Evidence map›Paper›PMID 27726217›Full record

ArticleCell proliferation2017

Low concentrations of TNF-α promote osteogenic differentiation via activation of the ephrinB2-EphB4 signalling pathway.

Limei Wang, Jin Zhang, Cunwei Wang, Yuping Qi, Mi Du, Wenhua Liu, Chengzhe Yang, Pishan Yang

Abstract read
In one paragraph

Article in Cell proliferation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 18% 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, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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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.

Limei WangDepartment of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong, China.
Jin ZhangDepartment of Endodontics, School of Stomatology, Shandong University, Jinan, Shandong, China.
Cunwei WangDepartment of Prosthodontics, School of Stomatology, Shandong University, Jinan, Shandong, China.
Yuping QiDepartment of Stomatology, Qilu Hospital, and Institute of Stomatology, Shandong University, Jinan, Shandong, China.
Mi DuDepartment of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong, China.
Wenhua LiuDepartment of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong, China.
Chengzhe YangDepartment of Oral & Maxillofacial Surgery, Qilu Hospital, and Institute of Stomatology, Shandong University, Jinan, Shandong, China.
Pishan YangDepartment of Periodontology, School of Stomatology, Shandong University, Jinan, Shandong, China.
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLow concentrations of tumour necrosis factor-alpha (TNF-α) have been reported to promote osteogenic differentiation. In this study, a series of in vitro experiments was performed to investigate underlying molecular mechanisms involved. MATERIALS AND

methodsMC3T3-E1 murine preosteoblasts were treated with TNF-α at doses of 0, 0.1 or 1 ng/mL. The ephrinB2-EphB4 signalling pathway was activated using ephrinB2-fc, or inhibited using lentiviruses encoding siRNAs specifically targeting EphB4. Cell proliferation/survival was evaluated using the Cell Counting Kit-8 (CCK-8) assay, and expression levels of Runx2, BSP, ephrinB2 and EphB4 were determined using RT-PCR and Western blotting. ALP activity in these cells was also determined, and mineral nodule formation was evaluated with alizarin red S staining.

resultsLow concentrations of TNF-α had no influence on cell proliferation/survival. However, expression levels of Runx2, BSP, ephrinB2 and EphB4, as well as ALP activity and mineral nodule formation, were significantly enhanced in MC3T3-E1 cells treated with low concentrations of TNF-α. Moreover, activation of the ephrinB2-EphB4 signalling pathway by ephrinB2-fc enhanced TNF-α-induced osteogenic differentiation, while down-regulation of EphB4 level reversed the positive effect of TNF-α.

conclusionsLow concentrations of TNF-α promoted osteogenic differentiation via activation of the ephrinB2-EphB4 signalling pathway.

Indexed as

Alkaline PhosphataseAnimalsBlotting, WesternCell DifferentiationCell LineCell ProliferationCell SurvivalCore Binding Factor Alpha 1 SubunitEphrin-B2Integrin-Binding SialoproteinMiceOsteogenesisReal-Time Polymerase Chain ReactionReceptor, EphB4RNA InterferenceRNA, MessengerAlkaline PhosphataseCore Binding Factor Alpha 1 SubunitEphb4 protein, mouseEphrin-B2Ibsp protein, mouseIntegrin-Binding SialoproteinReceptor, EphB4RNA, MessengerRNA, Small InterferingTumor Necrosis Factor-alpha

Identifiers

PMID27726217
PMCPMC6529098
OpenAlexW2531502708

What OpenQuestion holds

Textmetadata
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.