Poly(Aspartic Acid) Promotes Odontoblast-like Cell Differentiation in Rat Molars with Exposed Pulp

• Published in: Journal of functional biomaterials Vol. 14; no. 11; p. 537
• Main Authors: dos Santos, Fernanda Furuse Ventura, Habelitz, Stefan, Nascimento, Fábio Dupart, Arana-Chavez, Victor Elias, Braga, Roberto Ruggiero
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01-11-2023
• Subjects: Acids; Animal models; Animals; Aspartate; Aspartic acid; calcium silicate; Capping; Cell differentiation; Cement; Collagen; Composite materials; Contamination; dental pulp capping; Dentin; dentin regeneration; Dentinogenesis; Differentiation (biology); Dmp1 protein; Ethylenediaminetetraacetic acid; Inflammation; Kinases; Mineralization; Molars; Osteopontin; Peptides; Performance evaluation; Pollution control; Proteins; Regeneration; Stem cells; Teeth; tooth remineralization; Brazil; United States > US
• ISSN: 2079-4983; 2079-4983
• DOI: 10.3390/jfb14110537

In recent years, alternative pulpal therapies targeting dentinogenesis signaling pathways using different peptides have been investigated. The aim of this study was to verify the effectiveness of poly(aspartic acid), pAsp, in dentin regeneration using an animal model. Methods: Mechanical pulp exposure was performed in the upper molars of 56 Wistar rats, randomly divided as follows (n = 14): control (no treatment); MTA group—pulp capping with mineral trioxide aggregate (MTA Angelus); pAsp group—application of 20 μL of pAsp solution (25 mg·mL−1); MTA+pAsp group—application of MTA mixed with pAsp (5:1 by mass). Animals were euthanized after 7 or 21 days. Histological sections were submitted to hematoxylin-eosin and Brown and Brenn staining and immunohistochemical analysis for osteopontin (OPN) and dentin matrix protein 1 (DMP 1). Results: At 7 days, an acute inflammatory infiltrate and the presence of disorganized mineralized tissue were observed in all groups. At 21 days, the quality and thickness of the reparative dentin in treated groups were superior to the control, and bacterial contamination was observed in two MTA-pAsp specimens. While all treated groups showed intense immunostaining for OPN at 21 days, only the pAsp group expressed DMP 1, indicating the presence of fully differentiated odontoblast-like cells. Conclusion: Poly(aspartic) acid promoted dentin regeneration in rat molars in the absence of an additional calcium source and may be an alternative to MTA as a pulp-capping agent.