Evidence map›Paper›PMID 22323537›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Cutting edge: the "death" adaptor CRADD/RAIDD targets BCL10 and suppresses agonist-induced cytokine expression in T lymphocytes.

Qing Lin, Yan Liu, Daniel J Moore, Sydney K Elizer, Ruth A Veach, Jacek Hawiger, H Earl Ruley

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. The role of the CBM complex in allergic inflammation and disease.The Journal of allergy and clinical immunology · 2022
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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

7 authors at 1 institution in 1 country.

Qing LinDepartment of Microbiology and Immunology, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.
Yan Liu
Daniel J Moore
Sydney K Elizer
Ruth A Veach
Jacek Hawiger
H Earl Ruley
Vanderbilt University · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MATTHEW J TYSKA · 1995 to 2026
$172.8M
T Lymphocyte based functional genomics of inflammationP01HL068744 · NHLBI · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2002 to 2006
$9.9M
Superantigen-Induced Vascular Injury and DICR01HL069452 · NHLBI · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2001 to 2011
$3.3M
Intracellular Therapeutics for Inflammatory Liver InjuryR01AA015752 · NIAAA · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2007 to 2011
$1.7M
Targeted Suppression of Cytokine Signaling in the Acute Phase ResponseR01HL085833 · NHLBI · VANDERBILT UNIVERSITY · PI HAWIGER, JACK J · 2008 to 2011
$1.5M
Harnessing B lymphocytes as Antigen-Specific Regulators of Islet ToleranceK08DK090146 · NIDDK · VANDERBILT UNIVERSITY · PI MOORE, DANIEL J. · 2011 to 2013
$434k
NCI NIH HHS P30 CA068485NCI NIH HHS P30CA68485NHLBI NIH HHS HL069452NHLBI NIH HHS HL085833NHLBI NIH HHS HL687440NHLBI NIH HHS P01 HL068744NHLBI NIH HHS R01 HL069452NHLBI NIH HHS R01 HL085833NIAAA NIH HHS AA015752NIAAA NIH HHS R01 AA015752NIDDK NIH HHS 1KO8 DK090146NIDDK NIH HHS K08 DK090146NIDDK NIH HHS L40 DK084746
6 · The paper itself

Abstract

The expression of proinflammatory cytokines and chemokines in response to TCR agonists is regulated by the caspase-recruitment domain membrane-associated guanylate kinase 1 (CARMA1) signalosome through the coordinated assembly of complexes containing the BCL10 adaptor protein. We describe a novel mechanism to negatively regulate the CARMA1 signalosome by the "death" adaptor protein caspase and receptor interacting protein adaptor with death domain (CRADD)/receptor interacting protein-associated ICH-1/CED-3 homologous protein with a death domain. We show that CRADD interacts with BCL10 through its caspase recruitment domain and suppresses interactions between BCL10 and CARMA1. TCR agonist-induced interaction between CRADD and BCL10 coincides with reduction of its complex formation with CARMA1 in wild-type, as compared with Cradd-deficient, primary cells. Finally, Cradd-deficient spleen cells, CD4(+) T cells, and mice respond to T cell agonists with strikingly higher production of proinflammatory mediators, including IFN-γ, IL-2, TNF-α, and IL-17. These results define a novel role for CRADD as a negative regulator of the CARMA1 signalosome and suppressor of Th1- and Th17-mediated inflammatory responses.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsB-Cell CLL-Lymphoma 10 ProteinCARD Signaling Adaptor ProteinsCD4-Positive T-LymphocytesCell SeparationCRADD Signaling Adaptor ProteinFlow CytometryImmunoblottingImmunoprecipitationLymphocyte ActivationMiceMice, Inbred C57BLSignal TransductionAdaptor Proteins, Signal TransducingB-Cell CLL-Lymphoma 10 ProteinBcl10 protein, mouseCard11 protein, mouseCARD Signaling Adaptor ProteinsCradd protein, mouseCRADD Signaling Adaptor Protein

Identifiers

PMID22323537
PMCPMC3294148
OpenAlexW2127725635

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.