微泡
外体
医学
溃疡性结肠炎
免疫系统
结肠炎
炎症性肠病
炎症
细胞凋亡
癌症研究
药理学
肠粘膜
免疫学
促炎细胞因子
信号转导
口服
小RNA
平衡
先天免疫系统
免疫
再生(生物学)
右旋糖酐
作者
Chao Deng,Xinyi Cheng,Qingying Sun,Yeliaman Yeerbolati,Rui Zheng,Youyi Liu,Yao Ying,Yanbing Shen,Kewei Wang,Jianfeng Huang
标识
DOI:10.1016/j.ijpx.2025.100447
摘要
Restoring intestinal-barrier homeostasis is crucial in treating ulcerative colitis (UC). Milk-derived exosomes, known for their potent biological properties, hold promise in promoting intestinal-barrier repair. However, their stability and targeting ability during gastrointestinal transit remain challenging. To address this, we engineered exosomes via layer-by-layer (LBL) encapsulation, enhancing their stability, controlled release, and targeted delivery. In a C57BL/6 J mouse model of UC induced by dextran sulfate sodium, oral administration of LBL-encapsulated milk-derived exosomes (LBL-Exos) significantly improved the intestinal barrier, including the physical, mucus, and immune barriers, thereby effectively alleviating the symptoms of UC, even at half the exosome dosage. These effects were also associated with reduced apoptosis and inhibition of the PI3K/AKT signaling pathway. This study demonstrates the therapeutic potential of engineered milk-derived exosomes in UC treatment, offering a promising approach for treating colitis and paving the way for the broader use of natural exosomes in related diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI