Evidence map›Paper›PMID 38418561›Full record

ArticleNPJ systems biology and applications2024

Integrative temporal multi-omics reveals uncoupling of transcriptome and proteome during human T cell activation.

Harshi Weerakoon, Ahmed Mohamed, Yide Wong, Jinjin Chen, Bhagya Senadheera, Oscar Haigh, Thomas S Watkins, Stephen Kazakoff, Pamela Mukhopadhyay, Jason Mulvenna and 3 more

Open access · goldAbstract read
In one paragraph

Article in NPJ systems biology and applications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 14 citations in OpenAlex.

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  12. Proteogenomics Reveals Microproteins in Activated T Cells.Molecular & cellular proteomics : MCP · 2025
    Article
  13. Review
  14. 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

13 authors at 5 institutions in 2 countries.

Harshi WeerakoonQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.ORCID http://orcid.org/0000-0002-8699-133X
Ahmed MohamedQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.ORCID http://orcid.org/0000-0001-6507-5300
Yide WongQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Jinjin ChenBioinformatics Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.ORCID http://orcid.org/0000-0001-7923-5723
Bhagya SenadheeraSchool of Computing, University of Colombo, Colombo, Sri Lanka.
Oscar HaighQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Thomas S WatkinsQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Stephen KazakoffQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.ORCID http://orcid.org/0000-0001-6562-1383
Pamela MukhopadhyayQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Jason MulvennaQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
John J MilesQIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Michelle M Hill *QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Ailin Lepletier *QIMR Berghofer Medical Research Institute, Herston, QLD, Australia. a.lepletierdeoliveira@griffith.edu.au.ORCID http://orcid.org/0000-0002-1371-7313
QIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUGriffith University · AUUniversity of Colombo · LKWalter and Eliza Hall Institute of Medical Research · AU

Funding

Department of Health | National Health and Medical Research Council (NHMRC) 1131732
6 · The paper itself

Abstract

Engagement of the T cell receptor (TCR) triggers molecular reprogramming leading to the acquisition of specialized effector functions by CD4 helper and CD8 cytotoxic T cells. While transcription factors, chemokines, and cytokines are known drivers in this process, the temporal proteomic and transcriptomic changes that regulate different stages of human primary T cell activation remain to be elucidated. Here, we report an integrative temporal proteomic and transcriptomic analysis of primary human CD4 and CD8 T cells following ex vivo stimulation with anti-CD3/CD28 beads, which revealed major transcriptome-proteome uncoupling. The early activation phase in both CD4 and CD8 T cells was associated with transient downregulation of the mRNA transcripts and protein of the central glucose transport GLUT1. In the proliferation phase, CD4 and CD8 T cells became transcriptionally more divergent while their proteome became more similar. In addition to the kinetics of proteome-transcriptome correlation, this study unveils selective transcriptional and translational metabolic reprogramming governing CD4 and CD8 T cell responses to TCR stimulation. This temporal transcriptome/proteome map of human T cell activation provides a reference map exploitable for future discovery of biomarkers and candidates targeting T cell responses.

Indexed as

ProteomeTranscriptomeCD3 ComplexHumansMultiomicsProteomicsReceptors, Antigen, T-CellCD3 ComplexProteomeReceptors, Antigen, T-Cell

Identifiers

PMID38418561
PMCPMC10901835
OpenAlexW4392241808

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.