Evidence map›Paper›PMID 37759563›Full record

ReviewBiology2023

A Story of Kinases and Adaptors: The Role of Lck, ZAP-70 and LAT in Switch Panel Governing T-Cell Development and Activation.

Luis M Fernández-Aguilar, Inmaculada Vico-Barranco, Mikel M Arbulo-Echevarria, Enrique Aguado

Open access · goldAbstract readReview
In one paragraph

Review in Biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
9.5field-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

30 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Post-Translational Regulation of CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  5. CD147 regulates CD8iScience · 2026
    Article
  6. Review
  7. Association ofFrontiers in bioinformatics · 2026
    Article
  8. Post-translational modifications in CD8Frontiers in immunology · 2026
    Review
  9. Review
  10. Article
  11. Review
  12. Nanoscale restructuring of the immune synapse with an engager enhances NK cell function.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Impacts of rs7528684 (-169T/C) onFrontiers in genetics · 2025
    Article
  20. 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

4 authors at 1 institution in 1 country.

Luis M Fernández-AguilarInstitute for Biomedical Research of Cadiz (INIBICA), 11009 Cadiz, Spain.
Inmaculada Vico-BarrancoInstitute for Biomedical Research of Cadiz (INIBICA), 11009 Cadiz, Spain.ORCID 0000-0002-4279-7244
Mikel M Arbulo-EchevarriaInstitute for Biomedical Research of Cadiz (INIBICA), 11009 Cadiz, Spain.
Enrique AguadoInstitute for Biomedical Research of Cadiz (INIBICA), 11009 Cadiz, Spain.ORCID 0000-0002-7232-2661
Universidad de Cádiz · ES

Funding

Agencia Estatal de Investigación, Ministerio de Ciencia e Innovación, Spain PID2020-113943RB-I00Consejería de Transformación Económica, Industria, Conocimiento y Universidades, Junta de Andalucía, Spain PAIDI2020/DOC_01433Consejería de Transformación Económica, Industria, Conocimiento y Universidades, Junta de Andalucía, Spain PY20_01297University of Cádiz PR2022-037
6 · The paper itself

Abstract

Specific antigen recognition is one of the immune system's features that allows it to mount intense yet controlled responses to an infinity of potential threats. T cells play a relevant role in the host defense and the clearance of pathogens by means of the specific recognition of peptide antigens presented by antigen-presenting cells (APCs), and, to do so, they are equipped with a clonally distributed antigen receptor called the T-cell receptor (TCR). Upon the specific engagement of the TCR, multiple intracellular signals are triggered, which lead to the activation, proliferation and differentiation of T lymphocytes into effector cells. In addition, this signaling cascade also operates during T-cell development, allowing for the generation of cells that can be helpful in the defense against threats, as well as preventing the generation of autoreactive cells. Early TCR signals include phosphorylation events in which the tyrosine kinases Lck and ZAP70 are involved. The sequential activation of these kinases leads to the phosphorylation of the transmembrane adaptor LAT, which constitutes a signaling hub for the generation of a signalosome, finally resulting in T-cell activation. These early signals play a relevant role in triggering the development, activation, proliferation and apoptosis of T cells, and the negative regulation of these signals is key to avoid aberrant processes that could generate inappropriate cellular responses and disease. In this review, we will examine and discuss the roles of the tyrosine kinases Lck and ZAP70 and the membrane adaptor LAT in these cellular processes.

Indexed as

CD3ITAMsLATLcksignalingTCRZAP70

Identifiers

PMID37759563
PMCPMC10525366
OpenAlexW4386121328

What OpenQuestion holds

Textmetadata
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.