Evidence map›Paper›PMID 27359105›Full record

ArticlePloS one2016

BST2 Mediates Osteoblast Differentiation via the BMP2 Signaling Pathway in Human Alveolar-Derived Bone Marrow Stromal Cells.

Su-Hyang Yoo, Jae Goo Kim, Beom-Su Kim, Jun Lee, Sung-Hee Pi, Hyun-Dae Lim, Hong-In Shin, Eui-Sic Cho, Hyung-Keun You

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

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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 4 institutions in 1 country.

Su-Hyang YooDepartment of Periodontology, School of Dentistry, Wonkwang University, Iksan, Korea.
Jae Goo KimFaculty of Biological Science and Institute for Biodiversity Research, College of Natural Sciences, Chonbuk National University, Jeonju, Korea.
Beom-Su KimWonkwang Bone Regeneration Research Institute, Wonkwang University, Daejeon, Korea.
Jun LeeDepartment of Oral and Maxillofacial Surgery, Daejeon Dental Hospital, Wonkwang University, Daejeon, Korea.
Sung-Hee PiDepartment of Periodontology, School of Dentistry, Wonkwang University, Iksan, Korea.
Hyun-Dae LimDepartment of Oral Medicine, School of Dentistry, Wonkwang University, Iksan, Korea.
Hong-In ShinIHBR, Department of Oral Pathology, School of Dentistry, Kyungpook National University, Daegu, South Korea.
Eui-Sic ChoCluster for Craniofacial Development and Regeneration Research, Institute of Oral Biosciences, Chonbuk National University School of Dentistry, Jeonju, Korea.
Hyung-Keun YouDepartment of Periodontology, School of Dentistry, Wonkwang University, Iksan, Korea.ORCID http://orcid.org/0000-0002-4585-0477
Wonkwang University · KRJeonbuk National University · KRCell Biotech (South Korea) · KRKyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular mechanisms controlling the differentiation of bone marrow stromal stem cells into osteoblasts remain largely unknown. In this study, we investigated whether bone marrow stromal antigen 2 (BST2) influences differentiation toward the osteoblasts lineage. BST2 mRNA expression in human alveolar-derived bone marrow stromal cells (hAD-BMSCs) increased during differentiation into osteoblasts. hAD-BMSCs differentiation into osteoblasts and the mRNA expression of the bone-specific markers alkaline phosphatase, collagen type α 1, bone sialoprotein, osteocalcin, and osterix were reduced by BST2 knockdown using siRNA. Furthermore, BST2 knockdown in hAD-BMSCs resulted in decreased RUNX2 mRNA and protein expression. We hypothesized that BST2 is involved in differentiation of into osteoblasts via the BMP2 signaling pathway. Accordingly, we evaluated the mRNA expression levels of BMP2, BMP receptors (BMPR1 and 2), and the downstream signaling molecules SMAD1, SMAD4, and p-SMAD1/5/8 in BST2 knockdown cells. BMP2 expression following the induction of differentiation was significantly lower in BST2 knockdown cells than in cells treated with a non-targeting control siRNA. Similar results were found for the knockdown of the BMP2 receptor- BMPR1A. We also identified significantly lower expression of SMAD1, SMAD4, and p-SMAD1/5/8 in the BST2 knockdown cells than control cells. Our data provide the first evidence that BST2 is involved in the osteogenic differentiation of bone marrow stromal cells via the regulation of the BMP2 signaling pathway.

Indexed as

Antigens, CDBone Marrow CellsBone Marrow Stromal Antigen 2Bone Morphogenetic Protein 2Cell DifferentiationCells, CulturedGene Expression RegulationGPI-Linked ProteinsHumansMesenchymal Stem CellsMiddle AgedOsteoblastsOsteogenesisRNA, Small InterferingSignal TransductionAntigens, CDBMP2 protein, humanBone Marrow Stromal Antigen 2Bone Morphogenetic Protein 2BST2 protein, humanGPI-Linked ProteinsRNA, Small Interfering

Identifiers

PMID27359105
PMCPMC4928849
OpenAlexW2462070684

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.