Blood Clotting Dissolution in the Presence of a Magnetic Field and Preliminary Study with MG63 Osteoblast-like Cells-Further Developments for Guided Bone Regeneration?

MG63 osteoblast-like cells clot stability fibrinolysis guided bone regeneration static magnetic field tissue-type plasminogen activator trypsin

Journal

Bioengineering (Basel, Switzerland)
ISSN: 2306-5354
Titre abrégé: Bioengineering (Basel)
Pays: Switzerland
ID NLM: 101676056

Informations de publication

Date de publication:
26 Jul 2023
Historique:
received: 26 05 2023
revised: 21 07 2023
accepted: 24 07 2023
medline: 26 8 2023
pubmed: 26 8 2023
entrez: 26 8 2023
Statut: epublish

Résumé

The influence of a magnetic field on the activation of bone cells and remodelling of alveolar bone is known to incite bone regeneration. Guided Bone Regeneration (GBR) aims to develop biomimetic scaffolds to allow for the functioning of the barrier and the precise succession of wound healing steps, including haemostasis. The effect of a magnetic field on blood clot dissolution has not been studied yet. We conducted a methodological study on the clot stability in the presence of a static magnetic field (SMF). Preformed whole blood (WB) clots were treated with either a broad proteolytic enzyme (trypsin) or a specific fibrinolytic agent, i.e., tissue-type plasminogen activator (t-PA). MG63 osteoblast-like cells were added to preformed WB clots to assess cell proliferation. After having experienced a number of clotting and dissolution protocols, we obtained clot stability exerted by SMF when tissue factor (for clotting) and t-PA + plasminogen (for fibrinolysis) were used. WB clots allowed osteoblast-like cells to survive and proliferate, however no obvious effects of the magnetic field were noted. Paramagnetic properties of erythrocytes may have influenced the reduction in clot dissolution. Future studies are warranted to fully exploit the combination of magnetic forces, WB clot and cells in GBR applied to orthodontics and prosthodontics.

Sections du résumé

BACKGROUND BACKGROUND
The influence of a magnetic field on the activation of bone cells and remodelling of alveolar bone is known to incite bone regeneration. Guided Bone Regeneration (GBR) aims to develop biomimetic scaffolds to allow for the functioning of the barrier and the precise succession of wound healing steps, including haemostasis. The effect of a magnetic field on blood clot dissolution has not been studied yet.
METHODS METHODS
We conducted a methodological study on the clot stability in the presence of a static magnetic field (SMF). Preformed whole blood (WB) clots were treated with either a broad proteolytic enzyme (trypsin) or a specific fibrinolytic agent, i.e., tissue-type plasminogen activator (t-PA). MG63 osteoblast-like cells were added to preformed WB clots to assess cell proliferation.
RESULTS RESULTS
After having experienced a number of clotting and dissolution protocols, we obtained clot stability exerted by SMF when tissue factor (for clotting) and t-PA + plasminogen (for fibrinolysis) were used. WB clots allowed osteoblast-like cells to survive and proliferate, however no obvious effects of the magnetic field were noted.
CONCLUSIONS CONCLUSIONS
Paramagnetic properties of erythrocytes may have influenced the reduction in clot dissolution. Future studies are warranted to fully exploit the combination of magnetic forces, WB clot and cells in GBR applied to orthodontics and prosthodontics.

Identifiants

pubmed: 37627773
pii: bioengineering10080888
doi: 10.3390/bioengineering10080888
pmc: PMC10451701
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Osteophenix Italia
ID : N/A

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Auteurs

Sante Di Gioia (S)

Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.

Lucio Milillo (L)

Independent Researcher, 70126 Bari, Italy.

Md Niamat Hossain (MN)

Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.

Annalucia Carbone (A)

Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.

Massimo Petruzzi (M)

Department of Interdisciplinary Medicine, University of Bari "Aldo Moro", 70126 Bari, Italy.

Massimo Conese (M)

Department of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.

Classifications MeSH