Evidence map›Paper›PMID 34179305›Full record

ReviewGenes & diseases2021

The role of dendritic cells derived osteoclasts in bone destruction diseases.

Bo Wang, Yutong Dong, Zhansong Tian, Yueqi Chen, Shiwu Dong

Open access · diamondAbstract readReview
In one paragraph

Review in Genes & diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

31 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  3. Developmental Pathways of Immature CD11cInternational journal of molecular sciences · 2026
    Review
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  18. Efferocytosis and Bone Dynamics.Current osteoporosis reports · 2024
    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

5 authors at 1 institution in 1 country.

Bo WangDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, 400038, PR China.
Yutong DongDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, 400038, PR China.
Zhansong TianDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, 400038, PR China.
Yueqi ChenDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, 400038, PR China.
Shiwu DongDepartment of Biomedical Materials Science, Third Military Medical University (Army Medical University), Chongqing, 400038, PR China.
Army Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bone is previously considered as a dominant organ involved in the processes of locomotion. However, in the past two decades, a large number of studies have suggested that the skeletal system closely coordinated with the immune system so as to result in the emerging area of 'osteoimmunology'. In the evolution of many kinds of bone destruction-related diseases, osteoclasts could differentiate from dendritic cells, which contributed to increased expression of osteoclast-related membrane receptors and relatively higher activity of bone destruction, inducing severe bone destruction under inflammatory conditions. Numerous factors could influence the interaction between osteoclasts and dendritic cells, contributing to the pathogenesis of several bone diseases in the context of inflammation, including both immunocytes and a large number of cytokines. In addition, the products of osteoclasts released from bone destruction area serve as important signals for the differentiation and activation of immature dendritic cells. Therefore, the border between the dendritic cell-related immune response and osteoclast-related bone destruction has gradually unravelled. Dendritic cells and osteoclasts cooperate with each other to mediate bone destruction and bone remodelling under inflammatory conditions. In this review, we will pay attention to the interactions between dendritic cells and osteoclasts in physiological and pathological conditions to further understand the skeletal system and identify potential new therapeutic targets for the future by summarizing their significant roles and molecular mechanisms in bone destruction.

Indexed as

Bone destruction diseasesDendritic cellsOsteoclastsOsteoimmunologyTrans-differentiation

Identifiers

PMID34179305
PMCPMC8209356
OpenAlexW3015633580

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.