Evidence map›Paper›PMID 33305809›Full record

ArticleThe Biochemical journal2021

Extracellular signal-regulated kinase (ERK) pathway control of CD8+ T cell differentiation.

Marcos P Damasio, Julia M Marchingo, Laura Spinelli, Jens L Hukelmann, Doreen A Cantrell, Andrew J M Howden

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
  2. SPRED2 Negatively Regulates CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. DUSP4 promotes anti-tumor CD8Nature communications · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. CCL5Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  8. Article
  9. Zeaxanthin augments CD8Cell reports. Medicine · 2025
    Article
  10. Article
  11. Clustered macrophages cooperate to eliminate tumors via coordinated intrudopodia.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Natural killer cell granule protein 7 contributes to CD8Research and practice in thrombosis and haemostasis · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Marcos P DamasioDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, DD1 5EH Dundee, U.K.
Julia M MarchingoDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, DD1 5EH Dundee, U.K.
Laura SpinelliDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, DD1 5EH Dundee, U.K.
Jens L HukelmannCentre for Gene Regulation and Expression, School of Life Sciences, University of Dundee, DD1 5EH Dundee, U.K.
Doreen A CantrellDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, DD1 5EH Dundee, U.K.
Andrew J M HowdenDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, DD1 5EH Dundee, U.K.
University of Dundee · GB

Funding

Wellcome Trust 105024/Z/14/ZWellcome Trust 202950/Z/16/ZWellcome Trust 205023/Z/16/Z
6 · The paper itself

Abstract

The integration of multiple signalling pathways that co-ordinate T cell metabolism and transcriptional reprogramming is required to drive T cell differentiation and proliferation. One key T cell signalling module is mediated by extracellular signal-regulated kinases (ERKs) which are activated in response to antigen receptor engagement. The activity of ERKs is often used to report antigen receptor occupancy but the full details of how ERKs control T cell activation is not understood. Accordingly, we have used mass spectrometry to explore how ERK signalling pathways control antigen receptor driven proteome restructuring in CD8+ T cells to gain insights about the biological processes controlled by ERKs in primary lymphocytes. Quantitative analysis of >8000 proteins identified 900 ERK regulated proteins in activated CD8+ T cells. The data identify both positive and negative regulatory roles for ERKs during T cell activation and reveal that ERK signalling primarily controls the repertoire of transcription factors, cytokines and cytokine receptors expressed by activated T cells. It was striking that a large proportion of the proteome restructuring that is driven by triggering of the T cell antigen receptor is not dependent on ERK activation. However, the selective targets of the ERK signalling module include the critical effector molecules and the cytokines that allow T cell communication with other immune cells to mediate adaptive immune responses.

Indexed as

AnimalsApoptosisBenzamidesCD8-Positive T-LymphocytesCell CycleCell ProliferationCell SurvivalChromatography, LiquidCytokinesDNA ReplicationExtracellular Signal-Regulated MAP KinasesFemaleGene OntologyLymphopoiesisMaleMAP Kinase Signaling System2-(2-chloro-4-iodophenylamino)-N-cyclopropylmethoxy-3,4-difluorobenzamideBenzamidesCytokinesExtracellular Signal-Regulated MAP KinasesProtein Kinase InhibitorsProteomeTranscription Factorsextracellular signal-regulated kinasesproteomicsT-cells

Identifiers

PMID33305809
PMCPMC7813476
OpenAlexW3111423794

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.