Evidence map›Paper›PMID 27481129›Full record

ArticleThe Journal of experimental medicine2016

A miR-155-Peli1-c-Rel pathway controls the generation and function of T follicular helper cells.

Wen-Hsien Liu, Seung Goo Kang, Zhe Huang, Cheng-Jang Wu, Hyun Yong Jin, Christian J Maine, Yi Liu, Jovan Shepherd, Mohsen Sabouri-Ghomi, Alicia Gonzalez-Martin and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 6% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Role of miR-155 in inflammatory autoimmune diseases: a comprehensive review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. miRNA Molecules-Late Breaking Treatment for Inflammatory Bowel Diseases?International journal of molecular sciences · 2023
    Review
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  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Vaccine-induced ICOSCell reports. Medicine · 2021
    Article
  19. Review
  20. 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

17 authors at 6 institutions in 3 countries.

Wen-Hsien LiuState Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China cxiao@scripps.edu whliu@xmu.edu.cn guofu@xmu.edu.cn.ORCID 0000-0003-2500-3892
Seung Goo KangDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037 Division of Biomedical Convergence/Institute of Bioscience and Biotechnology, College of Biomedical Science, Kangwon National University, Chuncheon 24341, Republic of Korea.
Zhe HuangDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
Cheng-Jang WuDivision of Biological Sciences, Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093.
Hyun Yong JinDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
Christian J MaineDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
Yi LiuDepartment of Microbiology, Immunology, and Molecular Genetics, Institute for Quantitative and Computational Biosciences, University of California, Los Angeles, Los Angeles, CA 90095.ORCID 0000-0003-1372-2101
Jovan ShepherdDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
Mohsen Sabouri-GhomiDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.ORCID 0000-0001-7770-5314
Alicia Gonzalez-MartinDepartment of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037.
Shunbin XuDepartment of Ophthalmology/Kresge Eye Institute, School of Medicine, Wayne State University, Detroit, MI 48202 Department of Anatomy and Cell Biology, School of Medicine, Wayne State University, Detroit, MI 48202.ORCID 0000-0002-6140-0943
Alexander HoffmannDepartment of Microbiology, Immunology, and Molecular Genetics, Institute for Quantitative and Computational Biosciences, University of California, Los Angeles, Los Angeles, CA 90095.ORCID 0000-0002-5607-3845
Ye ZhengNomis Foundation Laboratories for Immunobiology and Microbial Pathogenesis, Salk Institute for Biological Studies, La Jolla, CA 92037.ORCID 0000-0001-5012-4309
Li-Fan LuDivision of Biological Sciences, Moores Cancer Center, University of California, San Diego, La Jolla, CA 92093.ORCID 0000-0002-9727-0036
Nengming XiaoState Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China.ORCID 0000-0001-5417-707X
Guo FuState Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China cxiao@scripps.edu whliu@xmu.edu.cn guofu@xmu.edu.cn.
Changchun XiaoState Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen 361005, China Department of Immunology and Microbial Science, The Scripps Research Institute, La Jolla, CA 92037 cxiao@scripps.edu whliu@xmu.edu.cn guofu@xmu.edu.cn.ORCID 0000-0001-8754-3208
Scripps Research Institute · USXiamen University · CNQB3 · USUniversity of California San Diego · USSalk Institute for Biological Studies · USWayne State University · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
Treg development and function controlled by cis-regulatory circuitsR01AI107027 · NIAID · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI ZHENG, YE · 2014 to 2022
$5.0M
Role of microRNAs in regulatory T cell-mediated immunological tolerance and T celR01AI108651 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2014 to 2024
$4.0M
The miR-183/96/182 Cluster in Pseudomonas aeruginosa-induced KeratitisR01EY026059 · NEI · WAYNE STATE UNIVERSITY · PI SHUNBIN XU · 2017 to 2026
$3.7M
Modeling KSHV latency in vivoR01CA103646 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CESARMAN, ETHEL · 2004 to 2016
$3.5M
Regulation of T Follicular Helper Cell Differentiation by MicroRNAsR01AI121155 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 2016 to 2020
$2.8M
The Role of miR-17~92 in Autoimmune DiseasesR01AI087634 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI XIAO, CHANGCHUN · 2010 to 2014
$2.2M
Functional Analysis of MicroRNAs in Lymphocyte Development and Immune ToleranceR01AI089854 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI XIAO, CHANGCHUN · 2011 to 2014
$1.2M
Regulation of T Follicular Helper Cell Differentiation by MicroRNAsR56AI110403 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI XIAO, CHANGCHUN · 2015 to 2015
$474k
The role of SOCS1 repression by miR-155 in regulating immune responsivenessR21AI103646 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2013 to 2014
$426k
Regulation of T Follicular Helper Cell Differentiation by MicroRNAsR56AI121155 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI XIAO, CHANGCHUN · 2016 to 2016
$131k
NCI NIH HHS P30 CA014195NCI NIH HHS R01 CA103646NEI NIH HHS R01 EY026059NIAID NIH HHS R01 AI087634NIAID NIH HHS R01 AI089854NIAID NIH HHS R01 AI107027NIAID NIH HHS R01 AI108651NIAID NIH HHS R01 AI121155NIAID NIH HHS R21 AI103646NIAID NIH HHS R56 AI110403NIAID NIH HHS R56 AI121155
6 · The paper itself

Abstract

MicroRNA (miRNA) deficiency impairs the generation of T follicular helper (Tfh) cells, but the contribution of individual miRNAs to this phenotype remains poorly understood. In this study, we performed deep sequencing analysis of miRNAs expressed in Tfh cells and identified a five-miRNA signature. Analyses of mutant mice deficient of these miRNAs revealed that miR-22 and miR-183/96/182 are dispensable, but miR-155 is essential for the generation and function of Tfh cells. miR-155 deficiency led to decreased proliferation specifically at the late stage of Tfh cell differentiation and reduced CD40 ligand (CD40L) expression on antigen-specific CD4(+) T cells. Mechanistically, miR-155 repressed the expression of Peli1, a ubiquitin ligase that promotes the degradation of the NF-κB family transcription factor c-Rel, which controls cellular proliferation and CD40L expression. Therefore, our study identifies a novel miR-155-Peli1-c-Rel pathway that specifically regulates Tfh cell generation and function.

Indexed as

AnimalsCD40 LigandCell DifferentiationMiceMice, Inbred C57BLMicroRNAsNF-kappa BNuclear ProteinsProto-Oncogene Proteins c-relSignal TransductionT-Lymphocytes, CytotoxicT-Lymphocytes, Helper-InducerUbiquitin-Protein LigasesCD40 LigandMicroRNAsMirn155 microRNA, mouseMirn183 microRNA, mouseMirn96 microRNA, mouseNF-kappa BNuclear ProteinsPeli1 protein, mouseProto-Oncogene Proteins c-relUbiquitin-Protein Ligases

Identifiers

PMID27481129
PMCPMC4995083
OpenAlexW2482433771

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.