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Periodontopathic Bacterium<i>Fusobacterium nucleatum</i>Affects Matrix Metalloproteinase-9 Expression in Human Alveolar Epithelial Cells and Mouse Lung

Ryuta Suzuki, Noriaki Kamio, Kozue Sugimoto, Shuichiro Maruoka, Yasuhiro Gon, Tadayoshi Kaneko, Yoshiyuki Yonehara, Kenichi Imai

2022In Vivo19 citationsDOIOpen Access PDF

Abstract

BACKGROUND/AIM: Despite evidence of an association between pulmonary diseases and periodontopathic bacteria, the molecular mechanisms remain unknown. Matrix metalloproteinase-9 (MMP9) plays important roles in pneumonia, chronic obstructive pulmonary disease, and asthma; therefore, we assessed the effects of Fusobacterium nucleatum on MMP9 expression in mouse lung and A549 human alveolar epithelial cells. MATERIALS AND METHODS: Heat-killed F. nucleatum was administered to the trachea of mice or added to A549 cell cultures. MMP9 expression was determined using real-time PCR and western blotting. The involvement of mitogen-activated protein kinases (MAPKs) and nuclear factor-κB (NF-κB) in MMP9 expression was examined. RESULTS: F. nucleatum induced expression of MMP9 in mouse lung and bronchoalveolar lavage fluid. In A549 cells, F. nucleatum induced production of MMP9 protein and mRNA in a density-dependent manner; this was inhibited by inhibitors of extracellular-regulated kinase 1/2 and NF-κB, but not of p38 and Jun N-terminal protein kinase. CONCLUSION: F. nucleatum may contribute to the onset of pulmonary diseases via MMP9 expression through extracellular-regulated kinase 1/2 and NF-κB activation.

Topics & Concepts

Fusobacterium nucleatumMMP9Bronchoalveolar lavageA549 cellKinaseProtein kinase AMolecular biologyBiologyLungCancer researchChemistryDownregulation and upregulationMedicineCell biologyInternal medicineBacteriaPorphyromonas gingivalisBiochemistryGeneGeneticsOral microbiology and periodontitis researchProtease and Inhibitor MechanismsChronic Obstructive Pulmonary Disease (COPD) Research
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