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Updated: May 20, 2026

Development of a Direct Pulp-capping Model for the Evaluation of Pulpal Wound Healing and Reparative Dentin Formation in Mice
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Lipoxin A4 and Resolvin D1 Preserve Neural Inductive Capacity of Dental Pulp Stem Cells Cultured Under Inflammatory
Ana Paula Turrioni1, Geovana Pires da Silva1, Yan Xu2
1Department of Pediatric Dentistry and Orthodontics, School of Dentistry, Federal University of Uberlandia, Uberlandia, Minas Gerais, Brazil.
Abstract:
Human dental pulp stem cells (DPSCs) exhibit neurogenic differentiation potential; however, inflammatory conditions may impair this process. This study investigated the impact of tumor necrosis factor alpha (TNF-α) on the neurodifferentiation potential of DPSCs and the modulatory role of the pro-resolving lipid mediators lipoxin A4 (LXA4) and resolvin D1 (RvD1). DPSCs were isolated and subjected to neuronal differentiation for 21 days. Cells were treated with different concentrations of TNF-α (1, 10, 25, and 100 ng/mL) and with LXA4 or RvD1 (10 and 100 nM). After 21 days, neuronal differentiation was associated with a reduction in the stem cell marker OCT3/4 (53% in the absence of TNF-α and 48.5% in the presence of TNF-α) and increased expression of the early neuronal marker doublecortin (87% in the absence of TNF-α and 116% in the presence of TNF-α). The intermediate neuronal marker βIII-tubulin increased by 135% in the absence of TNF-α but decreased by 40% in its presence. The reduction in βIII-tubulin induced by 25 ng/mL TNF-α was partially attenuated by treatment with 100 nM RvD1 (p = 0.02) or 10 nM LXA4 (p = 0.02). These findings suggest that LXA4 and RvD1 help preserve the neural differentiation potential of DPSCs cultured under inflammatory conditions.
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