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High-plasticity mineral trioxide aggregate and its effects on M1 and M2 macrophage viability and adherence, phagocyte activity, production of reactive oxygen species, and cytokines

Restorative Dentistry & Endodontics 2023³â 48±Ç 1È£ p.6 ~ 6
Betania Canal Vasconcellos, Layara Cristine Tomaz Tavares, Danilo Couto da Silva, Francielen Oliveira Fonseca, Francine Benetti, Antonio Paulino Ribeiro Sobrinho, Warley Luciano Fonseca Tavares,
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 ( Betania Canal Vasconcellos ) - 
 ( Layara Cristine Tomaz Tavares ) - 
 ( Danilo Couto da Silva ) - 
 ( Francielen Oliveira Fonseca ) - 
 ( Francine Benetti ) - 
 ( Antonio Paulino Ribeiro Sobrinho ) - 
 ( Warley Luciano Fonseca Tavares ) - 

Abstract


Objectives: This study evaluated the effects of high-plasticity mineral trioxide aggregate (MTA-HP) on the activity of M1 and M2 macrophages, compared to white MTA (Angelus).

Materials and Methods: Peritoneal inflammatory M1 (from C57BL/6 mice) and M2 (from BALB/c mice) macrophages were cultured in the presence of the tested materials. Cell viability (MTT and trypan blue assays), adhesion, phagocytosis, reactive oxygen species (ROS) production, and tumor necrosis factor (TNF)-¥á and transforming growth factor (TGF)-¥â production were evaluated. Parametric analysis of variance and the non-parametric Kruskal-Wallis test were used. Results were considered significant when p < 0.05.

Results: The MTT assay revealed a significant decrease in M1 metabolism with MTA-HP at 24 hours, and with MTA and MTA-HP later. The trypan blue assay showed significantly fewer live M1 at 48 hours and live M2 at 48 and 72 hours with MTA-HP, compared to MTA. M1 and M2 adherence and phagocytosis showed no significant differences compared to control for both materials. Zymosan A stimulated ROS production by macrophages. In the absence of interferon-¥ã, TNF-¥á production by M1 did not significantly differ between groups. For M2, both materials showed higher TNF-¥á production in the presence of the stimulus, but without significant between-group differences. Likewise, TGF-¥â production by M1 and M2 macrophages was not significantly different between the groups.

Conclusions: M1 and M2 macrophages presented different viability in response to MTA and MTA-HP at different time points. Introducing a plasticizer into the MTA vehicle did not interfere with the activity of M1 and M2 macrophages.

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Cytokines; Macrophages; Mineral trioxide aggregate

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