Evidence map›Paper›PMID 18832676›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Alterations of the medullary epithelial compartment in the Aire-deficient thymus: implications for programs of thymic epithelial differentiation.

James Dooley, Matthew Erickson, Andrew G Farr

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Aire in Autoimmunity.Annual review of immunology · 2024
    Review
  6. The single-cell transcriptome of mTECs and CD4Frontiers in immunology · 2024
    Article
  7. Twenty Years of AIRE.Frontiers in immunology · 2018
    Review
  8. Article
  9. Article
  10. Article
  11. Thymic stromal cell subsets for T cell development.Cellular and molecular life sciences : CMLS · 2016
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. The many faces of aire in central tolerance.Frontiers in immunology · 2013
    Review
  20. Human APECED; a Sick Thymus Syndrome?Frontiers in immunology · 2013
    Review
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

3 authors at 1 institution in 1 country.

James DooleyDepartment of Biological Structure, University of Washington, Seattle, WA 98195, USA.
Matthew Erickson
Andrew G Farr
California Institute for Regenerative Medicine · US

Funding

Heterogeneity of medullary thymic epitheliumR01AI059575 · NIAID · UNIVERSITY OF WASHINGTON · PI FARR, ANDREW G · 2004 to 2010
$2.6M
NIAID NIH HHS AI09575NIAID NIH HHS R01 AI059575
6 · The paper itself

Abstract

A widely held model of thymic epithelial differentiation is based on patterns of keratin expression, where a K8(+)K5(+) progenitor gives rise to K8(+)K5/K14(-) cortical thymic epithelium (CTEC), and medullary thymic epithelium (MTEC) are K8(-)K5(+)K14(+). The thymic phenotype of p63-deficient mice indicates that p63 is an important regulator of proximal stages of thymic epithelial differentiation. In this study, we have examined several features of the thymic medullary compartment in wild-type and Aire-deficient thymi in an effort to integrate the proapoptotic activity of Aire with these different perspectives of TE differentiation. Patterns of keratin and p63 expression by MTEC described here are difficult to reconcile with postmitotic MTEC that express a K8(-)K14(+) phenotype and suggest that the patterns of p63 and keratin expression reflecting differentiation programs of other epithelial tissues provide a useful framework for revising models of TE differentiation. Alterations of the Aire(-/-) MTEC compartment included reduced expression of p63, increased frequency of MTEC expressing truncated Aire protein, and shifts in the pattern of keratin expression and epithelial morphology. These data suggest a scenario where cellular targets of Aire-mediated apoptosis are postmitotic MTEC that have not yet completed their terminal differentiation program. According to this view, the minor population of globular K8(+)K14(-/low) MTEC observed in the Aire(+/+) thymus and significantly expanded in the Aire(-/-) thymic medulla represent end-stage, terminally differentiated MTEC. These Aire-dependent alterations of the MTEC compartment suggest that the activity of Aire is not neutral with respect to the program of MTEC differentiation.

Indexed as

AIRE ProteinAnimalsApoptosisCell DifferentiationEpithelial CellsGene Expression RegulationKeratinsMiceMice, KnockoutPhosphoproteinsThymus GlandTrans-ActivatorsTranscription FactorsAIRE ProteinKeratinsPhosphoproteinsTrans-ActivatorsTranscription FactorsTrp63 protein, mouse

Identifiers

PMID18832676
PMCPMC2677919
OpenAlexW1950764505

What OpenQuestion 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 OpenQuestion graph.