Evidence map›Paper›PMID 22810897›Full record

ArticleScience signaling2012

Abl family kinases modulate T cell-mediated inflammation and chemokine-induced migration through the adaptor HEF1 and the GTPase Rap1.

Jing Jin Gu, Catherine P Lavau, Elena Pugacheva, Erik J Soderblom, M Arthur Moseley, Ann Marie Pendergast

Abstract read
In one paragraph

Article in Science signaling, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 46 citations in OpenAlex.

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  7. Ponatinib and other CML Tyrosine Kinase Inhibitors in Thrombosis.International journal of molecular sciences · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Jing Jin GuDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC 27710, USA.
Catherine P Lavau
Elena Pugacheva
Erik J Soderblom
M Arthur Moseley
Ann Marie Pendergast
Duke University · USWest Virginia University · US

Funding

Role of Abl Kinases in immune cell signalingR01AI056266 · NIAID · DUKE UNIVERSITY · PI PENDERGAST, ANN MARIE · 2004 to 2015
$3.6M
MOLECULAR BASIS OF SIGNALING BY THE CABL PROTO-ONCOGENER01CA070940 · NCI · DUKE UNIVERSITY · PI PENDERGAST, ANN MARIE · 1996 to 2010
$3.4M
The role of HEF1 protein in division and invasion of metastatic breast cancerR01CA148671 · NCI · WEST VIRGINIA UNIVERSITY · PI PUGACHEVA, ELENA NIKOLAEVNA · 2010 to 2020
$3.2M
Kinase Target of Diverse Cell Surface Receptors in Cancer Invasion and MetastasisR01CA155160 · NCI · DUKE UNIVERSITY · PI PENDERGAST, ANN MARIE · 2011 to 2015
$1.6M
NCI NIH HHS CA070940NCI NIH HHS CA148671NCI NIH HHS CA155160NCI NIH HHS R01 CA070940NCI NIH HHS R01 CA148671NCI NIH HHS R01 CA155160NIAID NIH HHS AI056266NIAID NIH HHS R01 AI056266
6 · The paper itself

Abstract

Chemokine signaling is critical for T cell function during homeostasis and inflammation and directs T cell polarity and migration through the activation of specific intracellular pathways. Here, we uncovered a previously uncharacterized role for the Abl family tyrosine kinases Abl and Arg in the regulation of T cell-dependent inflammatory responses and showed that the Abl family kinases were required for chemokine-induced T cell polarization and migration. Our data demonstrated that Abl and Arg were activated downstream of chemokine receptors and mediated the chemokine-induced tyrosine phosphorylation of human enhancer of filamentation 1 (HEF1), an adaptor protein that is required for the activity of the guanosine triphosphatase Rap1, which mediates cell adhesion and migration. Phosphorylation of HEF1 by Abl family kinases and activation of Rap1 were required for chemokine-induced T cell migration. Mouse T cells that lacked Abl and Arg exhibited defective homing to lymph nodes and impaired migration to sites of inflammation. These findings suggest that Abl family kinases are potential therapeutic targets for the treatment of T cell-dependent immune disorders that are characterized by chemokine-mediated inflammation.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBlotting, WesternCell AdhesionCell MovementChemokinesGuanosine TriphosphateHumansInflammationMicePhosphoproteinsPhosphorylationProtein-Tyrosine KinasesSignal TransductionTime-Lapse ImagingT-LymphocytesAdaptor Proteins, Signal TransducingARG tyrosine kinaseChemokinesGuanosine TriphosphateNEDD9 protein, humanPhosphoproteinsProtein-Tyrosine Kinases

Identifiers

PMID22810897
PMCPMC3602906
OpenAlexW2050871600

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.