnimalsBlood VesselsEmbryonic DevelopmentEmbryo, NonmammalianReceptor, Platelet-Derived Growth Factor betaReceptor, Platelet-Derived Growth Factor betaZebrafish Proteinshypochordmural cell progenitorpericyteperivascular cellssclerotomevSMCzebrafish

Identifiers

PMID38112237
PMCPMC11065631
OpenAlexW4389950456

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.