Evidence map›Paper›PMID 35559672›Full record

ArticleScience advances2022

Developmental dynamics of the neural crest-mesenchymal axis in creating the thymic microenvironment.

Adam E Handel, Stanley Cheuk, Fatima Dhalla, Stefano Maio, Tania Hübscher, Ioanna Rota, Mary E Deadman, Olov Ekwall, Matthias Lütolf, Kenneth Weinberg and 1 more

Abstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Mesenchymal cells rebuild the thymus.Nature biotechnology · 2026
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  16. Assembling the thymus medulla: Development and function of epithelial cell heterogeneity.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
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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

11 authors.

Adam E HandelDepartment of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID 0000-0001-8385-6346
Stanley CheukDepartment of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID 0000-0002-2759-3884
Fatima DhallaDepartment of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID 0000-0001-9244-2284
Stefano MaioDepartment of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID 0000-0001-9518-6466
Tania HübscherLaboratory of Stem Cell Bioengineering, Swiss Federal Institute of Technology in Lausanne, Lausanne, Switzerland.ORCID 0000-0002-2376-712X
Ioanna RotaDepartment of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID 0000-0002-2093-2986
Mary E DeadmanDepartment of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID 0000-0002-6074-017X
Olov EkwallDepartment of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden.ORCID 0000-0002-4506-9955
Matthias LütolfLaboratory of Stem Cell Bioengineering, Swiss Federal Institute of Technology in Lausanne, Lausanne, Switzerland.ORCID 0000-0002-5898-305X
Kenneth WeinbergDivision of Stem Cell Transplantation and Regenerative Medicine Department of Pediatrics, Stanford University, Stanford, CA, USA.ORCID 0000-0003-1922-9131
Georg HolländerDepartment of Paediatrics and the Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.ORCID 0000-0002-8790-0874

Funding

Medical Research Council MR/S036334/1Medical Research Council MR/S036407/1
6 · The paper itself

Abstract

The thymic stroma is composed of epithelial and nonepithelial cells providing separate microenvironments controlling homing, differentiation, and selection of hematopoietic precursor cells to functional T cells. Here, we explore at single-cell resolution the complex composition and dynamic changes of the nonepithelial stromal compartment across different developmental stages in the human and mouse thymus, and in an experimental model of the DiGeorge syndrome, the most common form of human thymic hypoplasia. The detected gene expression signatures identify previously unknown stromal subtypes and relate their individual molecular profiles to separate differentiation trajectories and functions, revealing an unprecedented heterogeneity of different cell types that emerge at discrete developmental stages and vary in their expression of key regulatory signaling circuits and extracellular matrix components. Together, these findings highlight the dynamic complexity of the nonepithelial thymus stroma and link this to separate instructive roles essential for normal thymus organogenesis and tissue maintenance.

Identifiers

PMID35559672
PMCPMC9106291

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Registered trials

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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.