Evidence map›Paper›PMID 23750244›Full record

ArticlePloS one2013

Cell-autonomous defects in thymic epithelial cells disrupt endothelial-perivascular cell interactions in the mouse thymus.

Jerrod L Bryson, Ann V Griffith, Bernard Hughes, Fumi Saito, Yousuke Takahama, Ellen R Richie, Nancy R Manley

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  11. Pleiotropic Roles of VEGF in the Microenvironment of the Developing Thymus.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  12. Article
  13. Review
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  17. FOXN1 in thymus organogenesis and development.European journal of immunology · 2016
    Review
  18. Article
  19. Article
  20. Article
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

7 authors at 4 institutions in 2 countries.

Jerrod L BrysonDepartment of Cellular Biology, University of Georgia, Athens, Georgia, USA.
Ann V Griffith
Bernard Hughes
Fumi Saito
Yousuke Takahama
Ellen R Richie
Nancy R Manley
Tokushima University · JPGenesis Foundation · USThe University of Texas MD Anderson Cancer Center · USUniversity of Georgia · US

Funding

Regulation of thymic epithelial cell differentiationR01AI055001 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI MANLEY, NANCY R · 2003 to 2007
$1.6M
Mechanisms of cervical thymus developmentR21AI075244 · NIAID · UNIVERSITY OF GEORGIA · PI MANLEY, NANCY R · 2007 to 2008
$401k
NIAID NIH HHS AI055001NIAID NIH HHS AI075244NIAID NIH HHS R01 AI055001NIAID NIH HHS R21 AI075244
6 · The paper itself

Abstract

The thymus is composed of multiple stromal elements comprising specialized stromal microenvironments responsible for the development of self-tolerant and self-restricted T cells. Here, we investigated the ontogeny and maturation of the thymic vasculature. We show that endothelial cells initially enter the thymus at E13.5, with PDGFR-β(+) mesenchymal cells following at E14.5. Using an allelic series of the thymic epithelial cell (TEC) specific transcription factor Foxn1, we showed that these events are delayed by 1-2 days in Foxn1 (Δ/Δ) mice, and this phenotype was exacerbated with reduced Foxn1 dosage. At subsequent stages there were fewer capillaries, leaky blood vessels, disrupted endothelium - perivascular cell interactions, endothelial cell vacuolization, and an overall failure of vascular organization. The expression of both VEGF-A and PDGF-B, which are both primarily expressed in vasculature-associated mesenchyme or endothelium in the thymus, were reduced at E13.5 and E15.5 in Foxn1 (Δ/Δ) mice compared with controls. These data suggest that Foxn1 is required in TECs both to recruit endothelial cells and for endothelial cells to communicate with thymic mesenchyme, and for the differentiation of vascular-associated mesenchymal cells. These data show that Foxn1 function in TECs is required for normal thymus size and to generate the cellular and molecular environment needed for normal thymic vascularization. These data further demonstrate a novel TEC-mesenchyme-endothelial interaction required for proper fetal thymus organogenesis.

Indexed as

Cell CommunicationAllelesAnimalsBlood VesselsCell MovementCollagen Type IVEndotheliumEpithelial CellsForkhead Transcription FactorsMesodermMiceNeovascularization, PhysiologicNeural CrestRegional Blood FlowStromal CellsThymus GlandCollagen Type IVForkhead Transcription FactorsWhn protein

Identifiers

PMID23750244
PMCPMC3672159
OpenAlexW2086948379

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.