Evidence map›Paper›PMID 29442285›Full record

ArticleHuman cell2018

Diverse effect of BMP-2 homodimer on mesenchymal progenitors of different origin.

Edit Hrubi, László Imre, Agnieszka Robaszkiewicz, László Virág, Farkas Kerényi, Krisztina Nagy, Gábor Varga, Attila Jenei, Csaba Hegedüs

Open access · hybridAbstract read
In one paragraph

Article in Human cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Anatomical implant region - a critical determinant for the osteogenic potency of small extracellular vesicles and rhBMP-2.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2025
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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 2 countries.

Edit HrubiFaculty of Dentistry, University of Debrecen, Nagyerdei krt. 98, Debrecen, 4012, Hungary. hrubi.edit@dental.unideb.hu.
László ImreDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, Egyetem tér 1, Debrecen, 4032, Hungary.
Agnieszka RobaszkiewiczDepartment of General Biophysics, Institute of Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236, Lodz, Poland.
László VirágDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Egyetem tér 1, Debrecen, 4032, Hungary.
Farkas KerényiFaculty of Dentistry, University of Debrecen, Nagyerdei krt. 98, Debrecen, 4012, Hungary.
Krisztina NagyDepartment of Oral Biology, Semmelweis University, Nagyvárad tér 4, Budapest, 1089, Hungary.
Gábor VargaDepartment of Oral Biology, Semmelweis University, Nagyvárad tér 4, Budapest, 1089, Hungary.
Attila JeneiDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, Egyetem tér 1, Debrecen, 4032, Hungary.
Csaba HegedüsFaculty of Dentistry, University of Debrecen, Nagyerdei krt. 98, Debrecen, 4012, Hungary.
University of Debrecen · HUSemmelweis University · HUUniversity of Łódź · PL

Funding

TÁMOP 4.2.2.A-11/1/KONV-2012-0036TÁMOP TÁMOP 4.2.4.A/2-11-1-2012-0001
6 · The paper itself

Abstract

Bone morphogenetic protein-2 (BMP-2), is a potential factor to enhance osseointegration of dental implants. However, the appropriate cellular system to investigate the osteogenic effect of BMP-2 in vitro in a standardized manner still needs to be defined. The aim of this study was to examine the effect of BMP-2 on the cell proliferation and osteogenic differentiation of human osteogenic progenitors of various origins: dental pulp stem cells (DPSC), human osteosarcoma cell line (Saos-2) and human embryonic palatal mesenchymal cell line (HEPM). For induction of osteogenic differentiation, cell culture medium was supplemented with BMP-2 homodimer alone or in combination with conventionally used differentiation inducing agents. Differentiation was monitored for 6-18 days. To assess differentiation, proliferation rate, alkaline phosphatase activity, calcium deposition and the expression level of osteogenic differentiation marker genes (Runx2, BMP-2) were measured. BMP-2 inhibited cell proliferation in a concentration and time-dependent manner. In a concentration which caused maximal cell proliferation, BMP-2 did not induce osteogenic differentiation in any of the tested systems. However, it had a synergistic effect with the osteoinductive medium in both DPSC and Saos-2, but not in HEPM cells. We also found that the differentiation process was faster in Saos-2 than in DPSCs. Osteogenic differentiation could not be induced in the osteoblast progenitor HEPM cells. Our data suggest that in a concentration that inhibits proliferation the differentiation inducing effect of BMP-2 is evident only in the presence of permissive osteoinductive components. β-glycerophosphate, was identified interacting with BMP-2 in a synergistic manner.

Indexed as

Alkaline PhosphataseBone Morphogenetic Protein 2CalciumCell ProliferationCells, CulturedDental Implantation, EndosseousDental PulpDrug SynergismGlycerophosphatesHumansMesenchymal Stem CellsOsseointegrationOsteogenesisOsteosarcomaPalateProtein MultimerizationAlkaline Phosphatasebeta-glycerophosphoric acidBMP2 protein, humanBone Morphogenetic Protein 2CalciumGlycerophosphatesAlizarin redAlkaline phosphataseGrowth factorOsteogenic differentiationStem cells

Identifiers

PMID29442285
PMCPMC5852203
OpenAlexW2788096570

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.