牙龈卟啉单胞菌
毒力
血脑屏障
神经炎症
脂多糖
海马体
毒力因子
微生物学
病态的
医学
神经科学
免疫学
化学
炎症
生物
牙周炎
内科学
中枢神经系统
生物化学
基因
作者
Fulong Li,Chunliang Ma,Shuang Lei,Yaping Pan,Li Lin,Chunling Pan,Qian Li,Fengxue Geng,Dongyu Min,Xiaolin Tang
摘要
Abstract Aim Blood–brain barrier (BBB) disorder is one of the early findings in cognitive impairments. We have recently found that Porphyromonas gingivalis bacteraemia can cause cognitive impairment and increased BBB permeability. This study aimed to find out the possible key virulence factors of P. gingivalis contributing to the pathological process. Materials and Methods C57/BL6 mice were infected with P. gingivalis or gingipains or P. gingivalis lipopolysaccharide ( P. gingivalis LPS group) by tail vein injection for 8 weeks. The cognitive behaviour changes in mice, the histopathological changes in the hippocampus and cerebral cortex, the alternations of BBB permeability, and the changes in Mfsd2a and Cav‐1 levels were measured. The mechanisms of Ddx3x‐induced regulation on Mfsd2a by arginine‐specific gingipain A (RgpA) in BMECs were explored. Results P. gingivalis and gingipains significantly promoted mice cognitive impairment, pathological changes in the hippocampus and cerebral cortex, increased BBB permeability, inhibited Mfsd2a expression and up‐regulated Cav‐1 expression. After RgpA stimulation, the permeability of the BBB model in vitro increased, and the Ddx3x/Mfsd2a/Cav‐1 regulatory axis was activated. Conclusions Gingipains may be one of the key virulence factors of P . gingivalis to impair cognition and enhance BBB permeability by the Ddx3x/Mfsd2a/Cav‐1 axis.
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