TY - JOUR
T1 - Iron accumulation is associated with periodontal destruction in a mouse model of HFE-related haemochromatosis
AU - Han, Pingping
AU - Liu, Tianqing
AU - Vaquette, Cedryck
AU - Frazer, David
AU - Anderson, Gregory
AU - Ivanovski, Sašo
PY - 2022
Y1 - 2022
N2 - Objective: To investigate the effect of Hfe gene mutation on the distribution of iron and periodontal bone loss in periodontal tissues. Background data: It remains unclear how tissue iron loading affects the periodontium architectures in a genetic animal model of hereditary haemochromatosis (HH). Methods: Male C57BL/6 Hfe−/− (8ÃÂ weeks old) and wild-type (WT) mice were utilized to examine the iron distribution in periodontal tissues, as well as periodontal tissues changes using micro-computed tomography and histomorphometric analysis. Furthermore, tissue inflammatory mediators, bone markers and periodontal pathogens were carried out in PFA-fixed paraffin-embedded tissues using ELISA, RT-qPCR and genomic DNA qPCR, respectively. Results: Excessive iron deposition was found in the periodontal ligament, gingiva and alveolar bone in Hfe−/− mice relative to their WT counterparts. This, in turn, was associated with significant periodontal bone loss, increased cemento-enamel junction-alveolar bone crest distance and decreased expression of molecules involved in bone development and turnover. Furthermore, the pro-inflammatory cytokine - interleukin 6 and periodontal bacteria – Campylobacter rectus were significantly increased in Hfe−/− mice compared with WT controls. Conclusion: Our results suggest that the iron loading in a mouse model of HH decreases alveolar bone formation and leads to alterations in the inflammatory state in the periodontium. Periodontal health should be assessed during the clinical assessment of HFE-HH patients.
AB - Objective: To investigate the effect of Hfe gene mutation on the distribution of iron and periodontal bone loss in periodontal tissues. Background data: It remains unclear how tissue iron loading affects the periodontium architectures in a genetic animal model of hereditary haemochromatosis (HH). Methods: Male C57BL/6 Hfe−/− (8ÃÂ weeks old) and wild-type (WT) mice were utilized to examine the iron distribution in periodontal tissues, as well as periodontal tissues changes using micro-computed tomography and histomorphometric analysis. Furthermore, tissue inflammatory mediators, bone markers and periodontal pathogens were carried out in PFA-fixed paraffin-embedded tissues using ELISA, RT-qPCR and genomic DNA qPCR, respectively. Results: Excessive iron deposition was found in the periodontal ligament, gingiva and alveolar bone in Hfe−/− mice relative to their WT counterparts. This, in turn, was associated with significant periodontal bone loss, increased cemento-enamel junction-alveolar bone crest distance and decreased expression of molecules involved in bone development and turnover. Furthermore, the pro-inflammatory cytokine - interleukin 6 and periodontal bacteria – Campylobacter rectus were significantly increased in Hfe−/− mice compared with WT controls. Conclusion: Our results suggest that the iron loading in a mouse model of HH decreases alveolar bone formation and leads to alterations in the inflammatory state in the periodontium. Periodontal health should be assessed during the clinical assessment of HFE-HH patients.
UR - https://hdl.handle.net/1959.7/uws:67941
U2 - 10.1111/jre.12959
DO - 10.1111/jre.12959
M3 - Article
SN - 0022-3484
VL - 57
SP - 294
EP - 304
JO - Journal of Periodontal Research
JF - Journal of Periodontal Research
IS - 2
ER -