Evidence map›Paper›PMID 35916930›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2022

Human mast cells induce osteoclastogenesis through cell surface RANKL.

Chun Wai Ng, Ben Chung Lap Chan, Chun Hay Ko, Issan Yee San Tam, Sze Wing Sam, Clara Bik San Lau, Ping Chung Leung, Hang Yung Alaster Lau

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  10. Article
  11. Role of Mast-Cell-Derived RANKL in Ovariectomy-Induced Bone Loss in Mice.International journal of molecular sciences · 2023
    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

8 authors at 1 institution in 1 country.

Chun Wai NgSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Ben Chung Lap ChanInstitute of Chinese Medicine and State Key Laboratory of Research On Bioactivities and Clinical Applications of Medicinal Plants, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Chun Hay KoInstitute of Chinese Medicine and State Key Laboratory of Research On Bioactivities and Clinical Applications of Medicinal Plants, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Issan Yee San TamSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Sze Wing SamSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Clara Bik San LauInstitute of Chinese Medicine and State Key Laboratory of Research On Bioactivities and Clinical Applications of Medicinal Plants, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Ping Chung LeungInstitute of Chinese Medicine and State Key Laboratory of Research On Bioactivities and Clinical Applications of Medicinal Plants, The Chinese University of Hong Kong, Hong Kong, SAR, China.
Hang Yung Alaster LauSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong, SAR, China. hyalau@cuhk.edu.hk.
Chinese University of Hong Kong · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe employed the co-culture of CD34

methodsMature HMC and osteoclast precursors were cultured from monocytes isolated from human buffy coat. The osteoclast precursors were incubated with HMC or receptor activator of nuclear factor kappa-B ligand (RANKL) for a week prior to determination of osteoclast maturation through characterization by their morphology and tartrate resistant acid phosphatase (TRAP) expression. The bone absorption activity was determined by pit formation on osteo-assay plate.

resultsMature osteoclasts were identified following co-culture of osteoclast precursors with HMC for one week in the absence of RANKL and they were capable of bone resorption. These actions of HMC on osteoclasts were not affected by mast cell activators such anti-IgE or substance P but could be reversed by osteoprotegerin (OPG) in the co-culture system suggesting the involvement of RANKL. The expression of RANKL on the cell surface of HMC was confirmed by flow cytometry and the density was not affected by activation of HMC.

conclusionOur study provided direct evidence confirming the initiation of osteoclast proliferation and activation by mast cells through cell surface RANKL suggesting that mast cells may contribute to bone destruction in pathological conditions such as osteoporosis.

Indexed as

Mast CellsOsteoporosisCell DifferentiationCells, CulturedHumansMembrane GlycoproteinsNF-kappa BOsteoclastsOsteogenesisOsteoprotegerinRANK LigandReceptor Activator of Nuclear Factor-kappa BMembrane GlycoproteinsNF-kappa BOsteoprotegerinRANK LigandReceptor Activator of Nuclear Factor-kappa BTNFSF11 protein, humanMast cellOsteoclastOsteoclastogenesisOsteoporosisRANKL

Identifiers

PMID35916930
OpenAlexW4289522243

What OpenQuestion holds

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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.