Evidence map›Paper›PMID 37762132›Full record

ArticleInternational journal of molecular sciences2023

Development, Establishment, and Validation of a Model for the Mineralization of Periodontium Remodelling Cells: Cementoblasts.

Shruti Bhargava, Joachim Jankowski, Erik Merckelbach, Charlotte Elisa Roth, Rogerio Bastos Craveiro, Michael Wolf

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 74% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 2 countries.

Shruti BhargavaInstitute of Molecular Cardiovascular Research, Medical Faculty, RWTH Aachen University, 52062 Aachen, Germany.
Joachim JankowskiInstitute of Molecular Cardiovascular Research, Medical Faculty, RWTH Aachen University, 52062 Aachen, Germany.
Erik MerckelbachInstitute of Molecular Cardiovascular Research, Medical Faculty, RWTH Aachen University, 52062 Aachen, Germany.
Charlotte Elisa RothDepartment of Orthodontics, Dental Clinic, University of Aachen, Pauwelsstr. 30, 52074 Aachen, Germany.
Rogerio Bastos CraveiroDepartment of Orthodontics, Dental Clinic, University of Aachen, Pauwelsstr. 30, 52074 Aachen, Germany.ORCID 0000-0003-0768-935X
Michael WolfDepartment of Orthodontics, Dental Clinic, University of Aachen, Pauwelsstr. 30, 52074 Aachen, Germany.
RWTH Aachen University · DEMaastricht University · NL

Funding

Deutsche Forschungsgemeinschaft SFB TRR 219; C-04, S-03, M-05; Project-ID: 322900939; DFG WO 2031/3-1European Union EU-ITN-H2020 ""INTRICARE"" (722609) and ""CaReSyAn"" (764474)RWTH Aachen medical faculty OCI-11the Federal Ministry of Education and Research (MIVAKA) (LS-2-1-001),
6 · The paper itself

Abstract

Chronic kidney disease (CKD) patients undergoing dialysis are at high risk of bone fractures. CKD-induced mineral and bone disorder is extended to periodontal disease due to changes in the ionic composition of saliva in CKD patients, dysregulating mineralization, hindering regeneration and thereby promoting the progression of dental complications. Despite the importance of cementum for overall oral health, the mechanisms that regulate its development and regeneration are not well comprehended, and a lack of sufficient in vitro experimental models has hindered research progress. In this study, the impact of experimental conditions on the calcification of cementoblasts was systematically investigated, aimed at establishing a standardized and validated model for the calcification of cementoblasts. The effects of phosphate, calcium, ascorbic acid, β-glycerolphosphate, dexamethasone, and fetal calf serum on the calcification process of cementoblasts were analyzed over a wide range of concentrations and time points by investigating calcium content, cell viability, gene expression and kinase activity. Cementoblasts calcified in a concentration- and time-dependent manner with higher concentrations of supplements cause a higher degree of calcification but decreased cell viability. Phosphate and calcium have a significantly stronger effect on cementoblast calcification processes compared to osteogenic supplements: ascorbic acid, β-glycerolphosphate, and dexamethasone induce calcification over a wide range of osteogenic signalling pathways, with osteopontin being a central target of gene regulation. Conversely, treatment with ascorbic acid, β-glycerolphosphate, and dexamethasone leads to activating only selected pathways, especially promoting bone sialoprotein expression. The developed and validated cementoblast calcification protocol, incubating up to 60% confluent cementoblasts with 1.9 mmol L

Indexed as

CalcinosisDental CementumAscorbic AcidCalciumCalcium, DietaryDexamethasoneGlycerophosphatesHumansOsteogenesisPeriodontiumRenal DialysisAscorbic AcidCalciumCalcium, DietaryDexamethasoneGlycerophosphatescalcificationcementoblastcementumdiabetic kidney diseaseperiodontium

Identifiers

PMID37762132
PMCPMC10531176
OpenAlexW4386562476

What OpenQuestion holds

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LicenceCC BY
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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.