Evidence map›Paper›PMID 31025509›Full record

ArticleJournal of cellular and molecular medicine2019

EPC-derived exosomes promote osteoclastogenesis through LncRNA-MALAT1.

Yigong Cui, Shenglong Fu, Dong Sun, Junchao Xing, Tianyong Hou, Xuehui Wu

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 4 pooled it
5.0field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 4 syntheses or guidelines pooled it, 111 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Consequences of Aging on Bone.Aging and disease · 2023
    Pooled it
  4. Pooled it
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Effects of exosomes from different origins on osteoclasts.Journal of orthopaedic surgery and research · 2025
    Review
  11. Review
  12. Exosomes promise better bone regeneration.Regenerative therapy · 2025
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Long non-coding RNAeLife · 2024
    Article
  18. Article
  19. Review
  20. Article

13 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

6 authors at 2 institutions in 1 country.

Yigong CuiDepartment of Orthopaedics, Southwest Hospital, The Third Military Medical University, Chongqing, P.R. China.
Shenglong FuDepartment of Orthopaedics, Jinan Fifth People's Hospital, Shandong, P.R. China.
Dong SunDepartment of Orthopaedics, Southwest Hospital, The Third Military Medical University, Chongqing, P.R. China.
Junchao XingDepartment of Orthopaedics, Southwest Hospital, The Third Military Medical University, Chongqing, P.R. China.
Tianyong HouDepartment of Orthopaedics, Southwest Hospital, The Third Military Medical University, Chongqing, P.R. China.
Xuehui WuDepartment of Orthopaedics, Southwest Hospital, The Third Military Medical University, Chongqing, P.R. China.ORCID 0000-0002-0961-8400
Army Medical University · CNJinan City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone repair involves bone resorption through osteoclastogenesis and the stimulation of neovascularization and osteogenesis by endothelial progenitor cells (EPCs). However, the role of EPCs in osteoclastogenesis is unclear. In this study, we assess the effects of EPC-derived exosomes on the migration and osteoclastic differentiation of primary mouse bone marrow-derived macrophages (BMMs) in vitro using immunofluorescence, western blotting, RT-PCR and Transwell assays. We also evaluated the effects of EPC-derived exosomes on the homing and osteoclastic differentiation of transplanted BMMs in a mouse bone fracture model in vivo. We found that EPCs cultured with BMMs secreted exosomes into the medium and, compared with EPCs, exosomes had a higher expression level of LncRNA-MALAT1. We confirmed that LncRNA-MALAT1 directly binds to miR-124 to negatively control miR-124 activity. Moreover, overexpression of miR-124 could reverse the migration and osteoclastic differentiation of BMMs induced by EPC-derived exosomes. A dual-luciferase reporter assay indicated that the integrin ITGB1 is the target of miR-124. Mice treated with EPC-derived exosome-BMM co-transplantations exhibited increased neovascularization at the fracture site and enhanced fracture healing compared with those treated with BMMs alone. Overall, our results suggest that EPC-derived exosomes can promote bone repair by enhancing recruitment and differentiation of osteoclast precursors through LncRNA-MALAT1.

Indexed as

AnimalsCell MovementEndothelial Progenitor CellsExosomesFracture HealingHEK293 CellsHumansIntegrin beta1MacrophagesMaleMiceMice, Inbred C57BLMicroRNAsNeovascularization, PathologicNeovascularization, PhysiologicOsteoclastsIntegrin beta1MALAT1 long non-coding RNA, humanMalat1 long non-coding RNA, mouseMicroRNAsMIRN124 microRNA, humanRNA, Long Noncodingbone marrow-derived macrophagesbone repairendothelial progenitor cellsITGB1LncRNA-MALAT1miR-124osteoclastogenesis

Identifiers

PMID31025509
PMCPMC6533478
OpenAlexW2940651922

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.