Evidence map›Paper›PMID 23313588›Full record

ArticleImmunity2013

The transcription factor NFAT exhibits signal memory during serial T cell interactions with antigen-presenting cells.

Francesco Marangoni, Thomas T Murooka, Teresa Manzo, Edward Y Kim, Esteban Carrizosa, Natalie M Elpek, Thorsten R Mempel

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

105 citing papers in PubMed, 166 citations in OpenAlex.

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  15. Differential roles of kinetic on- and off-rates in T-cell receptor signal integration revealed with a modified Fab'-DNA ligand.Proceedings of the National Academy of Sciences of the United States of America · 2024
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45 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Francesco MarangoniThe Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital, Boston, MA 02114, USA.
Thomas T Murooka
Teresa Manzo
Edward Y Kim
Esteban Carrizosa
Natalie M Elpek
Thorsten R Mempel
Massachusetts General Hospital · USHarvard University · US

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
Visualizing Effects of Costimulation on Antiviral ImmunityP01AI078897 · NIAID · HARVARD MEDICAL SCHOOL · PI VON ANDRIAN, ULRICH H · 2008 to 2012
$12.1M
Multidisciplinary HIV Training ProgramT32AI007387 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Daniel R. Kuritzkes · 1990 to 2026
$8.8M
Research Training in Rheumatology at Massachusetts General HospitalT32AR007258 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI ANDREW D LUSTER · 1986 to 2026
$6.9M
Migratory Properties of HIV-infected T cells in vivoR01AI097052 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MEMPEL, THORSTEN ROMAN · 2013 to 2016
$2.5M
Regulatory Immune Cell Networks in CancerR01CA150975 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MEMPEL, THORSTEN ROMAN · 2010 to 2014
$1.7M
Migratory Properties of HIV-infected T Cells in VivoR56AI097052 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MEMPEL, THORSTEN ROMAN · 2011 to 2011
$601k
Local regulation of cytotoxic T cell function in the tumor stromaR00AI073457 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MEMPEL, THORSTEN ROMAN · 2008 to 2009
$498k
Local regulation of cytotoxic T cell function in the tumor stromaK99AI073457 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MEMPEL, THORSTEN ROMAN · 2007 to 2007
$90k
NCI NIH HHS CA150975NCI NIH HHS R01 CA150975NIAID NIH HHS AI0178897NIAID NIH HHS AI073457NIAID NIH HHS AI097052NIAID NIH HHS K99 AI073457NIAID NIH HHS P01 AI078897NIAID NIH HHS R00 AI073457NIAID NIH HHS R01 AI097052NIAID NIH HHS R56 AI097052NIAID NIH HHS T32 AI007387NIAMS NIH HHS T32 AR007258NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

Interactions with antigen-presenting cells (APCs) interrupt T cell migration through tissues and trigger signaling pathways that converge on the activation of transcriptional regulators, including nuclear factor of activated T cells (NFAT), which control T cell function and differentiation. Both stable and unstable modes of cognate T cell-APC interactions have been observed in vivo, but the functional significance of unstable, serial contacts has remained unclear. Here we used multiphoton intravital microscopy in lymph nodes and tumors to show that while NFAT nuclear import was fast (t(1/2 max)∼1 min), nuclear export was slow (t(1/2)∼20 min) in T cells. During delayed export, nuclear NFAT constituted a short-term imprint of transient TCR signals and remained transcriptionally active for the T cell tolerance gene Egr2, but not for the effector gene Ifng, which required continuous TCR triggering for expression. This provides a potential mechanistic basis for the observation that a predominance of unstable APC interactions correlates with the induction of T cell tolerance.

Indexed as

Immune ToleranceImmunologic MemoryAnimalsAntigen-Presenting CellsCell CommunicationCell DifferentiationCell MovementCell NucleusCytosolEarly Growth Response Protein 2Gene Expression RegulationHumansInterferon-gammaLymph NodesMiceMicroscopy, Fluorescence, MultiphotonEarly Growth Response Protein 2Egr2 protein, mouseInterferon-gammaNFATC Transcription FactorsReceptors, Antigen, T-Cell

Identifiers

PMID23313588
PMCPMC3582823
OpenAlexW2165784749

What OpenQuestion holds

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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.