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Updated: May 5, 2026

Inducing Apical Periodontitis in Mice
Published on: August 6, 2019
MicroRNAs: new insights into the pathogenesis of endodontic periapical disease
Linda T Chan1, Sheng Zhong, Afsar Raza Naqvi
1Department of Endodontics, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina.
Introduction:
Apical periodontitis is an inflammatory disease of the periradicular tissues caused by the host's immune response to infection of the root canal system. MicroRNAs (miRNAs) have been shown to play an important role in the regulation of inflammation and the immune response; however, their role in the pathogenesis of endodontic periapical disease has not been explored. The purpose of this study was to examine the differential expression of miRNAs in diseased periapical tissues as compared with healthy controls.
Methods:
We first compared miRNA profiles in diseased periapical tissues collected from patients undergoing endodontic surgery with those of healthy pulps by using microarray analyses. The target genes of the differentially expressed miRNAs were identified by using miRWalk and PubMed. Selected miRNAs linked to inflammation and the immune response were then confirmed in a separate cohort of diseased and healthy tissues by using quantitative reverse transcription-polymerase chain reaction. Healthy pulps and periodontal ligaments were used as controls. Data were normalized to the level of SNORD 44, which served as an endogenous control.
Results:
Of the 381 miRNAs identified by using microarray, 24 miRNAs were down-regulated in diseased periapical tissues compared with controls (n = 13) (P < .003). The down-regulation of 7 miRNAs was confirmed from 9 selected miRNAs by using quantitative real-time polymerase chain reaction (n = 19) (P < .05). Target genes of these miRNAs include key mediators in the immune and inflammatory response such as interleukin-6, matrix metalloproteinase-9, and transforming growth factor-β.
Conclusions:
These findings offer new insight into the pathogenesis of endodontic disease and have the potential to impact the development of new methods for prevention, diagnosis, and treatment of apical periodontitis.
Insights
MicroRNAs (miRNAs) are down-regulated in apical periodontitis, offering new insights into this inflammatory disease. This discovery may lead to novel diagnostic and therapeutic strategies for endodontic periapical disease.
Area of Science:
- Endodontics
- Molecular Biology
- Immunology
Background:
- Apical periodontitis is an inflammatory condition of periradicular tissues, stemming from root canal infection and the host immune response.
- MicroRNAs (miRNAs) are known regulators of inflammation and immunity, but their specific role in endodontic periapical disease pathogenesis was unexplored.
Purpose of the Study:
- To investigate the differential expression of miRNAs in diseased periapical tissues compared to healthy controls.
- To identify specific miRNAs involved in the inflammatory processes of apical periodontitis.
Main Methods:
- Microarray analysis was employed to compare miRNA profiles in diseased periapical tissues versus healthy pulps.
- Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) was used to validate the expression of selected miRNAs.
- Target genes of differentially expressed miRNAs were identified using bioinformatics tools (miRWalk, PubMed).
Main Results:
- Microarray analysis identified 381 miRNAs, with 24 found to be significantly down-regulated in diseased tissues (P < .003).
- qRT-PCR confirmed the down-regulation of 7 specific miRNAs in a separate patient cohort (P < .05).
- Identified target genes of these miRNAs include key inflammatory mediators like interleukin-6, matrix metalloproteinase-9, and transforming growth factor-β.
Conclusions:
- The study reveals altered miRNA expression patterns in apical periodontitis, providing novel insights into its pathogenesis.
- These findings hold potential for developing innovative diagnostic markers and therapeutic interventions for apical periodontitis.
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