Jianqiong Pan, Liuqin Teng, Jiaqiong Wu, Xiao Li, Dongdong Zhang, Qingao Meng, Chengkai Zhuang, Ting Chen, Xiahui Lin, Shanni Hong
Idiopathic pulmonary fibrosis (IPF) lacks therapies that reverse disease progression, partly due to persistent senescent alveolar epithelial type II cells (SAEC II). We report a synergistic senolytic strategy combining mitochondrial calcium overload with AKAP1 silencing. An acid-responsive nanoplatform (CCMD@Lipo-Apt) comprising a CaCO3 core co-loaded with curcumin (CUR), Mn2+, and an AKAP1-targeting DNAzyme, enveloped by an L1CAM aptamer-modified lipid bilayer, enables SAEC II-specific homing. Upon lysosomal acidification, CaCO3 degrades to release Ca2+, CUR (mobilizing ER Ca2+), Mn2+, and the DNAzyme. Mn2+ simultaneously activates DNAzyme to knockdown AKAP1 (sensitizing mitochondria to calcium overload) and directly activates caspase-8. This triple mechanism collapses mitochondrial membrane potential and triggers robust apoptosis exclusively in SAEC II. In a bleomycin-induced mouse model, CCMD@Lipo-Apt clears SAEC II, attenuates fibrosis, and restores lung function without overt toxicity. This work establishes a synthetic-lethal axis for targeted IPF therapy.