Evidence map›Paper›PMID 26908631›Full record

ArticleJournal of dental research2016

Characterization of Regulatory Extracellular Vesicles from Osteoclasts.

N Huynh, L VonMoss, D Smith, I Rahman, M F Felemban, J Zuo, W J Rody, K P McHugh, L S Holliday

Open access · greenAbstract read
In one paragraph

Article in Journal of dental research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

126 citing papers in PubMed, 187 citations in OpenAlex.

  1. Trial
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  8. Article
  9. MicroRNAs in neurodegenerative diseases: from molecular mechanisms to clinical biomarkers, detection methods and therapeutic strategies-advances and challenges.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Review
  10. Article
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  14. Isolation of Extracellular Vesicle Subtypes from Primary Osteoblast Cultures.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  15. Effect of primary osteoblast-derived extracellular vesicles on osteoclast differentiation.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2024
    Article
  16. Article
  17. Advances in the Study of Extracellular Vesicles for Bone Regeneration.International journal of molecular sciences · 2024
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  18. Review
  19. Review
  20. Natural medicine delivery from 3D printed bone substitutes.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review

66 more citing papers are in PubMed but not listed here.

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.

N HuynhDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
L VonMossDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
D SmithDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
I RahmanDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
M F FelembanDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
J ZuoDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
W J RodyDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
K P McHughDepartment of Periodontics, University of Florida College of Dentistry, Gainesville, FL, USA.
L S HollidayDepartment of Orthodontics, University of Florida College of Dentistry, Gainesville, FL, USA Department of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL, USA sholliday@dental.ufl.edu.
Florida College · USUniversity of Florida · US

Funding

Dental applications for a novel osteoclast inhibitorR21DE019862 · NIDCR · UNIVERSITY OF FLORIDA · PI HOLLIDAY, LEXIE SHANNON · 2010 to 2011
$401k
NIDCR NIH HHS R21 DE019862
6 · The paper itself

Abstract

Extracellular vesicles (EVs), which include exosomes and ectosomes/microvesicles, have emerged as important intercellular regulators. EVs can interact with surface receptors of target cells and can transport luminal components, including messenger RNAs (mRNAs), microRNAs, and enzymes, to the cytosol of the target cell. Here, we show that hematopoietic cells grown in culture shed exosome-like EVs as they differentiate from preosteoclasts into osteoclasts. These EVs were between 25 and 120 nm (mean, 40 nm) in diameter determined by transmission electron microscopy. The exosome-associated markers CD63 and EpCAM were enriched in the isolated EVs while markers of Golgi and endoplasmic reticulum were not detected. Treatment of isolated hematopoietic cells with EVs did not affect their receptor activator of nuclear factor κB-ligand (RANKL)-stimulated differentiation into osteoclasts. However, EVs from osteoclast precursors promoted 1,25-dihydroxyvitamin D3-dependent osteoclast formation in whole mouse marrow cultures, and EVs from osteoclast-enriched cultures inhibited osteoclastogenesis in the same cultures. These data suggested that osteoclast-derived EVs are paracrine regulators of osteoclastogenesis. EVs from mature osteoclasts contained receptor activator of nuclear factor κB (RANK). Immunogold labeling showed RANK was enriched in 1 in every 32 EVs isolated from osteoclast-enriched cultures. Depletion of RANK-rich EVs relieved the ability of osteoclast-derived EVs to inhibit osteoclast formation in 1,25-dihydroxyvitamin D3-stimulated marrow cultures. In summary, we show for the first time that EVs released by osteoclasts are novel regulators of osteoclastogenesis. Our data suggest that RANK in EVs may be mechanistically linked to the inhibition of osteoclast formation. RANK present in EVs may function by competitively inhibiting the stimulation of RANK on osteoclast surfaces by RANKL similar to osteoprotegerin. RANK-rich EVs may also take advantage of the RANK/RANKL interaction to target RANK-rich EVs to RANKL-bearing cells for the delivery of other regulatory molecules.

Indexed as

AnimalsBiomarkersBone Marrow CellsCalcitriolCell CommunicationCell DifferentiationCells, CulturedCell SurvivalExtracellular VesiclesMiceMicroscopy, Electron, TransmissionOsteoclastsRANK LigandReceptor Activator of Nuclear Factor-kappa BBiomarkersCalcitriolRANK LigandReceptor Activator of Nuclear Factor-kappa Bboneexosomemicrovesicleosteoblastosteoprotegerinreceptor activator of nuclear factor kappa B ligand

Identifiers

PMID26908631
PMCPMC4924543
OpenAlexW2274581845

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.