Evidence map›Paper›PMID 25153088›Full record

ArticlePloS one2014

Unexpected phenotype of mice lacking Shcbp1, a protein induced during T cell proliferation.

Monica W Buckley, Sanja Arandjelovic, Paul C Trampont, Taeg S Kim, Thomas J Braciale, Kodi S Ravichandran

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.1field-weighted citation impact, top 47% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Visualizing the activation of encephalitogenic T cells in the ileal lamina propria by in vivo two-photon imaging.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. 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

6 authors at 1 institution in 1 country.

Monica W BuckleyDepartment of Microbiology, Immunology, Cancer biology, University of Virginia, Charlottesville, Virginia, United States of America; Carter Immunology Center, University of Virginia, Charlottesville, Virginia, United States of America; Center for Cell Clearance, University of Virginia, Charlottesville, Virginia, United States of America.
Sanja ArandjelovicDepartment of Microbiology, Immunology, Cancer biology, University of Virginia, Charlottesville, Virginia, United States of America; Carter Immunology Center, University of Virginia, Charlottesville, Virginia, United States of America; Center for Cell Clearance, University of Virginia, Charlottesville, Virginia, United States of America.
Paul C TrampontDepartment of Microbiology, Immunology, Cancer biology, University of Virginia, Charlottesville, Virginia, United States of America; Carter Immunology Center, University of Virginia, Charlottesville, Virginia, United States of America; Center for Cell Clearance, University of Virginia, Charlottesville, Virginia, United States of America.
Taeg S KimCenter for Cell Clearance, University of Virginia, Charlottesville, Virginia, United States of America.
Thomas J BracialeCenter for Cell Clearance, University of Virginia, Charlottesville, Virginia, United States of America.
Kodi S RavichandranDepartment of Microbiology, Immunology, Cancer biology, University of Virginia, Charlottesville, Virginia, United States of America; Carter Immunology Center, University of Virginia, Charlottesville, Virginia, United States of America; Center for Cell Clearance, University of Virginia, Charlottesville, Virginia, United States of America.
University of Virginia · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007267 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI GARCIA-BLANCO, MARIANO A. · 1985 to 2024
$13.4M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007496 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Michael G. Brown, Coleen A McNamara · 1995 to 2026
$10.2M
CYTOTOXIC T LYMPHOCYTE RESPONSE TO INFLUENZA VIRUSR01AI015608 · NIAID · WASHINGTON UNIVERSITY · PI BRACIALE, THOMAS J · 1985 to 2017
$5.7M
SIGNALING VIA SHC AND THE INOSITOL PHOSPHATASE, SHIPR01GM055761 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI RAVICHANDRAN, KODI S · 1998 to 2011
$3.2M
Role of Shcbp1 (mPAL) in T Cell Development and FunctionF30CA177173 · NCI · UNIVERSITY OF VIRGINIA · PI BUCKLEY, MONICA WEAVER · 2013 to 2015
$108k
NCI NIH HHS F30 CA177173NCI NIH HHS P30 CA044579NIAID NIH HHS R01 AI015608NIAID NIH HHS T32 AI007496NIGMS NIH HHS GM55761NIGMS NIH HHS R01 GM055761NIGMS NIH HHS T32 GM007267
6 · The paper itself

Abstract

T cell development and activation are highly regulated processes, and their proper execution is important for a competent immune system. Shc SH2-domain binding protein-1 (Shcbp1) is an evolutionarily conserved protein that binds to the adaptor protein ShcA. Studies in Drosophila and in cell lines have strongly linked Shcbp1 to cell proliferation, embryonic development, growth factor signaling, and tumorigenesis. Here we show that Shcbp1 expression is strikingly upregulated during the β-selection checkpoint in thymocytes, and that its expression tightly correlates with proliferative stages of T cell development. To evaluate the role for Shcbp1 during thymic selection and T cell function in vivo, we generated mice with global and conditional deletion of Shcbp1. Surprisingly, the loss of Shcbp1 expression did not have an obvious effect during T cell development. However, in a mouse model of experimental autoimmune encephalomyelitis (EAE), which depends on CD4(+) T cell function and mimics multiple features of the human disease multiple sclerosis, Shcbp1 deficient mice had reduced disease severity and improved survival, and this effect was T cell intrinsic. These data suggest that despite the striking upregulation of Shcbp1 during T cell proliferation, loss of Shcbp1 does not directly affect T cell development, but regulates CD4(+) T cell effector function in vivo.

Indexed as

AnimalsCell ProliferationEncephalomyelitis, Autoimmune, ExperimentalMiceMice, KnockoutPhenotypeShc Signaling Adaptor ProteinsSignal TransductionThymus GlandT-LymphocytesShcbp1 protein, mouseShc Signaling Adaptor Proteins

Identifiers

PMID25153088
PMCPMC4143286
OpenAlexW2067141996

What OpenQuestion holds

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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.