Evidence map›Paper›PMID 31119382›Full record

ArticleClinical oral investigations2020

Synergistic potential of 1α,25-dihydroxyvitamin D3 and calcium-aluminate-chitosan scaffolds with dental pulp cells.

Ester Alves Ferreira Bordini, Fernanda Balestrero Cassiano, Isabela Sanches Pompeo Silva, Felipe Rochelle Usberti, Giovana Anovazzi, Leandro Edgar Pacheco, Taísa Nogueira Pansani, Maria Luísa Leite, Josimeri Hebling, Carlos Alberto de Souza Costa and 1 more

Abstract read
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In one paragraph

Article in Clinical oral investigations, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Review
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  8. Article
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  10. Article
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  12. Article
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  14. Nanoparticles in Dentistry: A Comprehensive Review.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Application of Chitosan in Bone and Dental Engineering.Molecules (Basel, Switzerland) · 2019
    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

11 authors.

Ester Alves Ferreira BordiniDepartment of Physiology and Pathology, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Humaita Street, 1680, Araraquara, SP, 14801-903, Brazil.
Fernanda Balestrero CassianoDepartment of Physiology and Pathology, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Humaita Street, 1680, Araraquara, SP, 14801-903, Brazil.
Isabela Sanches Pompeo SilvaDepartment of Operative Dentistry, Endodontics and Dental Materials, Bauru School of Dentistry-FOB, Sao Paulo University - USP, Al. Dr. Octavio Pinheiro Brizola, 9-75, Bauru, SP, 17012-901, Brazil.
Felipe Rochelle UsbertiDepartment of Physiology and Pathology, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Humaita Street, 1680, Araraquara, SP, 14801-903, Brazil.
Giovana AnovazziDepartment of Orthodontics and Pediatric Dentistry, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Araraquara, SP, Brazil. Humaitá Street, 1680, Araraquara, SP, 14801-903, Brazil.
Leandro Edgar PachecoDepartment of Operative Dentistry, Endodontics and Dental Materials, Bauru School of Dentistry-FOB, Sao Paulo University - USP, Al. Dr. Octavio Pinheiro Brizola, 9-75, Bauru, SP, 17012-901, Brazil.
Taísa Nogueira PansaniDepartment of Physiology and Pathology, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Humaita Street, 1680, Araraquara, SP, 14801-903, Brazil.
Maria Luísa LeiteDepartment of Physiology and Pathology, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Humaita Street, 1680, Araraquara, SP, 14801-903, Brazil.
Josimeri HeblingDepartment of Orthodontics and Pediatric Dentistry, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Araraquara, SP, Brazil. Humaitá Street, 1680, Araraquara, SP, 14801-903, Brazil.
Carlos Alberto de Souza CostaDepartment of Physiology and Pathology, Araraquara School of Dentistry, Univ. Estadual Paulista - UNESP, Humaita Street, 1680, Araraquara, SP, 14801-903, Brazil.
Diana Gabriela SoaresDepartment of Operative Dentistry, Endodontics and Dental Materials, Bauru School of Dentistry-FOB, Sao Paulo University - USP, Al. Dr. Octavio Pinheiro Brizola, 9-75, Bauru, SP, 17012-901, Brazil. soares.dg@usp.br.ORCID http://orcid.org/0000-0002-1485-6104

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/15674-5Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/20181-0
6 · The paper itself

Abstract

objectivesThis study aimed to develop a porous chitosan-calcium-aluminate scaffold (CH-AlCa) in combination with a bioactive dosage of 1α,25-dihydroxyvitamin D3 (1α,25VD), to be used as a bioactive substrate capable to increase the odontogenic potential of human dental pulp cells (HDPCs). MATERIALS AND

methodsThe porous CH-AlCa was developed by the incorporation of an AlCa suspension into a CH solution under vigorous agitation, followed by phase separation at low temperature. Scaffold architecture, porosity, and calcium release were evaluated. Thereafter, the synergistic potential of CH-AlCa and 1 nM 1α,25VD, selected by a dose-response assay, for HDPCs seeded onto the materials was assessed.

resultsThe CH-AlCa featured an organized and interconnected pore network, with increased porosity in comparison with that of plain chitosan scaffolds (CH). Increased odontoblastic phenotype expression on the human dental pulp cell (HDPC)/CH and HDPC/CH-AlCa constructs in the presence of 1 nM 1α,25VD was detected, since alkaline phosphatase activity, mineralized matrix deposition, dentin sialophosphoprotein/dentin matrix acidic phosphoprotein 1 mRNA expression, and cell migration were overstimulated. This drug featured a synergistic effect with CH-AlCa, since the highest values of cell migration and odontoblastic markers expression were observed in this experimental condition.

conclusionsThe experimental CH-AlCa scaffold increases the chemotaxis and regenerative potential of HDPCs, and the addition of low-dosage 1α,25VD to this scaffold enhances the potential of these cells to express an odontoblastic phenotype. CLINICAL RELEVANCE: Chitosan scaffolds enriched with calcium-aluminate in association with low dosages of 1α,25-dihydroxyvitamin D3 provide a highly bioactive microenvironment for dental pulp cells prone to dentin regeneration, thus providing potential as a cell-free tissue engineering system for direct pulp capping.

Indexed as

Dental PulpCalciumCell DifferentiationCell ProliferationCells, CulturedChitosanHumansOdontoblastsTissue ScaffoldsCalciumChitosanDental pulpScaffoldsStem cellsTissue engineering

Identifiers

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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.