Evidence map›Paper›PMID 21788445›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

MicroRNA regulation of molecular networks mapped by global microRNA, mRNA, and protein expression in activated T lymphocytes.

Yevgeniy A Grigoryev, Sunil M Kurian, Traver Hart, Aleksey A Nakorchevsky, Caifu Chen, Daniel Campbell, Steven R Head, John R Yates, Daniel R Salomon

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

54 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
  2. Article
  3. MicroRNAs: The Missing Link between Hypertension and Periodontitis?International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. A holistic miRNA-mRNA module discovery.Non-coding RNA research · 2021
    Article
  10. Article
  11. Dynamic chromatin regulatory landscape of human CAR T cell exhaustion.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Article
  13. Article
  14. Mesenchymal stem cells negatively regulate CD4Molecular medicine reports · 2021
    Article
  15. Article
  16. Article
  17. Non-coding RNAs in CD8 T cell biology.Molecular immunology · 2020
    Review
  18. Review
  19. Review
  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

9 authors at 2 institutions in 1 country.

Yevgeniy A GrigoryevDepartment of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
Sunil M Kurian
Traver Hart
Aleksey A Nakorchevsky
Caifu Chen
Daniel Campbell
Steven R Head
John R Yates
Daniel R Salomon
Scripps Research Institute · USAnsys (United States) · US

Funding

Quantitative Biology CoreU19AI063603 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI YATES III, JOHN R · 2004 to 2015
$26.4M
MicroRNA regulation of human T and B cell activationR01AI081757 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI SALOMON, DANIEL R. · 2009 to 2013
$2.3M
NIAID NIH HHS R01 AI081757NIAID NIH HHS U19 AI063603PHS HHS U19 A1063603
6 · The paper itself

Abstract

MicroRNAs (miRNAs) regulate specific immune mechanisms, but their genome-wide regulation of T lymphocyte activation is largely unknown. We performed a multidimensional functional genomics analysis to integrate genome-wide differential mRNA, miRNA, and protein expression as a function of human T lymphocyte activation and time. We surveyed expression of 420 human miRNAs in parallel with genome-wide mRNA expression. We identified a unique signature of 71 differentially expressed miRNAs, 57 of which were previously not known as regulators of immune activation. The majority of miRNAs are upregulated, mRNA expression of these target genes is downregulated, and this is a function of binding multiple miRNAs (combinatorial targeting). Our data reveal that consideration of this complex signature, rather than single miRNAs, is necessary to construct a full picture of miRNA-mediated regulation. Molecular network mapping of miRNA targets revealed the regulation of activation-induced immune signaling. In contrast, pathways populated by genes that are not miRNA targets are enriched for metabolism and biosynthesis. Finally, we specifically validated miR-155 (known) and miR-221 (novel in T lymphocytes) using locked nucleic acid inhibitors. Inhibition of these two highly upregulated miRNAs in CD4(+) T cells was shown to increase proliferation by removing suppression of four target genes linked to proliferation and survival. Thus, multiple lines of evidence link top functional networks directly to T lymphocyte immunity, underlining the value of mapping global gene, protein, and miRNA expression.

Indexed as

Cell SeparationComputational BiologyFlow CytometryGene ExpressionGene Expression ProfilingGenomicsHumansLymphocyte ActivationMicroRNAsProteomicsReverse Transcriptase Polymerase Chain ReactionRNA, MessengerT-LymphocytesMicroRNAsRNA, Messenger

Identifiers

PMID21788445
PMCPMC3159804
OpenAlexW2139339448

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.