Evidence map›Paper›PMID 27088444›Full record

ArticleNature communications2016

Ndfip-mediated degradation of Jak1 tunes cytokine signalling to limit expansion of CD4+ effector T cells.

Claire E O'Leary, Christopher R Riling, Lynn A Spruce, Hua Ding, Suresh Kumar, Guoping Deng, Yuhong Liu, Steven H Seeholzer, Paula M Oliver

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

25 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  5. Review
  6. Review
  7. Article
  8. EHBP1L1 Drives Immune Evasion in Renal Cell Carcinoma through Binding and Stabilizing JAK1.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  9. Article
  10. Review
  11. Article
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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 3 institutions in 1 country.

Claire E O'LearyPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Christopher R RilingPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Lynn A SpruceDepartment of Pathology and Laboratory Medicine, Cell Pathology Division, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Hua DingDepartment of Pathology and Laboratory Medicine, Cell Pathology Division, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Suresh KumarProgenra Inc, Malvern, Pennsylvania, 19355, USA.ORCID http://orcid.org/0000-0002-1940-772X
Guoping DengDepartment of Pathology and Laboratory Medicine, Cell Pathology Division, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Yuhong LiuDepartment of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Steven H SeeholzerDepartment of Pathology and Laboratory Medicine, Cell Pathology Division, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
Paula M OliverPerelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · USProgenra (United States) · US

Funding

TRAINING PROGRAM IN CELL AND MOLECULAR BIOLOGYT32GM007229 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BARTOLOMEI, MARISA S. · 1985 to 2023
$14.0M
Mechanisms of ubiquitin pathway activation and functionR01AI114515 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI OLIVER, PAULA MARIA · 2015 to 2019
$2.1M
NIAID NIH HHS R01 AI114515NIGMS NIH HHS T32 GM007229
6 · The paper itself

Abstract

Nedd4 family E3 ubiquitin ligases have been shown to restrict T-cell function and impact T-cell differentiation. We show here that Ndfip1 and Ndfip2, activators of Nedd4 family ligases, together limit accumulation and function of effector CD4+ T cells. Using a three-part proteomics approach in primary T cells, we identify stabilization of Jak1 in Ndfip1/2-deficient T cells stimulated through the TCR. Jak1 degradation is aborted in activated T cells that lack Ndfips. In wild-type cells, Jak1 degradation lessens CD4+ cell sensitivity to cytokines during TCR stimulation, while in Ndfip-deficient cells cytokine responsiveness persists, promoting increased expansion and survival of pathogenic effector T cells. Thus, Ndfip1/Ndfip2 regulate the cross talk between the T-cell receptor and cytokine signalling pathways to limit inappropriate T-cell responses.

Indexed as

Signal TransductionAnimalsCarrier ProteinsCD4-Positive T-LymphocytesCell ProliferationCells, CulturedColitisCytokinesFemaleImmunoblottingIntercellular Signaling Peptides and ProteinsJanus Kinase 1Lymphocyte CountMaleMembrane ProteinsMice, Inbred C57BLCarrier ProteinsCytokinesIntercellular Signaling Peptides and ProteinsJak1 protein, mouseJanus Kinase 1Membrane ProteinsNdfip1 protein, mouseNDFIP2 protein, mouse

Identifiers

PMID27088444
PMCPMC4837450
OpenAlexW2337009973

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.