Evidence map›Paper›PMID 27646003›Full record

ArticleThe Journal of biological chemistry2016

MicroRNA-205 Maintains T Cell Development following Stress by Regulating Forkhead Box N1 and Selected Chemokines.

Ashley R Hoover, Igor Dozmorov, Jessica MacLeod, Qiumei Du, M Teresa de la Morena, Joseph Forbess, Kristine Guleserian, Ondine B Cleaver, Nicolai S C van Oers

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Immunosenescence: signaling pathways, diseases and therapeutic targets.Signal transduction and targeted therapy · 2025
    Review
  2. Article
  3. Comprehensive phenotypic analysis of diverse FOXN1 variants.The Journal of allergy and clinical immunology · 2023
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. sncRNA-1 Is a Small Noncoding RNA Produced byFrontiers in microbiology · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Functional Role of MicroRNAs in Thymocyte Development.International archives of allergy and immunology
    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 2 institutions in 1 country.

Ashley R HooverFrom the Departments of Immunology.
Igor DozmorovFrom the Departments of Immunology.
Jessica MacLeodFrom the Departments of Immunology.
Qiumei DuFrom the Departments of Immunology.
M Teresa de la MorenaPediatrics.
Joseph ForbessInternal Medicine.
Kristine GuleserianInternal Medicine.
Ondine B CleaverMolecular Biology, and.
Nicolai S C van OersFrom the Departments of Immunology, nicolai.vanoers@utsouthwestern.edu.
Pediatrics and Genetics · USMolecular Biology Consortium · US

Funding

Long noncoding RNAs and their contribution to 22q11.2 deletion syndromeR01AI114523 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI VAN OERS, NICOLAI STANISLAS CYRILLE · 2015 to 2024
$4.1M
The lnc to clinical abnormalities in 22q11_2 deletion DiGeorge syndromeF31AI110140 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI HOOVER, ASHLEY RENAE · 2014 to 2015
$61k
NIAID NIH HHS F31 AI110140NIAID NIH HHS R01 AI114523
6 · The paper itself

Abstract

The thymus, an organ responsible for T cell development, is one of the more stress-sensitive tissues in the body. Stress, in the form of infections, radiation exposure, and steroids, impairs thymic epithelial cell (TEC) functions and induces the programmed cell death of immature thymocytes. MicroRNAs are small noncoding RNAs involved in tissue repair and homeostasis, with several supporting T cell development. We report that miR-205, an epithelial-specific miR, maintains thymopoiesis following inflammatory perturbations. Thus, the activation of diverse pattern recognition receptors in mice causes a more severe thymic hypoplasia and delayed T cell recovery when miR-205 is conditionally ablated in TECs. Gene expression comparisons in the TECs with/without miR-205 revealed a significant differential regulation of chemokine/chemokine receptor pathways, antigen processing components, and changes in the Wnt signaling system. This was partly a consequence of reduced expression of the transcriptional regulator of epithelial cell function, Forkhead Box N1 (Foxn1), and its two regulated targets, stem cell factor and ccl25, following stress. miR-205 mimics supplemented into miR-205-deficient fetal thymic organ cultures restored Foxn1 expression along with ccl25 and stem cell factor A number of putative targets of miR-205 were up-regulated in TECs lacking miR-205, consistent with an important role for this miR in supporting T cell development in response to stress.

Indexed as

Cell DifferentiationAnimalsCells, CulturedChemokines, CCFemaleForkhead Transcription FactorsMaleMiceMice, Inbred C57BLMice, KnockoutMicroRNAsStem Cell FactorThymocytesThymus GlandT-LymphocytesCcl25 protein, mouseChemokines, CCForkhead Transcription FactorsMicroRNAsMIRN205 microRNA, mouseStem Cell FactorWhn proteindevelopmentlipopolysaccharide (LPS)microRNA (miRNA)pathogen-associated molecular pattern (PAMP)pattern recognition receptor (PRR)stressstress responseT-cell biology

Identifiers

PMID27646003
PMCPMC5087740
OpenAlexW2521916664

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.