Evidence map›Paper›PMID 15795236›Full record

ArticleThe Journal of experimental medicine2005

Mutation of the phospholipase C-gamma1-binding site of LAT affects both positive and negative thymocyte selection.

Connie L Sommers, Jan Lee, Kevin L Steiner, Jordan M Gurson, Corinne L Depersis, Dalal El-Khoury, Claudette L Fuller, Elizabeth W Shores, Paul E Love, Lawrence E Samelson

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

50 citing papers in PubMed, 80 citations in OpenAlex.

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  4. T cell receptor (TCR) signaling in health and disease.Signal transduction and targeted therapy · 2021
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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 3 institutions in 2 countries.

Connie L SommersLaboratory of Cellular and Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Jan Lee
Kevin L Steiner
Jordan M Gurson
Corinne L Depersis
Dalal El-Khoury
Claudette L Fuller
Elizabeth W Shores
Paul E Love
Lawrence E Samelson
Cancer Institute (WIA) · INNational Institutes of Health · USCenter for Biologics Evaluation and Research · US

Funding

Genes and signals controlling mammalian hematopoiesis.ZIAHD001803 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI LOVE, PAUL E · 2009 to 2025
$36.9M
Biochemical Basis of T Cell ActivationZIABC010304 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SAMELSON, LAWRENCE · 2009 to 2025
$36.3M
BIOCHEMICAL BASIS OF T CELL ACTIVATIONZ01BC010304 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SAMELSON, LAWRENCE E · 1999 to 2008
$2.6M
Signals Regulating T Cell DevelopmentZ01HD001803 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI LOVE, PAUL E · 1994 to 2008
$2.2M
Intramural NIH HHS Z01 BC010304NCI NIH HHS Z01 BC010304-07
6 · The paper itself

Abstract

Linker for activation of T cells (LAT) is a scaffolding adaptor protein that is critical for T cell development and function. A mutation of LAT (Y136F) that disrupts phospholipase C-gamma1 activation and subsequent calcium influx causes a partial block in T cell development and leads to a severe lymphoproliferative disease in homozygous knock-in mice. One possible contribution to the fatal disease of LAT Y136F knock-in mice could be from autoreactive T cells generated in these mice because of altered thymocyte selection. To examine the impact of the LAT Y136F mutation on thymocyte positive and negative selection, we bred this mutation onto the HY T cell receptor (TCR) transgenic, recombination activating gene-2 knockout background. Female mice with this genotype showed a severe defect in positive selection, whereas male mice exhibited a phenotype resembling positive selection (i.e., development and survival of CD8(hi) HY TCR-specific T cells) instead of negative selection. These results support the hypothesis that in non-TCR transgenic, LAT Y136F knock-in mice, altered thymocyte selection leads to the survival and proliferation of autoreactive T cells that would otherwise be negatively selected in the thymus.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsApoptosisBinding SitesCalciumCell ProliferationDNA PrimersEnzyme-Linked Immunosorbent AssayFlow CytometryLymphoproliferative DisordersMembrane ProteinsMiceMice, Inbred C57BLMice, Mutant StrainsMuscle ProteinsMutationAdaptor Proteins, Signal TransducingCalciumDNA PrimersLat protein, mouseMembrane ProteinsMuscle ProteinsPhospholipase C gammaPhosphoproteinsPlcg1 protein, mouseReceptors, Antigen, T-CellType C Phospholipases

Identifiers

PMID15795236
PMCPMC1538971
OpenAlexW2096613461

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.