Evidence map›Paper›PMID 19955175›Full record

ArticleThe Journal of biological chemistry2010

Postnatal tissue-specific disruption of transcription factor FoxN1 triggers acute thymic atrophy.

Lili Cheng, Jianfei Guo, Liguang Sun, Jian Fu, Peter F Barnes, Daniel Metzger, Pierre Chambon, Robert G Oshima, Takashi Amagai, Dong-Ming Su

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

71 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Runx3 instructs AireJournal of autoimmunity · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Thymus Ontogeny and Development.Advances in experimental medicine and biology · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Generation of functional human thymic cells from induced pluripotent stem cells.The Journal of allergy and clinical immunology · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Pleiotropic Roles of VEGF in the Microenvironment of the Developing Thymus.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article

11 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 3 countries.

Lili ChengDepartment of Biomedical Research, University of Texas Health Science Center at Tyler, Tyler, Texas 75708, USA.
Jianfei Guo
Liguang Sun
Jian Fu
Peter F Barnes
Daniel Metzger
Pierre Chambon
Robert G Oshima
Takashi Amagai
Dong-Ming Su
The University of Texas Health Science Center at Tyler · USCollège de France · FRInstitute for Medical Research · USMeiji University of Integrative Medicine · JP

Funding

Molecular basis for age-related thymic involution and rejuvenationR01AI081995 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI SU, DONG-MING · 2009 to 2013
$1.9M
Strategy for Rescuing Primary Thymic Stromal FailureR21AI079747 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI SU, DONG-MING · 2008 to 2009
$388k
Molecular Regulation of Aging Thymus AtrophyR21AI064939 · NIAID · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI SU, DONG-MING · 2005 to 2006
$374k
NIAID NIH HHS R01 AI081995NIAID NIH HHS R01AI081995NIAID NIH HHS R21 AI064939NIAID NIH HHS R21AI064939NIAID NIH HHS R21 AI079747NIAID NIH HHS R21AI079747
6 · The paper itself

Abstract

The transcription factor FoxN1 is essential for differentiation of thymic epithelial cell (TEC) progenitors during thymic organogenesis. However, limited information is available on the postnatal contribution of FoxN1 to thymic maintenance. To address this question, we generated a loxP-floxed FoxN1 (fx) mouse with three different promoter-driven inducible CreER(T) transgenes. Postnatal ubiquitous deletion of FoxN1 caused dramatic thymic atrophy in 5 days and more severe deterioration in medullary TECs (mTECs) than in cortical TECs (cTECs). Induction of FoxN1 deletion selectively in K5 promoter-driven somatic epithelial cells (mostly mTECs and possibly some adult epithelial stem cells) was sufficient to cause significant thymic atrophy, whereas FoxN1 deletion in K18 promoter-driven somatic epithelial cells (mostly cTECs) was not. Thymic atrophy resulted from increased apoptosis and was associated with activation of the p53 gene in mature mTECs. Although FoxN1 is required for the development of both mTECs and cTECs in thymic organogenesis, it is most important for the maintenance of mTECs in the postnatal thymus, which are in turn necessary to prevent thymic atrophy.

Indexed as

Promoter Regions, GeneticAnimalsApoptosisAtrophyEpithelial CellsForkhead Transcription FactorsGene Knockdown TechniquesMiceMice, TransgenicStem CellsThymus GlandTime FactorsTransgenesTumor Suppressor Protein p53Forkhead Transcription FactorsTumor Suppressor Protein p53Whn protein

Identifiers

PMID19955175
PMCPMC2820809
OpenAlexW2072910535

What OpenQuestion holds

Textmetadata
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.