Evidence map›Paper›PMID 18434124›Full record

ReviewCurrent opinion in immunology2008

Notch signaling in CD4 and CD8 T cell development.

Karen Laky, B J Fowlkes

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
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  6. Review
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  10. Review
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  13. Extracellular Vesicle-Contained microRNA ofFrontiers in cellular and infection microbiology · 2020
    Article
  14. Article
  15. CDK8-Novel Therapeutic Opportunities.Pharmaceuticals (Basel, Switzerland) · 2019
    Review
  16. Article
  17. Review
  18. Tangeretin has anti-asthmatic effects via regulating PI3K and Notch signaling and modulating Th1/Th2/Th17 cytokine balance in neonatal asthmatic mice.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2017
    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

2 authors at 1 institution in 1 country.

Karen LakyLaboratory of Cellular and Molecular Immunology, NIAID, National Institutes of Health, Bethesda, MD 20892-0420, USA. klaky@niaid.nih.gov
B J Fowlkes
National Institutes of Health · US

Funding

T Cell DifferentiationZIAAI000486 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FOWLKES, B. · 2009 to 2015
$8.5M
T CELL DIFFERENTIATIONZ01AI000486 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI FOWLKES, BJ · 1987 to 2008
$3.6M
Intramural NIH HHS Z01 AI000486
6 · The paper itself

Abstract

Because Notch often acts in concert with other signaling pathways, it is able to regulate a diverse set of biological processes in a cell-context dependent manner. In lymphocytes, Notch is essential for specifying the T cell fate and for promoting early stages of T cell differentiation. At later stages of development, Notch signaling is proposed to direct CD4 versus CD8 T lineage commitment. This hypothesis has been challenged by recent studies of conditional Presenilin-deficient mice showing that Notch promotes the selection and maturation of CD4 and CD8 T cells by potentiating TCR signal transduction in immature thymocytes. While similar conclusions have not been reported with conditional mutation of other downstream mediators of Notch activation, it appears that functional inhibition may not have been achieved at a comparable stage of development and/or analogous issues have not been addressed. The differences also question whether in thymocytes Notch signals only through the canonical pathway. Further study of conditional mutants, signaling intermediates, and transcriptional regulators are needed to elucidate how Notch facilitates TCR signaling in generating mature T cells.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell LineageMiceReceptors, Antigen, T-CellReceptors, NotchSignal TransductionThymus GlandReceptors, Antigen, T-CellReceptors, Notch

Identifiers

PMID18434124
PMCPMC2475578
OpenAlexW2003730490

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.