Evidence map›Paper›PMID 32488049›Full record

ArticleCell death & disease2020

Dendritic cells-derived interferon-λ1 ameliorated inflammatory bone destruction through inhibiting osteoclastogenesis.

Yueqi Chen, Yiran Wang, Ruohui Tang, Jing Yang, Ce Dou, Yutong Dong, Dong Sun, Chengmin Zhang, Lincheng Zhang, Yong Tang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Review
  3. Interferon-JAK-STAT Axis in Bone Metabolism.Current osteoporosis reports · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Role and Regulation of Transcription Factors in Osteoclastogenesis.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Multi-functional osteoclasts in matrix-based tissue engineering bone.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2022
    Review
  17. Review
  18. Review
  19. 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

14 authors at 1 institution in 1 country.

Yueqi ChenDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Yiran WangDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Ruohui TangDepartment of Emergency, Daping Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.ORCID http://orcid.org/0000-0001-6580-3259
Jing YangDepartment of Emergency, Daping Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Ce DouDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.ORCID http://orcid.org/0000-0002-6983-6354
Yutong DongDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Dong SunDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Chengmin ZhangDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Lincheng ZhangDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Yong TangDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Qijie DaiDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Fei LuoDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China.
Jianzhong XuDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China. xjzslw@163.com.
Shiwu DongDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), 400038, Chongqing, China. dongshiwu@tmmu.edu.cn.ORCID http://orcid.org/0000-0002-5032-4893
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone infection contributing to inflammatory osteolysis is common in orthopedic surgery. The dynamic balance between bone formation and bone resorption is destroyed due to excessive osteoclast fusion and differentiation, which results in severe bone matrix loss. Many therapeutic approaches that restrain osteoclast formation and function act as efficient ways to prevent inflammatory bone erosion. We have demonstrated for the first time that dendritic cells-derived interferon-λ1 (IFN-λ1) inhibited inflammatory bone destruction in vivo and explored its underlying mechanisms on osteoclast formation in vitro. We found that IFN-λ1 was highly expressed in infectious bone tissue compared with that of non-infectious bone tissue. Additionally, dendritic cells marker genes such as CD80, CD86, and CD1a were higher expressed in infectious bone tissue than that of non-infectious bone tissue. Dendritic cells that were pretreated with LPS showed high expression of IFN-λ1. Moreover, conditioned medium of LPS-pretreated dendritic cells significantly inhibited osteoclast differentiation, as determined by TRAP staining assay. This suppressive effect was reversed by adding an IFN-λ1 monoclonal antibody. It was also investigated whether exogenous IFN-λ1 restrained osteoclastogenesis, bone resorption, F-actin ring formation, osteoclast-specific gene expression, release of pro-inflammatory cytokines, and translocation of p65 and NFATc1 by preventing the NF-κB signaling pathway and NLRP3 inflammasome formation, as well as by inducing the JAK-STAT signaling pathways in vitro. In vivo study indicated that IFN-λ1 prevents lipopolysaccharide (LPS)-induced inflammatory bone destruction by inhibiting excessive osteoclast fusion and bone resorption activity. In conclusion, our findings confirmed that dendritic cells-derived IFN-λ1 could attenuate osteoclast formation and bone resorptive activity in vitro and in vivo. These novel findings pave the way for the use of exogenous IFN-λ1 as a potential therapeutic treatment for excessive osteoclast-related diseases, such as inflammatory osteolysis, by regulating osteoclastogenesis to maintain the dynamic balance between bone formation and bone resorption.

Indexed as

OsteogenesisAnimalsBone and BonesBone ResorptionCell DeathCell DifferentiationCell FusionCell NucleusCytokinesDendritic CellsGene Expression RegulationHumansInflammasomesInflammationInflammation MediatorsInterferon LambdaCytokinesInflammasomesInflammation MediatorsInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsLipopolysaccharidesNFATC Transcription FactorsNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinRANK Ligand

Identifiers

PMID32488049
PMCPMC7265503
OpenAlexW3032542573

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.