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Blumenfeld, L.

Publications and source records attributed to Blumenfeld, L..

2 recordsLinked to original sources

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 Tukeys 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.

molecular biology↗

A Novel Model for Encephalomyosynangiosis Surgery after Middle Cerebral Artery Occlusion-Induced Stroke in Mice

Background and PurposeNo effective treatment is available for most patients who suffer ischemic stroke. Development of novel treatment options is imperative. The brain attempts to self-heal after ischemic stroke via various mechanism mediated by restored blood circulation in affected region of brain but this process is limited by inadequate angiogenesis or neoangiogenesis. Encephalomyosynangiosis (EMS) is a neurosurgical procedure that achieves angiogenesis with low morbidity in patients with moyamoya disease, reducing risk of stroke. However, EMS, surgery has never been studied as an therapeutic option after ischemic stroke. Here we described a novel procedure and feasibility data for EMS after ischemic stroke in mice. MethodsA 60 mins of middle cerebral artery occlusion (MCAo) was used to induce ischemic stroke in mice. After 3-4 hours of MCAo onset/sham, EMS was performed. Mortality of EMS, MCAo and. MCAo+EMS mice was recorded up to 21 days after surgery. Graft tissue viability was measured using a nicotinamide adenine dinucleotide reduced tetrazolium reductase assay. ResultsEMS surgery after ischemic stroke does not increase mortality compared to stroke alone. Graft muscle tissue remained viable 21 days after surgery. ConclusionsThis novel protocol is effective and well-tolerated, may serve as novel platform for new angiogenesis and thus recovery after ischemic stroke. If successful in mice, EMS can a very feasible and novel treatment option for ischemic stroke in humans.

neuroscience↗