基质金属蛋白酶
牙周炎
促炎细胞因子
巨噬细胞极化
脂多糖
巨噬细胞
炎症
先天免疫系统
化学
免疫学
医学
免疫系统
牙科
内科学
体外
生物化学
作者
Tong Zhao,Zhuangzhuang Chu,Catherine Huihan Chu,Shuo Dong,Guoqing Li,Jin Wu,Chunbo Tang
标识
DOI:10.3389/fimmu.2023.1194662
摘要
Macrophages are an integral part of the innate immune response in periodontal tissue and play a crucial role in the progression of periodontitis. Here we reported that macrophages also provoke periodontitis-induced gingival destruction through Piezol-mediated collagen degradation. We discovered that the PIEZO1 expression was markedly elevated in patients with periodontitis through transcriptomic profiling. Moreover, Piezo1 promoted macrophage polarization toward the M1 type in response to lipopolysaccharide (LPS) and induced production of proinflammatory cytokines, which in turn stimulated production of matrix metalloproteinases (MMPs) leading to collagen degradation. Our study suggests that Piezol might be a potential therapeutic target for treating periodontitis-induced gingival destruction.
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