Evidence map›Paper›PMID 29807327›Full record

ArticleMolecular immunology2018

Notch1 primes CD4 T cells for T helper type I differentiation through its early effects on miR-29.

Karthik Chandiran, Rebecca Lawlor, Antonio Pannuti, Gabriela Gonzalez Perez, Janani Srinivasan, Todd E Golde, Lucio Miele, Barbara A Osborne, Lisa M Minter

Open access · hybridAbstract read
In one paragraph

Article in Molecular immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. The role of miR-29 family in disease.Journal of cellular biochemistry · 2021
    Review
  9. Review
  10. When Viruses Cross Developmental Pathways.Frontiers in cell and developmental biology · 2021
    Review
  11. Identification of Acute Myeloid Leukemia Bone Marrow Circulating MicroRNAs.International journal of molecular sciences · 2020
    Article
  12. Review
  13. Article
  14. Non-coding RNAs in CD8 T cell biology.Molecular immunology · 2020
    Review
  15. Article
  16. Role of MicroRNAs in Parkinson's Disease.International journal of molecular sciences · 2019
    Review
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 4 institutions in 1 country.

Karthik ChandiranGraduate Program in Molecular and Cellular Biology, University of Massachusetts Amherst, Amherst, MA, 01003, United States.
Rebecca LawlorDepartment of Veterinary and Animal Sciences, University of Massachusetts Amherst, Amherst, MA, 01003, United States.
Antonio PannutiDepartment of Genetics and Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, United States.
Gabriela Gonzalez PerezDepartment of Veterinary and Animal Sciences, University of Massachusetts Amherst, Amherst, MA, 01003, United States.
Janani SrinivasanDepartment of Veterinary and Animal Sciences, University of Massachusetts Amherst, Amherst, MA, 01003, United States; Department of Biomedical Sciences, University of Illinois, Rockford College of Medicine, Rockford, IL, 61107, United States.
Todd E GoldeDepartment of Neuroscience, Center for Translational Research in Neurodegenerative Disease, and McKnight Brain Institute, College of Medicine, University of Florida, Gainesville, FL, 32610, United States.
Lucio MieleDepartment of Genetics and Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, United States.
Barbara A OsborneGraduate Program in Molecular and Cellular Biology, University of Massachusetts Amherst, Amherst, MA, 01003, United States; Department of Veterinary and Animal Sciences, University of Massachusetts Amherst, Amherst, MA, 01003, United States.
Lisa M MinterGraduate Program in Molecular and Cellular Biology, University of Massachusetts Amherst, Amherst, MA, 01003, United States; Department of Veterinary and Animal Sciences, University of Massachusetts Amherst, Amherst, MA, 01003, United States. Electronic address: lminter@vasci.umass.edu.
University of Massachusetts Amherst · USLouisiana State University Health Sciences Center New Orleans · USUniversity of Florida · USUniversity of Illinois Chicago, Rockford campus · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI JUDD E SHELLITO · 2012 to 2026
$69.1M
Targeting y-secretase in GVHDP01CA166009 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI MIELE, LUCIO · 2013 to 2017
$4.9M
NCI NIH HHS P01 CA166009NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

The transmembrane receptor, Notch1 plays an important role during the differentiation of CD4 T cells into T helper (Th) subsets in the presence of appropriate cytokines, including differentiation into Th1 cells. MicroRNAs have also been shown to be important regulators of immune responses, including negatively regulating cytokine production by Th1 cells. The miR-29 family of microRNAs can act to inhibit tbx21 and ifng transcription, two important pro-inflammatory genes that are abundantly expressed in Th1 cells. Here we show that Notch1 may prime CD4 T cells to be responsive to Th1-polarizing cues through its early repressive effects on the miR-29 family of microRNAs. Using a combination of cell lines and primary cells, we demonstrate that Notch1 can repress miR-29a, miR-29b, and miR-29c transcription through a mechanism that is independent of NF-κB. We further show that this repression is mediated by canonical Notch signaling and requires active Mastermind like (MAML) 1, but this process is superseded by positive regulation of miR-29 in response to IFNγ at later stages of CD4 T cell activation and differentiation. Collectively, our data suggest an additional mechanism by which Notch1 signaling may fine-tune Th1 cell differentiation.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell DifferentiationInterferon-gammaMiceMice, Inbred C57BLMicroRNAsNF-kappa BNIH 3T3 CellsReceptor, Notch1Signal TransductionTh1 CellsTranscription FactorsTranscription, GeneticInterferon-gammaMicroRNAsMIRN29 microRNA, mouseNF-kappa BNotch1 protein, mouseReceptor, Notch1Transcription FactorsCanonical Notch signalingCSLDN-MAMLGamma-Secretase inhibitorGSIIFNγMicroRNA-29miR-29NF-κBNotch1

Identifiers

PMID29807327
PMCPMC6281167
OpenAlexW2803824141

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.