铁蛋白
肺纤维化
肌成纤维细胞
细胞外基质
医学
纤维化
肺
病理
生物标志物
病态的
癌症研究
免疫学
发病机制
特发性肺纤维化
基因敲除
矽肺
成纤维细胞
半乳糖凝集素-3
细胞外
疾病
体内
博莱霉素
调解人
作者
Liqun Wang,Xuxi Chen,Hongying Quan,Rui Qian,Shuyu Gong,Qiurong He,Ying Gao,Ajia Axi,Manyu Zhao,Hao Xu,Ling Zhang,Lijun Peng,Xin Sun,Ben Zhang,Yuqin Yao
标识
DOI:10.1002/advs.202519191
摘要
Silicosis is a progressive and life-threatening fibrotic lung disease caused by crystalline silica. However, targeted therapies remain unavailable due to its incompletely understood pathogenic mechanisms. Here, we identify ferritin as a pivotal mediator of silica-induced pulmonary fibrosis by integrating clinical exploration with experimental validation. We detected persistently elevated ferritin levels in lung tissues and serum from silicosis patients and silica-exposed mice, and demonstrated that exogenous ferritin administration exacerbates fibrosis in vivo. Multi-omics profiling and co-culture experiments revealed that macrophage-secreted ferritin promotes fibroblast-to-myofibroblast differentiation and pathological extracellular matrix (ECM) deposition via the PIK3R2/SMAD signaling axis. Importantly, genetic knockdown of ferritin in macrophages significantly suppressed myofibroblast differentiation and collagen accumulation both in vivo and in vitro. These findings underscore that ferritin functions not only as a potential clinical biomarker for silicosis surveillance but also as a pathogenic driver through macrophage-fibroblast crosstalk, and provide a theoretical foundation for developing integrated diagnostic and therapeutic strategies against silicosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI