Evidence map›Paper›PMID 25148026›Full record

ArticleImmunity2014

Adult thymus contains FoxN1(-) epithelial stem cells that are bipotent for medullary and cortical thymic epithelial lineages.

Ahmet Ucar, Olga Ucar, Paula Klug, Sonja Matt, Fabian Brunk, Thomas G Hofmann, Bruno Kyewski

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.6field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 94 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Ahmet UcarDivision of Developmental Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany; Cellular Senescence Group, German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance, 69120 Heidelberg, Germany.
Olga UcarDivision of Developmental Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Paula KlugDivision of Developmental Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Sonja MattCellular Senescence Group, German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance, 69120 Heidelberg, Germany.
Fabian BrunkDivision of Developmental Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Thomas G HofmannCellular Senescence Group, German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance, 69120 Heidelberg, Germany. Electronic address: t.hofmann@dkfz.de.
Bruno KyewskiDivision of Developmental Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. Electronic address: b.kyewski@dkfz.de.
German Cancer Research Center · DEDKFZ-ZMBH Alliance · DEHeidelberg University · DE

Funding

European Research Council 294477
6 · The paper itself

Abstract

Within the thymus, two major thymic epithelial cell (TEC) subsets-cortical and medullary TECs-provide unique structural and functional niches for T cell development and establishment of central tolerance. Both lineages are believed to originate from a common progenitor cell, yet the cellular and molecular identity of these bipotent TEC progenitors/stem cells remains ill defined. Here we identify rare stromal cells in the murine adult thymus, which under low-attachment conditions formed spheres (termed "thymospheres"). These thymosphere-forming cells (TSFCs) displayed the stemness features of being slow cycling, self-renewing, and bipotent. TSFCs could be significantly enriched based on their distinct surface antigen phenotype. The FoxN1 transcription factor was dispensable for TSFCs maintenance in situ and for commitment to the medullary and cortical TEC lineages. In summary, this study presents the characterization of the adult thymic epithelial stem cells and demonstrates the dispensability of FoxN1 function for their stemness.

Indexed as

AnimalsAntigens, LyAntigens, NeoplasmCD24 AntigenCell Adhesion MoleculesCell DifferentiationCell LineageCells, CulturedChild, PreschoolEpithelial Cell Adhesion MoleculeEpithelial CellsFemaleForkhead Transcription FactorsHumansInfantLeukocyte Common AntigensAntigens, LyAntigens, NeoplasmCD24 AntigenCd24a protein, mouseCell Adhesion MoleculesEpithelial Cell Adhesion MoleculeForkhead Transcription FactorsLeukocyte Common AntigensLy6a protein, mouseMembrane ProteinsPtprc protein, mouseWhn protein

Identifiers

PMID25148026
PMCPMC4148705
OpenAlexW2045683334

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.