Evidence map›Paper›PMID 25923429›Full record

ArticlePloS one2015

Free Extracellular miRNA Functionally Targets Cells by Transfecting Exosomes from Their Companion Cells.

Krzysztof Bryniarski, Wlodzimierz Ptak, Emilia Martin, Katarzyna Nazimek, Marian Szczepanik, Marek Sanak, Philip W Askenase

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

44 citing papers in PubMed, 76 citations in OpenAlex.

  1. Review
  2. mTOR Signaling in Macrophages: All Depends on the Context.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Macrophage Functions in Psoriasis: Lessons from Mouse Models.International journal of molecular sciences · 2024
    Review
  5. Review
  6. Article
  7. Extracellular Vesicles-Oral Therapeutics of the Future.International journal of molecular sciences · 2022
    Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Intestinal effect of the probioticJournal of diabetes and metabolic disorders · 2020
    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

7 authors at 2 institutions in 2 countries.

Krzysztof BryniarskiSection of Allergy and Clinical Immunology, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America; Department of Immunology, Jagiellonian University Medical College, Krakow, Poland.
Wlodzimierz PtakDepartment of Immunology, Jagiellonian University Medical College, Krakow, Poland.
Emilia MartinDepartment of Immunology, Jagiellonian University Medical College, Krakow, Poland.
Katarzyna NazimekDepartment of Immunology, Jagiellonian University Medical College, Krakow, Poland.
Marian SzczepanikDepartment of Medical Biology, Jagiellonian University Medical College, Krakow, Poland.
Marek SanakDepartment of Internal Medicine, Jagiellonian University Medical College, Krakow, Poland.
Philip W AskenaseSection of Allergy and Clinical Immunology, Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Jagiellonian University · PLYale University · US

Funding

SOC CoreU54DA036134 · NIDA · BAYLOR COLLEGE OF MEDICINE · PI GALAS, DAVID J., GERSTEIN, MARK BENDER · 2013 to 2018
$15.0M
ALLERGY AND IMMUNOLOGY TRAINING GRANTT32AI007174 · NIAID · YALE UNIVERSITY · PI ASKENASE, PHILIP WILLIAM · 1985 to 2015
$2.6M
The Role of AID in Contact SensitivityR21AI076366 · NIAID · YALE UNIVERSITY · PI ASKENASE, PHILIP WILLIAM · 2009 to 2010
$636k
NIAID NIH HHS AI-05981NIAID NIH HHS AI-07174NIAID NIH HHS AI-076366NIAID NIH HHS R21 AI076366NIAID NIH HHS T32 AI007174NIDA NIH HHS U54 DA036134
6 · The paper itself

Abstract

Lymph node and spleen cells of mice doubly immunized by epicutaneous and intravenous hapten application produce a suppressive component that inhibits the action of the effector T cells that mediate contact sensitivity reactions. We recently re-investigated this phenomenon in an immunological system. CD8+ T lymphocyte-derived exosomes transferred suppressive miR-150 to the effector T cells antigen-specifically due to exosome surface coat of antibody light chains made by B1a lymphocytes. Extracellular RNA (exRNA) is protected from plasma RNases by carriage in exosomes or by chaperones. Exosome transfer of functional RNA to target cells is well described, whereas the mechanism of transfer of exRNA free of exosomes remains unclear. In the current study we describe extracellular miR-150, extracted from exosomes, yet still able to mediate antigen-specific suppression. We have determined that this was due to miR-150 association with antibody-coated exosomes produced by B1a cell companions of the effector T cells, which resulted in antigen-specific suppression of their function. Thus functional cell targeting by free exRNA can proceed by transfecting companion cell exosomes that then transfer RNA cargo to the acceptor cells. This contrasts with the classical view on release of RNA-containing exosomes from the multivesicular bodies for subsequent intercellular targeting. This new alternate pathway for transfer of exRNA between cells has distinct biological and immunological significance, and since most human blood exRNA is not in exosomes may be relevant to evaluation and treatment of diseases.

Indexed as

AnimalsAntibodiesCD8-Positive T-LymphocytesCell LineExosomesHumansLymphocyte ActivationMice, Inbred C57BLMicroRNAsToll-Like Receptor 3TransfectionAntibodiesMicroRNAsMirn150 microRNA, mouseTLR3 protein, mouseToll-Like Receptor 3

Identifiers

PMID25923429
PMCPMC4414541
OpenAlexW2027723253

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.