Evidence map›Paper›PMID 30456702›Full record

ArticleMolecular and cellular biochemistry2019

Sirtuin 1 inhibits TNF-α-mediated osteoclastogenesis of bone marrow-derived macrophages through both ROS generation and TRPV1 activation.

Shu Yan, Lujie Miao, Yahua Lu, Liangzhi Wang

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Review
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  11. Review
  12. SIRT1 Gene SNP rs932658 Is Associated With Medication-Related Osteonecrosis of the Jaw.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  13. Article
  14. Article
  15. The Role of CaInternational journal of molecular sciences · 2020
    Review
  16. Review
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

4 authors.

Shu YanGeneral Medical Wards, The Third Affiliated Hospital of Soochow University, No. 185, Bureau Street, Tianning District, Changzhou, 213100, Jiangsu, China.
Lujie MiaoDepartment of Gastroenterology, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China.
Yahua LuGeneral Medical Wards, The Third Affiliated Hospital of Soochow University, No. 185, Bureau Street, Tianning District, Changzhou, 213100, Jiangsu, China.
Liangzhi WangGeneral Medical Wards, The Third Affiliated Hospital of Soochow University, No. 185, Bureau Street, Tianning District, Changzhou, 213100, Jiangsu, China. liangzhiwangyx@163.com.ORCID http://orcid.org/0000-0002-1599-5085

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sirtuin 1 (SIRT1), also known as NAD-dependent deacetylase, has been reported to increase in vivo osteoclast-mediated bone resorption. However, its effects on osteoclastogenesis or bone loss in vitro have not been widely examined. Therefore, the effects and underlying mechanism of SIRT1 on osteoclast differentiation in mice in vitro were studied. During RANKL-induced osteoclastogenesis in differentiated bone marrow-derived macrophages (BMMs), SIRT1 downregulation was observed. The use of resveratrol (SIRT1 activator) and SIRT1 overexpression was found to inhibit osteoclastogenesis, which was confirmed by TRAP staining and activity loss, reduced expression of osteoclast markers and related genes, and a decrease in the number of multinuclear cells. In contrast, treatment with EX-527 (SIRT1 inhibitor) as well as SIRT1 silencing promoted osteoclastogenesis. Furthermore, the tumor necrosis factor (TNF)-α level was reduced by resveratrol treatment and SIRT1 overexpression but increased following EX-527 incubation and SIRT1 depletion. TNF-α silencing blocked the osteoclastogenesis of BMMs promoted by SIRT1 depletion. Moreover, transient receptor potential vanilloid 1 (TRPV1) channel activation and reactive oxygen species (ROS) production, which are associated with osteoclastogenesis, were impaired by TNF-α silencing. These data demonstrate that SIRT1 directly inhibits osteoclastogenesis by inhibiting ROS generation and TRPV1 channel activation under mediation of TNF-α.

Indexed as

AnimalsBone Marrow CellsBone ResorptionCells, CulturedMiceOsteoclastsReactive Oxygen SpeciesSirtuin 1TRPV Cation ChannelsTumor Necrosis Factor-alphaReactive Oxygen SpeciesSirt1 protein, mouseSirtuin 1TRPV1 protein, mouseTRPV Cation ChannelsTumor Necrosis Factor-alphaBone marrow-derived macrophagesOsteoclastogenesisReactive oxygen speciesSirtuin 1Tumor necrosis factor α

Identifiers

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Registered trials

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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.