Evidence map›Paper›PMID 26408667›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Differential Requirements of TCR Signaling in Homeostatic Maintenance and Function of Dendritic Epidermal T Cells.

Baojun Zhang, Jianxuan Wu, Yiqun Jiao, Cheryl Bock, Meifang Dai, Benny Chen, Nelson Chao, Weiguo Zhang, Yuan Zhuang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

46 citing papers in PubMed, 61 citations in OpenAlex.

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  16. Development of γδ T Cells: Soldiers on the Front Lines of Immune Battles.Methods in molecular biology (Clifton, N.J.) · 2023
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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

9 authors at 2 institutions in 1 country.

Baojun ZhangDepartment of Immunology, Duke University Medical Center, Durham, NC 27710;
Jianxuan WuDepartment of Immunology, Duke University Medical Center, Durham, NC 27710;
Yiqun JiaoDepartment of Medicine, Duke University Medical Center, Durham, NC 27710; and.
Cheryl BockDuke Cancer Institute, Duke University Medical Center, Durham, NC 27710.
Meifang DaiDepartment of Immunology, Duke University Medical Center, Durham, NC 27710;
Benny ChenDepartment of Medicine, Duke University Medical Center, Durham, NC 27710; and.
Nelson ChaoDepartment of Immunology, Duke University Medical Center, Durham, NC 27710; Department of Medicine, Duke University Medical Center, Durham, NC 27710; and Duke Cancer Institute, Duke University Medical Center, Durham, NC 27710.
Weiguo ZhangDepartment of Immunology, Duke University Medical Center, Durham, NC 27710; Duke Cancer Institute, Duke University Medical Center, Durham, NC 27710.
Yuan ZhuangDepartment of Immunology, Duke University Medical Center, Durham, NC 27710; Duke Cancer Institute, Duke University Medical Center, Durham, NC 27710 yzhuang@duke.edu.
Duke Medical Center · USDuke University Hospital · US

Funding

The role of TCR, ligand, and signal strength in human γδ T cell developmentP01AI102853 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI CORNELIS MURRE · 2014 to 2026
$26.3M
HEB MEDIATED PATHWAYS AND FUNCTION IN T CELL DEVELOPMENTR01GM059638 · NIGMS · DUKE UNIVERSITY · PI CHAN, FRANCIS KAMING · 1999 to 2021
$6.9M
A new approach to homeostatic maintenance of dendritic epidermal T cellsR21AG045440 · NIA · DUKE UNIVERSITY · PI ZHUANG, YUAN · 2014 to 2015
$428k
A New Genetic Tool for Lineage Tracing of Mitotic Cells in MiceR21RR032742 · NCRR · DUKE UNIVERSITY · PI ZHUANG, YUAN · 2011 to 2011
$236k
NCRR NIH HHS R21 RR032742NCRR NIH HHS R21RR-032742NIAID NIH HHS P01 AI102853NIAID NIH HHS P01AI102853NIA NIH HHS R21 AG045440NIA NIH HHS R21AG-045440NIGMS NIH HHS R01 GM059638NIGMS NIH HHS R01GM-059638,
6 · The paper itself

Abstract

Dendritic epidermal T cells (DETCs) are generated exclusively in the fetal thymus and maintained in the skin epithelium throughout postnatal life of the mouse. DETCs have restricted antigenic specificity as a result of their exclusive usage of a canonical TCR. Although the importance of the TCR in DETC development has been well established, the exact role of TCR signaling in DETC homeostasis and function remains incompletely defined. In this study, we investigated TCR signaling in fully matured DETCs by lineage-restricted deletion of the Lat gene, an essential signaling molecule downstream of the TCR. We found that Lat deletion impaired TCR-dependent cytokine gene activation and the ability of DETCs to undergo proliferative expansion. However, linker for activation of T cells-deficient DETCs were able to maintain long-term population homeostasis, although with a reduced proliferation rate. Mice with Lat deletion in DETCs exhibited delayed wound healing accompanied by impaired clonal expansion within the wound area. Our study revealed differential requirements for TCR signaling in homeostatic maintenance of DETCs and in their effector function during wound healing.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsAnimals, NewbornCells, CulturedFlow CytometryHomeostasisLangerhans CellsLuminescent ProteinsMembrane ProteinsMice, KnockoutMice, TransgenicMicroscopy, ConfocalPhosphoproteinsReceptors, Antigen, T-CellSignal TransductionT-LymphocytesAdaptor Proteins, Signal TransducingLat protein, mouseLuminescent ProteinsMembrane ProteinsPhosphoproteinsReceptors, Antigen, T-Cell

Identifiers

PMID26408667
PMCPMC4610875
OpenAlexW2283827431

What OpenQuestion 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 OpenQuestion graph.