A Novel Bioactive Endodontic Sealer Containing Surface-Reaction-Type Prereacted Glass-Ionomer Filler Induces Osteoblast Differentiation.

MAP kinase S‑PRG filler calcium‑sensing receptor endodontic sealer osteoblasts

Journal

Materials (Basel, Switzerland)
ISSN: 1996-1944
Titre abrégé: Materials (Basel)
Pays: Switzerland
ID NLM: 101555929

Informations de publication

Date de publication:
09 Oct 2020
Historique:
received: 20 08 2020
revised: 05 10 2020
accepted: 06 10 2020
entrez: 14 10 2020
pubmed: 15 10 2020
medline: 15 10 2020
Statut: epublish

Résumé

Surface‑reaction‑type prereacted glass-ionomer (S‑PRG) fillers exhibit bioactive properties by the release of multiple ions. This study examined whether a novel endodontic sealer containing S‑PRG fillers (PRG+) has the capacity to induce osteoblast differentiation. Kusa‑A1 osteoblastic cells were cultured with extracts of PRG+, PRG- (an experimental sealer containing S‑PRG‑free silica fillers), AH Plus (an epoxy-resin‑based sealer), and Canals N (a zinc-oxide noneugenol sealer). Cell viability and mineralized nodule formation were determined using WST‑8 assay and Alizarin red staining, respectively. Osteoblastic-marker expression was analyzed with RT‑qPCR and immunofluorescence. Phosphorylation of extracellular signal‑regulated kinase (ERK) and p38 mitogen‑activated protein kinase (MAPK) was determined with Western blotting. Extracts of freshly mixed PRG+, PRG-, and AH Plus significantly decreased cell growth, but extracts of the set samples were not significantly cytotoxic. Set PRG+ significantly upregulated mRNAs for alkaline phosphatase and bone sialoprotein (IBSP) compared to set PRG-, and upregulation was blocked by NPS2143, a calcium‑sensing receptor antagonist. Set PRG+ significantly accelerated IBSP expression, mineralized nodule formation, and enhanced the phosphorylation of ERK and p38 compared with set PRG-. In conclusion, PRG+ induced the differentiation and mineralization of Kusa‑A1 cells via the calcium-sensing receptor-induced activation of ERK and p38 MAPK.

Identifiants

pubmed: 33050334
pii: ma13204477
doi: 10.3390/ma13204477
pmc: PMC7599720
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 17H04380 to TO, 19K24137 to KH

Références

Dent Mater J. 2010 Aug;29(4):392-7
pubmed: 20610878
Sci Rep. 2019 Dec 13;9(1):19019
pubmed: 31836731
Mol Med Rep. 2018 Mar;17(3):3448-3454
pubmed: 29257332
J Biomater Appl. 2018 Jan;32(6):765-774
pubmed: 29119879
Dent Mater. 2009 Mar;25(3):360-8
pubmed: 18849067
J Biol Chem. 1998 Jan 9;273(2):1114-20
pubmed: 9422777
J Cell Physiol. 1992 Apr;151(1):197-205
pubmed: 1373147
Am J Physiol Renal Physiol. 2001 Feb;280(2):F291-302
pubmed: 11208605
PLoS One. 2018 Mar 26;13(3):e0194467
pubmed: 29579090
Physiol Rev. 2001 Jan;81(1):239-297
pubmed: 11152759
J Clin Med. 2019 Sep 11;8(9):
pubmed: 31514356
Int J Mol Sci. 2015 Oct 19;16(10):24820-38
pubmed: 26492236
Sci Rep. 2018 Jun 15;8(1):9224
pubmed: 29907831
Exp Cell Res. 2003 Nov 1;290(2):370-80
pubmed: 14567994
J Dent. 2011 Jan;39(1):72-9
pubmed: 20969915
Bone. 2008 Jan;42(1):129-38
pubmed: 17945546
J Biol Chem. 2004 Jun 11;279(24):25455-63
pubmed: 15004029
Mol Cell Biol. 2009 Nov;29(21):5843-57
pubmed: 19737917
Br J Pharmacol. 2018 Nov;175(21):4095-4108
pubmed: 29714810
Odontology. 2019 Oct;107(4):421-436
pubmed: 30554288
Int Endod J. 2010 Mar;43(3):251-7
pubmed: 20158537
Rev Endocr Metab Disord. 2001 Jan;2(1):81-94
pubmed: 11704982
Dent Mater. 2016 Sep;32(9):1095-102
pubmed: 27417376
Horm Metab Res. 2010 Aug;42(9):627-31
pubmed: 20560105
Clin Oral Investig. 2019 Apr;23(4):1723-1731
pubmed: 30159805
Int J Dent. 2014;2014:463149
pubmed: 24578706
Dent Mater J. 2011;30(6):898-903
pubmed: 22123015
J Pharmacol Exp Ther. 2012 Dec;343(3):638-49
pubmed: 22942242
Endocrinology. 2003 May;144(5):2068-74
pubmed: 12697715
Biochim Biophys Acta. 2013 Jul;1833(7):1732-44
pubmed: 23267858
J Bone Miner Res. 2011 Dec;26(12):2935-47
pubmed: 21956637
J Biol Chem. 2008 Jan 4;283(1):175-83
pubmed: 17974568
Stem Cells. 2011 Jun;29(6):981-91
pubmed: 21563277
Dent Mater J. 2006 Sep;25(3):509-15
pubmed: 17076321

Auteurs

Nobuyuki Kawashima (N)

Department of Pulp Biology and Endodontics, Division of Oral Health Sciences, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, Japan.

Kentaro Hashimoto (K)

Department of Pulp Biology and Endodontics, Division of Oral Health Sciences, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, Japan.

Masashi Kuramoto (M)

Department of Pulp Biology and Endodontics, Division of Oral Health Sciences, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, Japan.

Alamuddin Bakhit (A)

Department of Endodontics, Faculty of Dentistry, King Abdulaziz University, Jeddah 21589, UAE.

Yasumiko Wakabayashi (Y)

Department of Pulp Biology and Endodontics, Division of Oral Health Sciences, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, Japan.

Takashi Okiji (T)

Department of Pulp Biology and Endodontics, Division of Oral Health Sciences, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, Japan.

Classifications MeSH