Evidence map›Paper›PMID 33371439›Full record

ArticleInternational journal of molecular sciences2020

TGFβ1 Suppressed Matrix Mineralization of Osteoblasts Differentiation by Regulating SMURF1-C/EBPβ-DKK1 Axis.

Bora Nam, Hyosun Park, Young Lim Lee, Younseo Oh, Jinsung Park, So Yeon Kim, Subin Weon, Sung Hoon Choi, Jae-Hyuk Yang, Sungsin Jo and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 41 citations in OpenAlex.

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  13. Oxidative medicine and cellular longevity · 2023
    Article
  14. Article
  15. Article
  16. NEDD4 E3 Ligases: Functions and Mechanisms in Bone and Tooth.International journal of molecular sciences · 2022
    Review
  17. Article
  18. Article
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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

11 authors at 3 institutions in 1 country.

Bora NamInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.
Hyosun ParkInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.ORCID 0000-0002-9737-4089
Young Lim LeeInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.
Younseo OhInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.
Jinsung ParkInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.
So Yeon KimInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.
Subin WeonInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.
Sung Hoon ChoiDepartment of Orthopedic Surgery, Hanyang University Seoul Hospital, Seoul 04763, Korea.
Jae-Hyuk YangDepartment of Orthopedic Surgery, Hanyang University Guri Hospital, Guri 11923, Korea.
Sungsin JoInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.ORCID 0000-0003-3034-5029
Tae-Hwan KimInstitute for Rheumatology Research, Hanyang University, Seoul 04763, Korea.ORCID 0000-0002-3542-2276
Hanyang University · KRHanyang University Seoul Hospital · KRHanyang University Guri Hospital · KR

Funding

Korea Health Industry Development Institute HI17C0888National Research Foundation of Korea 2019R1A2C2004214National Research Foundation of Korea 2020R1A2C1102386
6 · The paper itself

Abstract

Transforming growth factor β1 (TGFβ1) is a major mediator in the modulation of osteoblast differentiation. However, the underlying molecular mechanism is still not fully understood. Here, we show that TGFβ1 has a dual stage-dependent role in osteoblast differentiation; TGFβ1 induced matrix maturation but inhibited matrix mineralization. We discovered the underlying mechanism of the TGFβ1 inhibitory role in mineralization using human osteoprogenitors. In particular, the matrix mineralization-related genes of osteoblasts such as osteocalcin (OCN), Dickkopf 1 (DKK1), and CCAAT/enhancer-binding protein beta (C/EBPβ) were dramatically suppressed by TGFβ1 treatment. The suppressive effects of TGFβ1 were reversed with anti-TGFβ1 treatment. Mechanically, TGFβ1 decreased protein levels of C/EBPβ without changing mRNA levels and reduced both mRNA and protein levels of DKK1. The degradation of the C/EBPβ protein by TGFβ1 was dependent on the ubiquitin-proteasome pathway. TGFβ1 degraded the C/EBPβ protein by inducing the expression of the E3 ubiquitin ligase Smad ubiquitin regulatory factor 1 (SMURF1) at the transcript level, thereby reducing the C/EBPβ-DKK1 regulatory mechanism. Collectively, our findings suggest that TGFβ1 suppressed the matrix mineralization of osteoblast differentiation by regulating the SMURF1-C/EBPβ-DKK1 axis.

Indexed as

Cell DifferentiationAgedCalcification, PhysiologicCCAAT-Enhancer-Binding Protein-betaExtracellular MatrixGene Expression RegulationHumansIntercellular Signaling Peptides and ProteinsOsteoblastsOsteogenesisTransforming Growth Factor beta1Ubiquitin-Protein LigasesCCAAT-Enhancer-Binding Protein-betaCEBPB protein, humanDKK1 protein, humanIntercellular Signaling Peptides and ProteinsSMURF1 protein, humanTGFB1 protein, humanTransforming Growth Factor beta1Ubiquitin-Protein LigasesC/EBPβDKK1mineralizationosteoblast differentiationSMURF1TGFβ1

Identifiers

PMID33371439
PMCPMC7767413
OpenAlexW3118165722

What Socratic holds

Textmetadata
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 Socratic graph.