Evidence map›Paper›PMID 28124096›Full record

ArticleCellular and molecular life sciences : CMLS2017

Defective germinal center B-cell response and reduced arthritic pathology in microRNA-29a-deficient mice.

Annemarie van Nieuwenhuijze, James Dooley, Stéphanie Humblet-Baron, Jayasree Sreenivasan, Marije Koenders, Susan M Schlenner, Michelle Linterman, Adrian Liston

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. IL-23 orchestrating immune cell activation in arthritis.Rheumatology (Oxford, England) · 2021
    Article
  11. Article
  12. The Role of miRNA in the Pathophysiology of Neuroendocrine Tumors.International journal of molecular sciences · 2021
    Review
  13. The role of miR-29 family in disease.Journal of cellular biochemistry · 2021
    Review
  14. Review
  15. Review
  16. Article
  17. A20: a master regulator of arthritis.Arthritis research & therapy · 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

8 authors at 4 institutions in 4 countries.

Annemarie van NieuwenhuijzeVIB Center for Brain and Disease Research, VIB, KU Leuven Campus Gasthuisberg, Herestraat 49, bus 1026, 3000, Leuven, Belgium.
James DooleyVIB Center for Brain and Disease Research, VIB, KU Leuven Campus Gasthuisberg, Herestraat 49, bus 1026, 3000, Leuven, Belgium.
Stéphanie Humblet-BaronVIB Center for Brain and Disease Research, VIB, KU Leuven Campus Gasthuisberg, Herestraat 49, bus 1026, 3000, Leuven, Belgium.
Jayasree SreenivasanVIB Center for Brain and Disease Research, VIB, KU Leuven Campus Gasthuisberg, Herestraat 49, bus 1026, 3000, Leuven, Belgium.
Marije KoendersExperimental Rheumatology, Radboud University Medical Center, 6525, Nijmegen, GA, The Netherlands.
Susan M SchlennerVIB Center for Brain and Disease Research, VIB, KU Leuven Campus Gasthuisberg, Herestraat 49, bus 1026, 3000, Leuven, Belgium.
Michelle LintermanLaboratory of Lymphocyte Signaling and Development, Babraham Institute, Cambridge, CB22 3AT, UK.
Adrian ListonVIB Center for Brain and Disease Research, VIB, KU Leuven Campus Gasthuisberg, Herestraat 49, bus 1026, 3000, Leuven, Belgium. adrian.liston@vib.be.
KU Leuven · BEBabraham Institute · GBRadboud University Nijmegen · NLVIB-KU Leuven Center for Brain & Disease Research · BE

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/000C0409
6 · The paper itself

Abstract

MicroRNA (miR) are short non-coding RNA sequences of 19-24 nucleotides that regulate gene expression by binding to mRNA target sequences. The miR-29 family of miR (miR-29a, b-1, b-2 and c) is a key player in T-cell differentiation and effector function, with deficiency causing thymic involution and a more inflammatory T-cell profile. However, the relative roles of different miR-29 family members in these processes have not been dissected. We studied the immunological role of the individual members of the miR-29 family using mice deficient for miR-29a/b-1 or miR-29b-2/c in homeostasis and during collagen-induced arthritis. We found a definitive hierarchy of immunological function, with the strong phenotype of miR-29a-deficiency in thymic involution and T-cell activation being reduced or absent in miR-29c-deficient mice. Strikingly, despite elevating the Th1 and Th17 responses, loss of miR-29a conferred near-complete protection from collagen-induced arthritis (CIA), with profound defects in B-cell proliferation and antibody production. Our results identify the hierarchical structure of the miR-29 family in T-cell biology, and identify miR-29a in B cells as a potential therapeutic target in arthritis.

Indexed as

AnimalsArthritis, ExperimentalAutoimmune DiseasesB-LymphocytesDendritic CellsGerminal CenterLymphocyte ActivationLymphocyte SubsetsMiceMice, KnockoutMicroRNAsPoly I-CThymus GlandMicroRNAsMIRN29 microRNA, mousePoly I-CAutoimmune pathologyExperimental arthritisMicroRNAThymic involution

Identifiers

PMID28124096
PMCPMC11107729
OpenAlexW2581400021

What OpenQuestion holds

Textmetadata
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.