Evidence map›Paper›PMID 26571489›Full record

ArticlePloS one2015

Osteoprotegerin Induces Apoptosis of Osteoclasts and Osteoclast Precursor Cells via the Fas/Fas Ligand Pathway.

Wei Liu, Chao Xu, Hongyan Zhao, Pengpeng Xia, Ruilong Song, Jianhong Gu, Xuezhong Liu, Jianchun Bian, Yan Yuan, Zongping Liu

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 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. New Horizons: Translational Aspects of Osteomorphs.The Journal of clinical endocrinology and metabolism · 2024
    Review
  9. Article
  10. Article
  11. The Mechanism of Osteoprotegerin-Induced Osteoclast Pyroptosis In Vitro.International journal of molecular sciences · 2023
    Article
  12. Review
  13. Upregulation of osteoprotegerin inhibitsExperimental and therapeutic medicine · 2022
    Article
  14. Article
  15. Determination of Therapeutic and Safety Effects ofBioMed research international · 2022
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  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

10 authors at 2 institutions in 1 country.

Wei LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Chao XuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Hongyan ZhaoCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Pengpeng XiaCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Ruilong SongCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Jianhong GuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Xuezhong LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Jianchun BianCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Yan YuanCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Zongping LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Yangzhou University · CNJiangsu Provincial Center for Disease Control and Prevention · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoprotegerin (OPG) is known to inhibit differentiation and activation of osteoclasts (OCs) by functioning as a decoy receptor blocking interactions between RANK and RANKL. However, the exact role of OPG in the survival/apoptosis of OCs remains unclear. OPG caused increased rates of apoptosis of both OCs and osteoclast precursor cells (OPCs). The expression of Fas and activated caspase-8 was increased by both 20 ng/mL and 40 ng/mL of OPG, but was markedly decreased at 80 ng/mL. Interestingly, we noted that while levels of Fas ligand (FasL) increased with increasing doses of OPG, the soluble form of FasL in the supernatant decreased. The results of a co-immunoprecipitation assay suggested that the decrease of sFasL might be caused by the binding of OPG. This would block the inhibition of the apoptosis of OCs and OPCs. Furthermore, changes in expression levels of Bax/Bcl-2, cleaved-caspase-9, cleaved-caspased-3 and the translocation of cytochrome c, illustrated that OPG induced apoptosis of OCs and OPCs via the classic Fas/FasL apoptosis pathway, and was mediated by mitochondria. Altogether, our results demonstrate that OPG induces OCs and OPCs apoptosis partly by the Fas/FasL signaling pathway.

Indexed as

ApoptosisAnimalsCells, CulturedFas Ligand Proteinfas ReceptorMaleMiceMice, Inbred BALB COsteoblastsOsteoclastsOsteoprotegerinSignal TransductionSolubilityFas Ligand ProteinFas protein, mousefas ReceptorOsteoprotegerinTnfrsf11b protein, mouse

Identifiers

PMID26571489
PMCPMC4646684
OpenAlexW2176472933

What OpenQuestion holds

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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.