Hyperactivation of Mincle in exacerbated apical periodontitis in an autoinflammatory mouse model for cherubism

Aims: To examine the role of Mincle, a C-type lectin (Clec) pathogen recognition receptor (PRR), in exacerbated apical periodontitis (AP) in an autoinflammatory mouse model for cherubism (CBM). Methodology: Patients with immune system dysfunction have higher prevalence of AP but the mechanism remains largely unknown. We studied a knock-in (KI) mouse model carrying a Sh3bp2 mutation for CBM. We performed pulp exposure in one lower 1st molar of 5- to 6-week-old mice to introduce pathogen-associated molecular patterns (PAMP)-induced endodontic infection. We determined the expression levels of Clec subfamily genes by qPCR. To suppress Mincle, we generated Sh3bp2+/+Mincle+/+, Sh3bp2+/KIMincle+/+, and Sh3bp2+/KIMincleKO/KO mice or injected Sh3bp2+/KI mice with a Mincle-binding DNA aptamer (AptMincle). Mice were analyzed 42 days after pulp exposure by micro-CT (mCT), qPCR and immunoblotting. Statistical analysis was performed by one-way ANOVA followed by post-hoc analysis with Tukey’s test or two-way ANOVA followed by Sidak correction. p < 0.05 was considered statistically significant. Results: Expression of Clec4e (Mincle) was significantly increased in Sh3bp2 mutant mice after pulp exposure compared to WT littermates (p<0.0001). Sh3bp2+/KIMincle+/+ and Sh3bp2+/KIMincleKO/KO mice had a comparable response to pulp exposure, including the degree of bone loss and induction of inducible NOS (iNOS), IL-1b, and TNF-a. Sh3bp2+/KI mice injected with AptMincle after pulp exposure for 21 days showed significant amelioration of bone loss compared to mice with vehicle injection (p<0.0001). Conclusions: These seemingly conflicting data of suppressing Mincle by crossing with Mincle KO mice and AptMincle injection suggest that Mincle has dual functions upon PAMPs stimulation, consistent with a previous study showing that Mincle enhances tissue destruction during the inflammatory stage and is subsequently needed for inflammation resolution. Fine-tuned suppression of Mincle significantly reduces the severity of AP in Sh3bp2+/KI mice. This study suggests that patients with CBM may benefit from more frequent dental examinations and early intervention to reduce or prevent severe progressive bone loss in periapical tissues.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-11
DOI
https://doi.org/10.64898/2026.11.09.765482
Primary Topic
Endodontics and Root Canal Treatments
Type
preprint
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preprint

Hyperactivation of Mincle in exacerbated apical periodontitis in an autoinflammatory mouse model for cherubism

Leslie Blumenfeld, Yasuyoshi Ueki, Ernst Reichenberger, Adam Kim et al.
bioRxiv (Cold Spring Harbor Laboratory)
Endodontics and Root Canal Treatments
preprint

Hyperactivation of Mincle in exacerbated apical periodontitis in an autoinflammatory mouse model for cherubism

Leslie Blumenfeld, Yasuyoshi Ueki, Ernst Reichenberger, Adam Kim, Eisaku Nishida, Ayano Hatori, I‐Ping Chen, Daniel Faissal Kotait, Kiseki Washitani
preprint en

Abstract

Aims: To examine the role of Mincle, a C-type lectin (Clec) pathogen recognition receptor (PRR), in exacerbated apical periodontitis (AP) in an autoinflammatory mouse model for cherubism (CBM). Methodology: Patients with immune system dysfunction have higher prevalence of AP but the mechanism remains largely unknown. We studied a knock-in (KI) mouse model carrying a Sh3bp2 mutation for CBM. We performed pulp exposure in one lower 1st molar of 5- to 6-week-old mice to introduce pathogen-associated molecular patterns (PAMP)-induced endodontic infection. We determined the expression levels of Clec subfamily genes by qPCR. To suppress Mincle, we generated Sh3bp2+/+Mincle+/+, Sh3bp2+/KIMincle+/+, and Sh3bp2+/KIMincleKO/KO mice or injected Sh3bp2+/KI mice with a Mincle-binding DNA aptamer (AptMincle). Mice were analyzed 42 days after pulp exposure by micro-CT (mCT), qPCR and immunoblotting. Statistical analysis was performed by one-way ANOVA followed by post-hoc analysis with Tukey’s test or two-way ANOVA followed by Sidak correction. p < 0.05 was considered statistically significant. Results: Expression of Clec4e (Mincle) was significantly increased in Sh3bp2 mutant mice after pulp exposure compared to WT littermates (p<0.0001). Sh3bp2+/KIMincle+/+ and Sh3bp2+/KIMincleKO/KO mice had a comparable response to pulp exposure, including the degree of bone loss and induction of inducible NOS (iNOS), IL-1b, and TNF-a. Sh3bp2+/KI mice injected with AptMincle after pulp exposure for 21 days showed significant amelioration of bone loss compared to mice with vehicle injection (p<0.0001). Conclusions: These seemingly conflicting data of suppressing Mincle by crossing with Mincle KO mice and AptMincle injection suggest that Mincle has dual functions upon PAMPs stimulation, consistent with a previous study showing that Mincle enhances tissue destruction during the inflammatory stage and is subsequently needed for inflammation resolution. Fine-tuned suppression of Mincle significantly reduces the severity of AP in Sh3bp2+/KI mice. This study suggests that patients with CBM may benefit from more frequent dental examinations and early intervention to reduce or prevent severe progressive bone loss in periapical tissues.

bioRxiv (Cold Spring Harbor Laboratory)
University of Connecticut (US), University of Dental Medicine (MM), Indiana University (US), UConn Health (US)
Endodontics and Root Canal Treatments
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