Evidence map›Paper›PMID 21795397›Full record

ArticleMolecular biology of the cell2011

An active kinase domain is required for retention of PKCθ at the T cell immunological synapse.

Natalia G Cartwright, Anuj K Kashyap, Brian C Schaefer

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Intracellular Delivery of Anti-pPKCθ (Thr538) via Protein Transduction Domain Mimics for Immunomodulation.Molecular therapy : the journal of the American Society of Gene Therapy · 2016
    Article
  5. Review
  6. Review
  7. Article
  8. The Novel PKCθ from Benchtop to Clinic.Journal of immunology research · 2015
    Review
  9. Lipid-based patterning of the immunological synapse.Biochemical Society transactions · 2014
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
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

3 authors at 1 institution in 1 country.

Natalia G CartwrightDepartment of Microbiology and Immunology and Center for Neuroscience and Regenerative Medicine, Uniformed Services University, Bethesda, MD 20814, USA.
Anuj K Kashyap
Brian C Schaefer
Uniformed Services University of the Health Sciences · US

Funding

Protein redistribution in TCR-directed NF-kB activationR01AI057481 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI SCHAEFER, BRIAN · 2006 to 2010
$1.7M
NIAID NIH HHS AI057481NIAID NIH HHS R01 AI057481
6 · The paper itself

Abstract

Protein kinase Cθ (PKCθ) is a serine/threonine kinase that plays an essential role in antigen-regulated responses of T lymphocytes. Upon antigen stimulation, PKCθ is rapidly recruited to the immunological synapse (IS), the region of contact between the T cell and antigen-presenting cell. This behavior is unique among T cell PKC isoforms. To define domains of PKCθ required for retention at the IS, we generated deletion and point mutants of PKCθ. We used quantitative imaging analysis to assess IS retention of PKCθ mutants in antigen-stimulated T cell clones. Deletion of the kinase domain or site-directed mutation of a subset of known PKCθ phosphorylation sites abrogated or significantly reduced IS retention, respectively. IS retention did not correlate with phosphorylation of specific PKCθ residues but rather with kinase function. Thus PKCθ catalytic competence is essential for stable IS retention.

Indexed as

Protein TransportAmino Acid SubstitutionAnimalsCatalytic DomainCells, CulturedGreen Fluorescent ProteinsImmunological SynapsesIsoenzymesMiceMutagenesis, Site-DirectedPhosphorylationProtein Kinase CProtein Kinase C-thetaRecombinant Fusion ProteinsSingle-Cell AnalysisGreen Fluorescent ProteinsIsoenzymesPrkcq protein, mouseProtein Kinase CProtein Kinase C-thetaRecombinant Fusion Proteins

Identifiers

PMID21795397
PMCPMC3172272
OpenAlexW2105088218

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.