Evidence map›Paper›PMID 18511409›Full record

ArticleInternational immunology2008

ICAT expression disrupts beta-catenin-TCF interactions and impairs survival of thymocytes and activated mature T cells.

M Zulfiquer Hossain, Qing Yu, Mai Xu, Jyoti Misra Sen

Open access · greenAbstract read
In one paragraph

Article in International immunology, 2008. 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
1.9field-weighted citation impact, top 14% 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, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Long noncoding RNAAutophagy · 2020
    Article
  5. Article
  6. Article
  7. Article
  8. Wnt Signaling: Role in Regulation of Haematopoiesis.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2016
    Review
  9. Article
  10. β-catenin/TCF-1 pathway in T cell development and differentiation.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2012
    Review
  11. Review
  12. Article
  13. Article
  14. Wnt/beta-catenin signaling in T-cell immunity and cancer immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2010
    Review
  15. Beta-catenin signaling mediates CD4 expression on mature CD8+ T cells.Journal of immunology (Baltimore, Md. : 1950) · 2010
    Article
  16. Review
  17. Article
  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

4 authors at 1 institution in 1 country.

M Zulfiquer HossainLymphocyte Development Unit, Laboratory of Immunology, National Institute on Aging, National Institutes of Health, 5600 Nathan Shock Drive, Baltimore, MD 21224, USA.
Qing Yu
Mai Xu
Jyoti Misra Sen
National Institutes of Health · US

Funding

T cell development in the thymus and age-dependent thymic involutionZIAAG000768 · NIA · NATIONAL INSTITUTE ON AGING · PI EGAN, JOSEPHINE · 2009 to 2025
$4.0M
Signal Transduction in T cell development, function and agingZ01AG000768 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, JYOTI · 2004 to 2008
$1.5M
Beta-Catenin in T Cell FunctionZ01AG000772 · NIA · NATIONAL INSTITUTE ON AGING · PI SEN, JYOTI · 2008 to 2008
$224k
Intramural NIH HHS Z01 AG000768
6 · The paper itself

Abstract

T cell factor (TCF) family of transcription factors and beta-catenin critically regulate T cell development as demonstrated by the deletion of the tcf gene, which results in a block early in development that becomes complete in mice bearing tcf/lef double deletion. However, the role of beta-catenin, a major TCF cofactor, remains controversial. To directly address this, we have generated transgenic mice expressing Inhibitor of beta-catenin and TCF (ICAT), a naturally occurring inhibitor that specifically disrupts TCF and beta-catenin interactions. In this report, we demonstrate that disrupting the interaction of beta-catenin with TCF renders adult thymocytes and activated T cells highly susceptible to apoptosis. In contrast to previously reported observations during fetal thymocyte development, these data show that in adult mice, survival and not differentiation of thymocytes, depends on transcription by TCF and beta-catenin. Indeed, we demonstrate that expression of ICAT impedes thymocyte survival by reducing the expression of Bcl(xL) in thymocytes below a critical threshold. Survival of activated mature T cells was also impaired due to diminished expression of activation-induced Bcl(xL). Accordingly, expression of transgenic Bcl-2 rescued activated ICAT-Tg CD4 T cells from apoptosis. Thus, disruption of TCF-beta-catenin interactions specifically impairs the survival of thymocytes and activated T cells.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsApoptosisbcl-X Proteinbeta CateninCD4-Positive T-LymphocytesCell CountCell Cycle ProteinsCell SurvivalGene Expression RegulationImmunophenotypingMiceMice, Inbred C57BLMice, TransgenicProto-Oncogene Proteins c-bcl-2Repressor ProteinsAdaptor Proteins, Signal Transducingbcl-X Proteinbeta CateninCell Cycle ProteinsCtnnbip1 protein, mouseProto-Oncogene Proteins c-bcl-2Repressor ProteinsTCF Transcription FactorsTranscription Factors

Identifiers

PMID18511409
PMCPMC2556852
OpenAlexW2106188043

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.