活性氧
上睑下垂
再生(生物学)
细胞外基质
氧化应激
MAPK/ERK通路
变性(医学)
化学
材料科学
信号转导
细胞生物学
细胞凋亡
医学
病理
程序性细胞死亡
生物化学
生物
作者
Hao Zhou,Jinpeng He,Renfeng Liu,Jun Cheng,Yuhao Yuan,Wanpu Mao,J. Zhou,Honghui He,Qianqi Liu,Wei Tan,Cijun Shuai,Youwen Deng
标识
DOI:10.1016/j.bioactmat.2024.02.036
摘要
Intervertebral disc degeneration (IVDD) can be caused by aging, injury, and genetic factors. The pathological changes associated with IVDD include the excessive accumulation of reactive oxygen species (ROS), cellular pyroptosis, and extracellular matrix (ECM) degradation. There are currently no approved specific molecular therapies for IVDD. In this study, we developed a multifunctional and microenvironment-responsive metal-phenolic network release platform, termed TMP@Alg-PBA/PVA, which could treat (IL-1β)-induced IVDD. The metal-phenolic network (TA-Mn-PVP, TMP) released from this platform targeted mitochondria to efficiently scavenge ROS and reduce ECM degradation. Pyroptosis was suppressed through the inhibition of the IL-17/ERK signaling pathway. These findings demonstrate the versatility of the platform. And in a rat model of IVDD, TMP@Alg-PBA/PVA exhibited excellent therapeutic effects by reducing the progression of the disease. TMP@Alg-PBA/PVA, therefore, presents clinical potential for the treatment of IVDD.
科研通智能强力驱动
Strongly Powered by AbleSci AI