Platelet-rich fibrin suppresses in vitro osteoclastogenesis.


Journal

Journal of periodontology
ISSN: 1943-3670
Titre abrégé: J Periodontol
Pays: United States
ID NLM: 8000345

Informations de publication

Date de publication:
03 2020
Historique:
received: 19 02 2019
revised: 28 06 2019
accepted: 02 07 2019
pubmed: 6 8 2019
medline: 3 7 2020
entrez: 6 8 2019
Statut: ppublish

Résumé

Platelet-rich fibrin (PRF) membranes can preserve alveolar ridge dimension after tooth extraction. Thus, it can be presumed that PRF suppresses the catabolic events that are caused by osteoclastic bone resorption. To address this possibility, we investigated the impact of soluble extracts of PRF membranes on in vitro osteoclastogenesis in murine bone marrow cultures. Osteoclastogenesis was induced by exposing murine bone marrow cultures to receptor activator of nuclear factor kappa B ligand (RANKL), macrophage colony-stimulating factor (M-CSF) and transforming growth factor-beta 1 (TGF-β1) in the presence or absence of PRF. Osteoclastogenesis was evaluated based on histochemical, gene expression, and resorption analysis. Viability was confirmed by formation of formazan crystals, live-dead staining and caspase-3 activity assay. We report here that in vitro osteoclastogenesis is greatly suppressed by soluble extracts of PRF membranes as indicated by tartrate-resistant acid phosphatase (TRAP) staining and pit formation. In support of the histochemical observations, soluble extracts of PRF membranes decreased expression levels of the osteoclast marker genes TRAP, Cathepsin K, dendritic cell-specific transmembrane protein (DCSTAMP), nuclear factor of activated T-cells (NFATc1), and osteoclast-associated receptor (OSCAR). PRF membranes, however, cannot reverse the process once osteoclastogenesis has evolved. These in vitro findings indicate that PRF membranes can inhibit the formation of osteoclasts from hematopoietic progenitors in bone marrow cultures. Overall, our results imply that the favorable effects of PRF membranes in alveolar ridge preservation may be attributed, at least in part, by the inhibition of osteoclastogenesis.

Sections du résumé

BACKGROUND
Platelet-rich fibrin (PRF) membranes can preserve alveolar ridge dimension after tooth extraction. Thus, it can be presumed that PRF suppresses the catabolic events that are caused by osteoclastic bone resorption.
METHODS
To address this possibility, we investigated the impact of soluble extracts of PRF membranes on in vitro osteoclastogenesis in murine bone marrow cultures. Osteoclastogenesis was induced by exposing murine bone marrow cultures to receptor activator of nuclear factor kappa B ligand (RANKL), macrophage colony-stimulating factor (M-CSF) and transforming growth factor-beta 1 (TGF-β1) in the presence or absence of PRF. Osteoclastogenesis was evaluated based on histochemical, gene expression, and resorption analysis. Viability was confirmed by formation of formazan crystals, live-dead staining and caspase-3 activity assay.
RESULTS
We report here that in vitro osteoclastogenesis is greatly suppressed by soluble extracts of PRF membranes as indicated by tartrate-resistant acid phosphatase (TRAP) staining and pit formation. In support of the histochemical observations, soluble extracts of PRF membranes decreased expression levels of the osteoclast marker genes TRAP, Cathepsin K, dendritic cell-specific transmembrane protein (DCSTAMP), nuclear factor of activated T-cells (NFATc1), and osteoclast-associated receptor (OSCAR). PRF membranes, however, cannot reverse the process once osteoclastogenesis has evolved.
CONCLUSION
These in vitro findings indicate that PRF membranes can inhibit the formation of osteoclasts from hematopoietic progenitors in bone marrow cultures. Overall, our results imply that the favorable effects of PRF membranes in alveolar ridge preservation may be attributed, at least in part, by the inhibition of osteoclastogenesis.

Identifiants

pubmed: 31381154
doi: 10.1002/JPER.19-0109
pmc: PMC7155126
doi:

Substances chimiques

NFATC Transcription Factors 0
RANK Ligand 0
Macrophage Colony-Stimulating Factor 81627-83-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

413-421

Subventions

Organisme : Austrian Science Fund FWF
ID : I 4072
Pays : Austria

Informations de copyright

© 2019 The Authors. Journal of Periodontology published by Wiley Periodicals, Inc. on behalf of American Academy of Periodontology.

Références

Biomed Res Int. 2014;2014:692913
pubmed: 25136613
Transfusion. 2017 Apr;57(4):1058-1065
pubmed: 28182293
J Clin Periodontol. 2016 Nov;43(11):990-999
pubmed: 27509214
J Periodontol. 2018 Apr;89(4):379-387
pubmed: 29683498
J Biol Chem. 2005 Sep 23;280(38):32905-13
pubmed: 16046394
J Periodontol. 2017 Jan;88(1):112-121
pubmed: 27587367
Platelets. 2018 Jan;29(1):48-55
pubmed: 28351189
Cell Metab. 2007 Jun;5(6):464-75
pubmed: 17550781
J Orthop Res. 2010 Jun;28(6):792-7
pubmed: 20058277
Endocr Rev. 1999 Jun;20(3):345-57
pubmed: 10368775
J Periodontol. 2019 Jan;90(1):61-71
pubmed: 29958327
J Clin Periodontol. 2005 Feb;32(2):212-8
pubmed: 15691354
Biomaterials. 2016 Jan;76:371-87
pubmed: 26561934
J Cell Sci. 2000 Jul;113 ( Pt 13):2445-53
pubmed: 10852823
FEBS Lett. 2017 Mar;591(5):728-736
pubmed: 28173622
Immunology. 2016 Nov;149(3):320-328
pubmed: 27421990
J Periodontol. 2020 Feb;91(2):244-252
pubmed: 31376159
Clin Oral Investig. 2016 Dec;20(9):2353-2360
pubmed: 26809431
Clin Implant Dent Relat Res. 2018 Feb;20(1):82-91
pubmed: 29283206
Int J Mol Sci. 2014 May 14;15(5):8509-25
pubmed: 24830554
Front Bioeng Biotechnol. 2018 Aug 14;6:104
pubmed: 30155464
J Orthop Res. 2013 Oct;31(10):1561-9
pubmed: 23703957
Bone. 2002 May;30(5):726-32
pubmed: 11996911
J Periodontol. 2020 Mar;91(3):413-421
pubmed: 31381154
Clin Oral Implants Res. 2018 Oct;29 Suppl 18:6-19
pubmed: 30306698
J Exp Med. 2004 Oct 4;200(7):941-6
pubmed: 15452179
Sci Rep. 2017 Apr 12;7:46452
pubmed: 28401929
J Periodontol. 2019 Feb;90(2):122-125
pubmed: 30548620
Int J Oral Maxillofac Implants. 2018 Nov/Dec;33(6):1206-1212
pubmed: 30427950
Tissue Eng Part B Rev. 2017 Feb;23(1):83-99
pubmed: 27672729
Endocrinology. 1988 Apr;122(4):1373-82
pubmed: 3345718

Auteurs

Zahra Kargarpour (Z)

Department of Oral Biology, Medical University of Vienna, Vienna, Austria.
Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

Jila Nasirzade (J)

Department of Oral Biology, Medical University of Vienna, Vienna, Austria.
Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

Franz Josef Strauss (FJ)

Department of Oral Biology, Medical University of Vienna, Vienna, Austria.
Department of Conservative Dentistry, School of Dentistry, University of Chile, Santiago, Chile.

Francesca Di Summa (F)

Department of Oral Biology, Medical University of Vienna, Vienna, Austria.

Sadegh Hasannia (S)

Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

Heinz-Dieter Müller (HD)

Department of Oral Biology, Medical University of Vienna, Vienna, Austria.

Reinhard Gruber (R)

Department of Oral Biology, Medical University of Vienna, Vienna, Austria.
Department of Periodontology, School of Dental Medicine, University of Bern, Bern, Switzerland.

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Classifications MeSH