Evidence map›Paper›PMID 18802088›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Distinct regulation of integrin-dependent T cell conjugate formation and NF-kappa B activation by the adapter protein ADAP.

Brandon J Burbach, Rupa Srivastava, Ricardo B Medeiros, William E O'Gorman, Erik J Peterson, Yoji Shimizu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  7. Measurement of T Cell Alloreactivity Using Imaging Flow Cytometry.Journal of visualized experiments : JoVE · 2017
    Article
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  9. Quantification of CD4(+) T Cell Alloreactivity and Its Control by Regulatory T Cells Using Time-Lapse Microscopy and Immune Synapse Detection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Article
  10. Review
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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.

Brandon J BurbachDepartment of Laboratory Medicine and Pathology, Masonic Cancer Center, University of Minnesota Medical School, Minneapolis, MN 55455, USA.
Rupa Srivastava
Ricardo B Medeiros
William E O'Gorman
Erik J Peterson
Yoji Shimizu
University of Minnesota Medical Center · US

Funding

MINNESOTA PAIN RESEARCH TRAINING PROGRAMT32DE007288 · NIDCR · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HERZBERG, MARK C · 1996 to 2011
$8.8M
STRUCTURE/FUNCTION ANALYSIS OF T CELL BETA1 INTEGRINR01AI038474 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SHIMIZU, YOJI · 1995 to 2014
$4.7M
Very Late Antigen Integrin Activity on T CellsR01AI031126 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SHIMIZU, YOJI · 1996 to 2010
$3.7M
The Role of ADAP in Thymic DevelopmentR01AI056016 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI PETERSON, ERIK JON · 2003 to 2007
$1.3M
NIAID NIH HHS R01 AI031126NIAID NIH HHS R01AI031126NIAID NIH HHS R01 AI038474NIAID NIH HHS R01AI038474NIAID NIH HHS R01 AI056016NIAID NIH HHS R01AI056016NIDCR NIH HHS T32 DE007288NIDCR NIH HHS T32DE007288
6 · The paper itself

Abstract

Following TCR stimulation, T cells utilize the hematopoietic specific adhesion and degranulation-promoting adapter protein (ADAP) to control both integrin adhesive function and NF-kappaB transcription factor activation. We have investigated the molecular basis by which ADAP controls these events in primary murine ADAP(-/-) T cells. Naive DO11.10/ADAP(-/-) T cells show impaired adhesion to OVAp (OVA aa 323-339)-bearing APCs that is restored following reconstitution with wild-type ADAP. Mutational analysis demonstrates that the central proline-rich domain and the C-terminal domain of ADAP are required for rescue of T:APC conjugate formation. The ADAP proline-rich domain is sufficient to bind and stabilize the expression of SKAP55 (Src kinase-associated phosphoprotein of 55 kDa), which is otherwise absent from ADAP(-/-) T cells. Interestingly, forced expression of SKAP55 in the absence of ADAP is insufficient to drive T:APC conjugate formation, demonstrating that both ADAP and SKAP55 are required for optimal LFA-1 function. Additionally, the ADAP proline-rich domain is required for optimal Ag-induced activation of CD69, CD25, and Bcl-x(L), but is not required for assembly of the CARMA1/Bcl10/Malt1 (caspase-recruitment domain (CARD) membrane-associated guanylate kinase (MAGUK) protein 1/B-cell CLL-lymphoma 10/mucosa-associated lymphoid tissue lymphoma translocation protein 1) signaling complex and subsequent TCR-dependent NF-kappaB activity. Our results indicate that ADAP is used downstream of TCR engagement to delineate two distinct molecular programs in which the ADAP/SKAP55 module is required for control of T:APC conjugate formation and functions independently of ADAP/CARMA1-mediated NF-kappaB activation.

Indexed as

Antigen PresentationAdaptor Proteins, Signal TransducingAdenoviridaeAnimalsAntigen-Presenting CellsCell AdhesionCells, CulturedHumansIntegrinsJurkat CellsLymphocyte ActivationMembrane ProteinsMiceMice, Inbred BALB CMice, KnockoutMice, TransgenicAdaptor Proteins, Signal Transducingadenovirus receptorFyb protein, mouseIntegrinsMembrane ProteinsNF-kappa BOVA 323-339OvalbuminPeptide FragmentsPhosphoproteinsReceptors, VirusSKAP1 protein, mouse

Identifiers

PMID18802088
PMCPMC2593878
OpenAlexW1957196088

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.