Evidence map›Paper›PMID 21136199›Full record

ReviewImmunologic research2011

A tale of two TRAPs: LAT and LAB in the regulation of lymphocyte development, activation, and autoimmunity.

Deirdre M Fuller, Minghua Zhu, Chih-Wen Ou-Yang, Sarah A Sullivan, Weiguo Zhang

Abstract readReview
In one paragraph

Review in Immunologic research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Deirdre M FullerDepartment of Immunology, Duke University Medical Center, Durham, NC 27710, USA.
Minghua Zhu
Chih-Wen Ou-Yang
Sarah A Sullivan
Weiguo Zhang
Duke Medical Center · USDuke University · US

Funding

Analysis of adaptor protein (LAT) in TCR signalingR01AI048674 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2001 to 2011
$3.5M
Phospholipase D proteins in immunoreceptor-mediated signalingR01AI093717 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2011 to 2015
$1.9M
Adaptor molecules in lymphocyte signalingR01AI056156 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2003 to 2007
$1.5M
Analysis of adaptor protein (LAT) in TCR signalingR56AI048674 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2012 to 2012
$385k
Adaptor molecules in lymphocyte signalingR56AI056156 · NIAID · DUKE UNIVERSITY · PI ZHANG, WEIGUO · 2010 to 2010
$382k
NIAID NIH HHS AI048674NIAID NIH HHS AI056156NIAID NIH HHS R01 AI048674NIAID NIH HHS R01 AI056156NIAID NIH HHS R01 AI093717NIAID NIH HHS R56 AI048674NIAID NIH HHS R56 AI056156
6 · The paper itself

Abstract

Transmembrane adaptor proteins (TRAPs) link antigen receptor engagement to downstream cellular processes. Although these proteins typically lack intrinsic enzymatic activity, they are phosphorylated on multiple tyrosine residues following lymphocyte activation, allowing them to function as scaffolds for the assembly of multi-molecular signaling complexes. Among the many TRAPs that have been discovered in recent years, the LAT (linker for activation of T cells) family of adaptor proteins plays an important role in the positive and negative regulation of lymphocyte maturation, activation, and differentiation. Of the two members in this family, LAT is an indispensable component controlling T cell and mast cell activation and function; LAB (linker for activation of B cells), also called NTAL, is necessary to fine-tune lymphocyte activation and may be a key regulator of innate immune responses. Here, we review recent advances on the function of LAT and LAB in the regulation of development and activation of immune cells.

Indexed as

AutoimmunityLymphocyte ActivationAdaptor Proteins, Signal TransducingAnimalsCell DifferentiationHumansMembrane ProteinsT-LymphocytesAdaptor Proteins, Signal TransducingLAT2 protein, humanLAT protein, humanMembrane Proteins

Identifiers

PMID21136199
PMCPMC3646367
OpenAlexW2109837993

What Socratic 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 Socratic graph.