Evidence map›Paper›PMID 34865619›Full record

ArticleMolecular medicine (Cambridge, Mass.)2021

Microfibrillar-associated protein 5 regulates osteogenic differentiation by modulating the Wnt/β-catenin and AMPK signaling pathways.

Haoran Li, Wuling Zhou, Shiwei Sun, Tianlong Zhang, Tieqi Zhang, Haitian Huang, Minghai Wang

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2021. 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
2.3field-weighted citation impact, top 11% 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, 26 citations in OpenAlex.

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  10. The role of SWI/SNF complexes in digestive system neoplasms.Medical oncology (Northwood, London, England) · 2024
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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

7 authors at 1 institution in 1 country.

Haoran Li *Department of Orthopedics, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.
Wuling Zhou *Department of Orthopedics, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.
Shiwei SunDepartment of Orthopedics, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.
Tianlong ZhangDepartment of Orthopedics, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.
Tieqi ZhangDepartment of Orthopedics, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.
Haitian HuangDepartment of Orthopedics, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China.
Minghai WangDepartment of Orthopedics, Shanghai Fifth People's Hospital, Fudan University, Shanghai, China. wangminghai@5thhospital.com.ORCID 0000-0002-7940-0896
Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDysfunctional osteogenesis of bone marrow mesenchymal stem cells (BMSCs) plays an important role in osteoporosis occurrence and development. However, the molecular mechanisms of osteogenic differentiation remain unclear. This study explored whether microfibrillar-associated protein 5 (MFAP5) regulated BMSCs osteogenic differentiation.

methodsWe used shRNA or cDNA to knock down or overexpress MFAP5 in C3H10 and MC3T3-E1 cells. AR-S- and ALP-staining were performed to quantify cellular osteogenic differentiation. The mRNA levels of the classical osteogenic differentiation biomarkers Runx2, Col1α1, and OCN were quantified by qRT-PCR. Finally, we employed Western blotting to measure the levels of Wnt/β-catenin and AMPK signaling proteins.

resultsAt days 0, 3, 7, and 14 after osteogenic induction, AR-S- and ALP-staining was lighter in MFAP5 knockdown compared to control cells, as were the levels of Runx2, Col1α1 and OCN. During osteogenesis, the levels of β-catenin, p-GSK-3β, AMPK, and p-AMPK were upregulated, while that of GSK-3β was downregulated, indicating that Wnt/β-catenin and AMPK signaling were activated. The relevant molecules were expressed at lower levels in the knockdown than control group; the opposite was seen for overexpressing cell lines.

conclusionsMFAP5 regulates osteogenesis via Wnt/β‑catenin- and AMPK-signaling; MFAP5 may serve as a therapeutic target in patients with osteoporosis.

Indexed as

AMP-Activated Protein KinasesAnimalsbeta CateninCell LineContractile ProteinsFemaleGene ExpressionHumansIntercellular Signaling Peptides and ProteinsMiceOsteogenesisOsteoporosisSignal TransductionWnt ProteinsAMP-Activated Protein Kinasesbeta CateninContractile ProteinsCTNNB1 protein, humanIntercellular Signaling Peptides and ProteinsMFAP5 protein, humanWnt ProteinsAMPKBone marrow mesenchymal stem cells (BMSCs)MFAP5OsteogenesisOsteoporosisWnt/β-catenin

Identifiers

PMID34865619
PMCPMC8647299
OpenAlexW4200356306

What OpenQuestion holds

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LicenceCC BY
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.