Evidence map›Paper›PMID 23436244›Full record

ArticleEuropean journal of immunology2013

Polarity gene discs large homolog 1 regulates the generation of memory T cells.

Grzegorz B Gmyrek, Daniel B Graham, Gabriel J Sandoval, Gregory S Blaufuss, Holly M Akilesh, Keiko Fujikawa, Ramnik J Xavier, Wojciech Swat

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Grzegorz B GmyrekDivison of Immunobiology, Washington University School of Medicine, St Louis, MO 63110, USA.
Daniel B Graham
Gabriel J Sandoval
Gregory S Blaufuss
Holly M Akilesh
Keiko Fujikawa
Ramnik J Xavier
Wojciech Swat
Washington University in St. Louis · USCenter for Systems Biology · USHokkaido University of Science · JP

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Ramnik J Xavier · 1991 to 2026
$35.3M
Vav Family Proteins in T Lymphocyte ActivationR01AI061077 · NIAID · WASHINGTON UNIVERSITY · PI SWAT, WOJCIECH A · 2004 to 2008
$1.9M
Role of Carma1 in Inflammatory Lung DiseaseR01HL088297 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MEDOFF, BENJAMIN DAVID, XAVIER, RAMNIK J · 2008 to 2011
$1.6M
DLGH1 AND UROGENITAL DEVELOPMENTR01DK081156 · NIDDK · WASHINGTON UNIVERSITY · PI MINER, JEFFREY H, SWAT, WOJCIECH A · 2008 to 2012
$1.6M
MECHANISMS OF SIGNALING BY ACTIVATING RECEPTORS IN INNATE IMMUNE SYSTEMS CELLSR01AI073718 · NIAID · WASHINGTON UNIVERSITY · PI SWAT, WOJCIECH A · 2009 to 2010
$760k
NHLBI NIH HHS HL088297NHLBI NIH HHS R01 HL088297NIAID NIH HHS R01 AI061077NIAID NIH HHS R01AI061077NIAID NIH HHS R01 AI073718NIAID NIH HHS R01AI073718NIDDK NIH HHS DK043351NIDDK NIH HHS P30 DK043351NIDDK NIH HHS R01 DK081156
6 · The paper itself

Abstract

Mammalian ortholog of Drosophila cell polarity protein, Dlg1, plays a critical role in neural synapse formation, epithelial cell homeostasis, and urogenital development. More recently, it has been proposed that Dlg1 may also be involved in the regulation of T-cell proliferation, migration, and Ag-receptor signaling. However, a requirement for Dlg1 in development and function of T lineage cells remains to be established. In this study, we investigated a role for Dlg1 during T-cell development and function using a combination of conditional Dlg1 KO and two different Cre expression systems where Dlg1 deficiency is restricted to the T-cell lineage only, or all hematopoietic cells. Here, using three different TCR models, we show that Dlg1 is not required during development and selection of thymocytes bearing functionally rearranged TCR transgenes. Moreover, Dlg1 is dispensable in the activation and proliferative expansion of Ag-specific TCR-transgenic CD4(+) and CD8(+) T cells in vitro and in vivo. Surprisingly, however, we show that Dlg1 is required for normal generation of memory T cells during endogenous response to cognate Ag. Thus, Dlg1 is not required for the thymocyte selection or the activation of primary T cells, however it is involved in the generation of memory T cells.

Indexed as

Immunologic MemoryAdoptive TransferAnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationCell LineageCell PolarityCell ProliferationDiscs Large Homolog 1 ProteinGene ExpressionIntegrasesMiceMice, KnockoutNerve Tissue ProteinsOvalbuminCre recombinaseDiscs Large Homolog 1 ProteinDlg1 protein, mouseIntegrasesNerve Tissue ProteinsOvalbuminReceptors, Antigen, T-CellSAP90-PSD95 Associated Proteins

Identifiers

PMID23436244
PMCPMC3894631
OpenAlexW1919045686

What Socratic 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 Socratic graph.