Evidence map›Paper›PMID 30443989›Full record

ArticleCell proliferation2019

AP2a enhanced the osteogenic differentiation of mesenchymal stem cells by inhibiting the formation of YAP/RUNX2 complex and BARX1 transcription.

Xiao Lin, Haoqing Yang, Lijun Wang, Wenzhi Li, Shu Diao, Juan Du, Songlin Wang, Rui Dong, Jun Li, Zhipeng Fan

Open access · hybridAbstract read
In one paragraph

Article in Cell proliferation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  15. Cell-based therapies for rheumatoid arthritis: opportunities and challenges.Therapeutic advances in musculoskeletal disease · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. An overview of signaling pathways regulating YAP/TAZ activity.Cellular and molecular life sciences : CMLS · 2021
    Review
  20. 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

10 authors at 1 institution in 1 country.

Xiao LinLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Haoqing YangLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Lijun WangLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Wenzhi LiLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Shu DiaoLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Juan DuLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Songlin WangMolecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Rui DongLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.
Jun LiDepartment of Implant Dentistry, Capital Medical University School of Stomatology, Beijing, China.
Zhipeng FanLaboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory for Tooth Regeneration and Function Reconstruction of Oral Tissues, Capital Medical University School of Stomatology, Beijing, China.ORCID http://orcid.org/0000-0003-0629-3476
Capital Medical University · CN

Funding

National Natural Science Foundation of China 81570936 81625005
6 · The paper itself

Abstract

objectivesBone regeneration by bone tissue engineering is a therapeutic option for bone defects. Improving the osteogenic differentiation of mesenchymal stem cells (MSCs) is essential for successful bone regeneration. We previously showed that AP2a enhances the osteogenic differentiation in MSCs. The present study investigated the mechanism of how AP2a regulates the direct differentiation. MATERIALS AND

methodsCo-immunoprecipitation and ChIP assays were carried out to investigate the underlying mechanism in MSCs differentiation. The osteogenic differentiation potential was determined by mineralization ability and the expression of osteogenic marker in vitro and the in vivo bone-like tissue generation in nude mice.

resultsWe show that AP2a can compete with RUNX2, a key transcription factor in osteogenic differentiation, to recruit YAP and release the inhibition of RUNX2 activity from YAP by forming YAP-AP2a protein complex. YAP-AP2a protein complex also interacts with the BARX1 promoter through AP2a, inhibit the transcription of BARX1. Moreover, BARX1 inhibits osteogenic differentiation of MSCs.

conclusionsOur discoveries revealed that AP2a may regulate the osteogenic differentiation in an indirect way through competing with RUNX2 to relieve the RUNX2 activity which inhibited by YAP, and also in a direct way via targeting the BARX1 and directly repressed its transcription. Thus, our discoveries shed new light on the mechanism of direct differentiation of MSCs and provide candidate targets for improving the osteogenic differentiation and enhancing bone tissue regeneration.

Indexed as

Adaptor Protein Complex 2Adaptor Protein Complex alpha SubunitsAnimalsBone RegenerationCalcium PhosphatesCell Cycle ProteinsCell LineCore Binding Factor Alpha 1 SubunitDurapatiteFemaleGene Expression RegulationHEK293 CellsHomeodomain ProteinsHumansMesenchymal Stem CellsMiceAdaptor Protein Complex 2Adaptor Protein Complex alpha SubunitsAP2A1 protein, humanBARX1 protein, humanCalcium PhosphatesCell Cycle ProteinsCore Binding Factor Alpha 1 SubunitDurapatiteHomeodomain ProteinsNuclear ProteinsRNA, Small InterferingRUNX2 protein, humanTranscription Factorstricalcium phosphateYY1AP1 protein, humanAP2aBARX1mesenchymal stem cellsosteogenic differentiationyes-associated protein

Identifiers

PMID30443989
PMCPMC6430486
OpenAlexW2901011352

What OpenQuestion 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 OpenQuestion graph.