AI Article Synopsis

  • * Researchers found that miR-3074-3p inhibits hDPSCs' ability to differentiate into odontoblasts, but using antagomiR-3074-3p-conjugated PEI-AuNPs can promote this differentiation in lab settings.
  • * In vivo experiments on rats showed that these antagomiR-3074-3p nanoparticles enhanced the formation of restorative dentin, suggesting a potential new approach for dental repair and regeneration.

Article Abstract

The odontogenic differentiation of dental pulp stem cells (DPSCs), which is vital for tooth regeneration, was regulated by various functional molecules. In recent years, a growing body of research has shown that miRNAs play a crucial role in the odontogenic differentiation of human dental pulp stem cells (hDPSCs). However, the mechanisms by which miRNAs regulated odontogenic differentiation of hDPSCs remained unclear, and the application of miRNAs in reparative dentin formation in vivo was also rare. In this study, we first discovered that miR-3074-3p had an inhibitory effect on odontogenic differentiation of hDPSCs and antagomiR-3074-3p-conjugated PEI-AuNPs effectively promoted odontogenic differentiation of hDPSCs in vitro. AntagomiR-3074-3p-conjugated PEI-AuNPs was further applied to the rat pulp-capping model and showed the increased formation of restorative dentin. In addition, the results of lentivirus transfection in vitro suggested that FKBP9 acted as the key target of miR-3074-3p in regulating the odontogenic differentiation of hDPSCs. These findings might provide a new strategy and candidate target for dentin restoration and tooth regeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333998PMC
http://dx.doi.org/10.1177/20417314231184512DOI Listing

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