肺纤维化
先天免疫系统
生物
巨噬细胞
特发性肺纤维化
自噬
肺泡巨噬细胞
粒体自噬
免疫系统
免疫学
纤维化
细胞凋亡
免疫
肺
癌症研究
重编程
获得性免疫系统
线粒体
间质性肺病
信号转导
表观遗传学
CCL18型
肌成纤维细胞
支气管肺泡灌洗
程序性细胞死亡
作者
Xinru Wang,Xinya Guo,Huiwen Meng,Zhiheng Sun
出处
期刊:Biology
[Multidisciplinary Digital Publishing Institute]
日期:2026-08-11
卷期号:15 (16): 1366-1366
标识
DOI:10.3390/biology15161366
摘要
Trained immunity (TI) represents a form of immune memory in innate immune cells, driven by sustained epigenetic and metabolic reprogramming that potentiates innate immune responses. Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease characterized by persistent alveolar injury and pathological tissue remodeling. Given the central role of macrophages in IPF pathogenesis, we hypothesized that inducing TI could functionally reprogram these cells and attenuate fibrosis. In a murine model of pulmonary fibrosis induced by bleomycin, prior induction of TI via β-glucan enhanced autophagic activity in macrophages and reduced pathological collagen deposition. This trained response restricted bleomycin-triggered mitochondrial DNA release and suppressed the mitochondrial apoptosis pathway, thereby promoting macrophage survival. The protective effects were diminished by administration of the AMPK inhibitor Compound C. Our findings indicate that TI promotes mitophagy correlating with the AMPK-ULK1 signaling axis, thereby reducing alveolar macrophage apoptosis and uncovering a potential therapeutic strategy for pulmonary fibrosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI