학술논문

Porphyromonas gingivalis in Alzheimer's disease brains: Evidence for disease causation and treatment with small-molecule inhibitors.
Document Type
article
Source
Science advances. 5(1)
Subject
Brain
Cell Line
Tumor
Saliva
Animals
Mice
Inbred BALB C
Humans
Mice
Porphyromonas gingivalis
Bacteroidaceae Infections
Alzheimer Disease
Disease Models
Animal
Peptide Fragments
tau Proteins
Neuroprotective Agents
Prospective Studies
Pilot Projects
Aged
Middle Aged
Female
Male
Small Molecule Libraries
Amyloid beta-Peptides
Gingipain Cysteine Endopeptidases
Cell Line
Tumor
Inbred BALB C
Disease Models
Animal
Language
Abstract
Porphyromonas gingivalis, the keystone pathogen in chronic periodontitis, was identified in the brain of Alzheimer's disease patients. Toxic proteases from the bacterium called gingipains were also identified in the brain of Alzheimer's patients, and levels correlated with tau and ubiquitin pathology. Oral P. gingivalis infection in mice resulted in brain colonization and increased production of Aβ1-42, a component of amyloid plaques. Further, gingipains were neurotoxic in vivo and in vitro, exerting detrimental effects on tau, a protein needed for normal neuronal function. To block this neurotoxicity, we designed and synthesized small-molecule inhibitors targeting gingipains. Gingipain inhibition reduced the bacterial load of an established P. gingivalis brain infection, blocked Aβ1-42 production, reduced neuroinflammation, and rescued neurons in the hippocampus. These data suggest that gingipain inhibitors could be valuable for treating P. gingivalis brain colonization and neurodegeneration in Alzheimer's disease.