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Development of a Direct Pulp-capping Model for the Evaluation of Pulpal Wound Healing and Reparative Dentin Formation in Mice
Published on: January 12, 2017
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microRNA-200c Mitigates Pulpitis and Promotes Dentin Regeneration.
Tadkamol Krongbaramee1,2, Chawin Upara1, Matthew T Remy1
1Iowa Institute for Oral Health Research, College of Dentistry, the University of Iowa, Iowa City, IA 52242, USA.
International Journal of Molecular Sciences
|July 29, 2025
Summary
MicroRNA-200c (miR-200c) is downregulated in inflamed dental pulp. Overexpressing miR-200c reduces inflammation and promotes dentin regeneration, showing promise for vital pulp therapy.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Oral Biology
Background:
- MicroRNA (miR)-200c plays a role in osteogenesis and dentin development.
- Inflammation and impaired dentin regeneration are key challenges in vital pulp therapy (VPT).
Purpose of the Study:
- To investigate the potential of miR-200c in mitigating pulpitis and promoting dentin regeneration for improved VPT outcomes.
- To explore miR-200c expression in inflamed pulp tissues and dental pulp cells (DPCs).
Main Methods:
- Assessed miR-200c expression in human inflamed pulp tissues and Porphyromonas gingivalis lipopolysaccharide (Pg-LPS)-challenged DPCs.
- Overexpressed miR-200c using plasmid DNA (pDNA) in vitro and evaluated its effects on odontogenic differentiation and inflammation.
- Utilized CaCO3-based nanoparticles to deliver pDNA encoding miR-200c in a rat pulpitis model.
Main Results:
- Downregulation of miR-200c was observed in inflamed pulp tissues and DPCs.
- miR-200c overexpression reduced pro-inflammatory cytokines (IL-6, IL-8) in DPCs.
- Enhanced expression of odontogenic markers (Runx2, OCN, DMP1, DSPP) and promoted dentin formation in vivo.
Conclusions:
- Locally applied miR-200c effectively modulates pulpal inflammation.
- miR-200c promotes dentin repair, indicating its therapeutic potential for vital pulp therapy.
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