Evidence map›Paper›PMID 31173178›Full record

ArticleInternational journal of molecular medicine2019

Strontium promotes osteogenic differentiation by activating autophagy via the the AMPK/mTOR signaling pathway in MC3T3‑E1 cells.

You Cheng, Lunhui Huang, Yichao Wang, Qianyu Huo, Yanhong Shao, Huijing Bao, Zhaoyang Li, Yunde Liu, Xue Li

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.1field-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

29 citing papers in PubMed, 60 citations in OpenAlex.

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  13. Brevilin A inhibits RANKL-induced osteoclast differentiation and bone resorption.In vitro cellular & developmental biology. Animal · 2023
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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

9 authors at 3 institutions in 1 country.

You ChengSchool of Medical Laboratory, Tianjin Medical University, Tianjin 300070, P.R. China.
Lunhui HuangSchool of Medical Laboratory, Tianjin Medical University, Tianjin 300070, P.R. China.
Yichao WangDepartment of Clinical Laboratory Medicine, Taizhou University Hospital, Taizhou, Zhejiang 318000, P.R. China.
Qianyu HuoSchool of Medical Laboratory, Tianjin Medical University, Tianjin 300070, P.R. China.
Yanhong ShaoSchool of Medical Laboratory, Tianjin Medical University, Tianjin 300070, P.R. China.
Huijing BaoSchool of Medical Laboratory, Tianjin Medical University, Tianjin 300070, P.R. China.
Zhaoyang LiSchool of Materials Science and Engineering, Tianjin University, Tianjin 300350, P.R. China.
Yunde LiuSchool of Medical Laboratory, Tianjin Medical University, Tianjin 300070, P.R. China.
Xue LiSchool of Medical Laboratory, Tianjin Medical University, Tianjin 300070, P.R. China.
Tianjin Medical University · CNTaizhou University · CNTianjin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Strontium (Sr) is an alkaline earth metal that exerts the dual effect of improving bone formation and suppressing bone resorption, resulting in increased bone apposition rates and bone mineral density. However, the mechanisms through which Sr exerts these beneficial effects on bone have yet to be fully elucidated. The present study aimed to reveal the underlying molecular mechanisms associated with Sr‑induced osteogenic differentiation. The effects of Sr on cell proliferation and osteogenic differentiation were analyzed by MTT assay, RT‑qPCR, western blot analysis, alkaline phosphatase (ALP) and Alizarin red staining assays. The extent of autophagy was determined by monodansylcadaverine (MDC) staining and western blot analysis of two markers of cellular autophagic activity, the steatosis‑associated protein, sequestosome‑1 (SQSTM1/p62), and the two isoforms of microtubule‑associated protein 1 light chain 3 (LC3), LC‑3‑I/II. The expression levels of AMP‑activated protein kinase (AMPK) and mammalian target of rapamycin (mTOR) were also detected by western blot analysis. Sr at a concentration of 3 mM exerted the most pronounced effect on osteogenic differentiation, without any apparent cell toxicity. At the same time, cellular autophagy was active during this process. Subsequently, autophagy was blocked by 3‑methyladenine, and the enhancement of osteogenic differentiation in response to Sr was abrogated. Additionally, the phosphorylation level of AMPK was significantly increased, whereas that of mTOR was significantly decreased, in the Sr‑treated group. Taken together, the findings of the present study demonstrate that Sr stimulates AMPK‑activated autophagy to induce the osteogenic differentiation of MC3T3‑E1 cells.

Indexed as

AMP-Activated Protein KinasesAnimalsAutophagyCell DifferentiationCell LineMiceOsteogenesisSignal TransductionStrontiumTOR Serine-Threonine KinasesAMP-Activated Protein KinasesStrontiumTOR Serine-Threonine Kinases

Identifiers

PMID31173178
PMCPMC6605659
OpenAlexW2947206185

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.