Yin Jiali, Xu Xinjun, Guo Ying, Sun Caiyu, Yang Yujuan, Liu Huifang, Yu Pengyi, Wu Tong, Song Xicheng
Department of Otolaryngology, Head and Neck Surgery, Yantai Yuhuangding Hospital, Qingdao University, Yantai, China.
Shandong Provincial Key Laboratory of Neuroimmune Interaction and Regulation, Yantai, Shandong, China.
Cell Death Discov. 2024 Oct 2;10(1):424. doi: 10.1038/s41420-024-02181-2.
As common clinical-pathological processes, wound healing and tissue remodelling following injury or stimulation are essential topics in medical research. Promoting the effective healing of prolonged wounds, improving tissue repair and regeneration, and preventing fibrosis are important and challenging issues in clinical practice. Ferroptosis, which is characterized by iron overload and lipid peroxidation, is a nontraditional form of regulated cell death. Emerging evidence indicates that dysregulated metabolic pathways and impaired iron homeostasis play important roles in various healing and regeneration processes via ferroptosis. Thus, we review the intrinsic mechanisms of tissue repair and remodeling via ferroptosis in different organs and systems under various conditions, including the inflammatory response in skin wounds, remodeling of joints and cartilage, and fibrosis in multiple organs. Additionally, we summarize the common underlying mechanisms, key molecules, and targeted drugs for ferroptosis in repair and regeneration. Finally, we discuss the potential of therapeutic agents, small molecules, and novel materials emerging for targeting ferroptosis to promote wound healing and tissue repair and attenuate fibrosis.
作为常见的临床病理过程,损伤或刺激后的伤口愈合和组织重塑是医学研究的重要课题。促进长期伤口的有效愈合、改善组织修复和再生以及预防纤维化是临床实践中的重要且具有挑战性的问题。铁死亡以铁过载和脂质过氧化为特征,是一种非传统形式的程序性细胞死亡。新出现的证据表明,代谢途径失调和铁稳态受损通过铁死亡在各种愈合和再生过程中发挥重要作用。因此,我们综述了在各种条件下不同器官和系统中通过铁死亡进行组织修复和重塑的内在机制,包括皮肤伤口的炎症反应、关节和软骨的重塑以及多个器官的纤维化。此外,我们总结了修复和再生中铁死亡的共同潜在机制、关键分子和靶向药物。最后,我们讨论了新兴的靶向铁死亡以促进伤口愈合和组织修复并减轻纤维化的治疗药物、小分子和新型材料的潜力。