Evidence map›Paper›PMID 31774632›Full record

ArticleStem cells translational medicine2020

Skeletal stem cell-mediated suppression on inflammatory osteoclastogenesis occurs via concerted action of cell adhesion molecules and osteoprotegerin.

Xin Li, Li Ding, Yu-Xing Wang, Zhong-Li Li, Qian Wang, Zhi-Dong Zhao, Sen Zhao, Hua Wang, Chu-Tse Wu, Ning Mao and 1 more

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 77 citations in OpenAlex.

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  14. Advances in the pathogenesis of multiple myeloma bone disease.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
    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

11 authors at 3 institutions in 1 country.

Xin LiBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Li DingBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Yu-Xing WangBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Zhong-Li LiPeople's Liberation Army General Hospital, Beijing, People's Republic of China.
Qian WangBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Zhi-Dong ZhaoBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Sen ZhaoBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Hua WangBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Chu-Tse WuBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.
Ning MaoBeijing Institute of Basic Medical Sciences, Beijing, People's Republic of China.
Heng ZhuBeijing Institute of Radiation Medicine, Beijing, People's Republic of China.ORCID 0000-0002-8408-3821
Beijing Radiation Center · CNAir Force General Hospital PLA · CNBeijing Institute of Education · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the current study, we investigated how skeletal stem cells (SSCs) modulate inflammatory osteoclast (OC) formation and bone resorption. Notably, we found that intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and osteoprotegerin (OPG) play a synergistic role in SSC-mediated suppression of inflammatory osteoclastogenesis. The effect of SSCs on inflammatory osteoclastogenesis was investigated using a lipopolysaccharide-induced mouse osteolysis model in vivo and human osteoarthritis synovial fluid (OASF) in vitro. OC formation was determined by tartrate-resistant acid phosphatase staining. Bone resorption was evaluated by microcomputerized tomography, serum C-terminal telopeptide assay, and pit formation assay. The expression of ICAM-1, VCAM-1, and OPG in SSCs and their contribution to the suppression of osteoclastogenesis were determined by flow cytometry or enzyme linked immunosorbent assay. Gene modification, neutralization antibodies, and tumor necrosis factor-α knockout mice were used to further explore the mechanism. The results demonstrated that SSCs remarkably inhibited inflammatory osteoclastogenesis in vivo and in vitro. Mechanistically, inflammatory OASF stimulated ICAM-1 and VCAM-1 expression as well as OPG secretion by SSCs. In addition, ICAM-1 and VCAM-1 recruited CD11b

Indexed as

AnimalsCell Adhesion MoleculesCell DifferentiationHumansMiceOsteogenesisOsteoprotegerinStem CellsCell Adhesion MoleculesOsteoprotegerincell adhesion moleculesinflammatory osteoclastogenesisosteoprotegerinskeletal stem cells

Identifiers

PMID31774632
PMCPMC6988769
OpenAlexW2989740027

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.