Heparin is biocompatible and can induce differentiation of human dental pulp cells.

bone morphogenetic protein-2 cytotoxicity dental pulp cells heparin osteogenic bioactivity

Journal

International endodontic journal
ISSN: 1365-2591
Titre abrégé: Int Endod J
Pays: England
ID NLM: 8004996

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 28 02 2018
accepted: 14 12 2018
pubmed: 20 12 2018
medline: 30 10 2019
entrez: 20 12 2018
Statut: ppublish

Résumé

To investigate the biocompatibility, osteogenic bioactivity and mRNA expression of the osteo/odontogenic markers bone morphogenetic protein 2 (BMP-2), osteocalcin (OC) and alkaline phosphatase (ALP), induced by heparin in human dental pulp cells (hDPCs). hDPCs were exposed to the heparin, and cell viability was assessed by 3-(4,5-dimethylthiazol)-2,5-diphenyltetrazolium bromide (MTT), and cell death was evaluated by flow cytometry. Osteogenic bioactivity was evaluated by the alkaline phosphatase (ALP) assay, and the detection of calcium deposits by alizarin red staining (ARS). The gene expression of BMP-2, OC and ALP was quantified with real-time PCR. Statistical analysis was performed with ANOVA and Bonferroni or Tukey post-test and t-test (α = 0.05). Heparin had no cytotoxic effect and did not induce apoptosis. After 3 days, heparin had significantly higher ALP activity in comparison with the control (P < 0.05). Heparin had a significant (P < 0.05) stimulatory effect on the formation of mineralized nodules. BMP-2 and OC mRNA expressions were significantly higher in cells exposed to heparin than control group after 1 day (P < 0.05). Heparin was biocompatible in hDPCs, induced osteogenic bioactivity and enhanced mRNA expression of osteo/odontogenic markers BMP-2 and OC. These results suggest that heparin has potential to induce osteo/odontogenic cell differentiation of hDPCs.

Identifiants

pubmed: 30565254
doi: 10.1111/iej.13061
doi:

Substances chimiques

Heparin 9005-49-6
Alkaline Phosphatase EC 3.1.3.1

Types de publication

Journal Article

Langues

eng

Pagination

829-837

Subventions

Organisme : São Paulo Research Foundation - FAPESP
ID : 2010/15278-6, 2015/03437-6, 2011/13116-1
Organisme : CAPES
ID : 2016/1604159

Informations de copyright

© 2018 International Endodontic Journal. Published by John Wiley & Sons Ltd.

Auteurs

E M Rodrigues (EM)

Department of Restorative Dentistry, Dental School of São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.

A L G Cornélio (ALG)

Department of Restorative Dentistry, Dental School of São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.

P H Godoi (PH)

National Institute of Metrology, Quality and Technology, Rio de Janeiro, Brazil.

P I da Costa (PI)

Department of Bioscience and Biotechnology Applied to Pharmacy of São, São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.

C Rossa-Junior (C)

Department of Diagnosis and Surgery, Dental School of São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.

G Faria (G)

Department of Restorative Dentistry, Dental School of São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.

J M Guerreiro Tanomaru (JM)

Department of Restorative Dentistry, Dental School of São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.

M Tanomaru-Filho (M)

Department of Restorative Dentistry, Dental School of São Paulo State University-UNESP, Araraquara, São Paulo, Brazil.

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Classifications MeSH