Evidence map›Paper›PMID 18342008›Full record

ArticleImmunity2008

Complementation in trans of altered thymocyte development in mice expressing mutant forms of the adaptor molecule SLP76.

Martha S Jordan, Jennifer E Smith, Jeremy C Burns, Jessica-Elise T Austin, Kim E Nichols, Anna C Aschenbrenner, Gary A Koretzky

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

72 citing papers in PubMed, 104 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Tuning T helper cell differentiation by ITK.Biochemical Society transactions · 2020
    Review
  7. Article
  8. Review
  9. Article
  10. ERK Signaling Controls Innate-like CD8Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  11. Id3 Restricts γδ NKT Cell Expansion by Controlling Egr2 and c-Myc Activity.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  12. IL-4 and IL-15 promotion of virtual memory CD8European journal of immunology · 2016
    Article
  13. TCR signaling by conventional CD4Immunity, inflammation and disease · 2016
    Article
  14. NFAT2 Regulates Generation of Innate-Like CD8Frontiers in immunology · 2016
    Article
  15. Article
  16. Article
  17. Thymic low affinity/avidity interaction selects natural Th1 cells.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  18. Regulatory T cells require TCR signaling for their suppressive function.Journal of immunology (Baltimore, Md. : 1950) · 2015
    Article
  19. Article
  20. Review

12 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

7 authors at 4 institutions in 2 countries.

Martha S JordanCancer Biology, Abramson Family Cancer Research Institute, 427 BRBII/III, University of Pennsylvania School of Medicine, Philadelphia, PA, 19104, USA.
Jennifer E Smith
Jeremy C Burns
Jessica-Elise T Austin
Kim E Nichols
Anna C Aschenbrenner
Gary A Koretzky
Cancer Research Institute · USChildren's Hospital of Philadelphia · USUniversity of Bonn · DEUniversity of Pennsylvania · US

Funding

The Function of Tribbles in the Pathogenesis of AMLP01CA093615 · NCI · UNIVERSITY OF PENNSYLVANIA · PI BIRNBAUM, MORRIS J · 2002 to 2011
$16.2M
Regulation of PMN activation by SLP-76, PRAM-1 and ADAPR01AI061039 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI KORETZKY, GARY A. · 2004 to 2008
$2.1M
NOVEL SUBSTRATES OF THE TCR KINASER01GM053256 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI KORETZKY, GARY A. · 1995 to 2005
$1.8M
TRAINING IN COMPARITIVE MEDICAL &MOLECULAR GENETICST32RR007063 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI WOLFE, JOHN H · 1996 to 2011
$1.8M
NCI NIH HHS P01 CA093615NCRR NIH HHS T32 RR007063NCRR NIH HHS T32-RR07063NIAID NIH HHS R01 AI061039NIGMS NIH HHS R01 GM053256
6 · The paper itself

Abstract

The adaptor protein SLP76 directs signaling downstream of the T cell receptor (TCR) and is essential for thymocyte development. SLP76 contains three N-terminal tyrosines that are critical for its function. To define the role of these residues in thymocyte development, we generated two lines of "knock-in" mice, one expressing a mutation in tyrosine 145 (Y145F) and a second harboring two point mutations at tyrosines 112 and 128 (Y112-128F). We show here that although thymocyte development requires both Y145- and Y112-128-generated signals, selection was more dependent upon Y145. Although several proximal TCR signaling events were defective in both mutant mice, phosphorylation of the guanine nucleotide exchange factor, Vav1, and activation of Itk-dependent pathways were differentially affected by mutations at Y112-128 and Y145, respectively. Analysis of mice expressing one Y145F and one Y112-128F allele revealed that these mutants could complement one another in trans, demonstrating cooperativity between two or more SLP76 molecules. Thus, the N-terminal tyrosines of SLP76 are required for thymocyte selection but can function on separate molecules to support TCR signaling.

Indexed as

Adaptor Proteins, Signal TransducingAmino Acid SequenceAnimalsCell DifferentiationFlow CytometryImmunoblottingImmunoprecipitationMiceMice, Mutant StrainsMutationPhosphoproteinsReceptors, Antigen, T-CellReverse Transcriptase Polymerase Chain ReactionSignal TransductionT-LymphocytesTyrosineAdaptor Proteins, Signal TransducingPhosphoproteinsReceptors, Antigen, T-CellSLP-76 signal Transducing adaptor proteinsTyrosine

Identifiers

PMID18342008
PMCPMC2323515
OpenAlexW2059623963

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.