活性氧
程序性细胞死亡
串扰
细胞生物学
细胞命运测定
炎症
生物
氧化还原
细胞
化学
细胞存活
氧气
调节器
平衡(能力)
细胞凋亡
中心性
信号转导
生物物理学
作者
Noah Sendtner,Rebecca Seitz,Noah Brandl,Martina Müller,Karsten Gülow
标识
DOI:10.3390/ijms262010240
摘要
Reactive oxygen species (ROS) are versatile determinants of cell fate, tipping the balance between survival and death. By exceeding critical thresholds or perturbing compartment-specific signaling, ROS can initiate, modulate, or suppress regulated cell death (RCD). Importantly, their influence extends across the full spectrum of currently characterized RCD modalities. 19 distinct forms of cell death-including both long-established and recently described entities-are shaped by ROS, either as triggers, modulators, or inhibitors. Beyond pathway-specific effects, ROS promote crosstalk between death programs, enabling switches from one mode to another and determining whether outcomes are inflammatory or non-inflammatory. By systematically integrating 19 RCD types, the unifying role of ROS emerges as both gatekeeper and connector of diverse death pathways. Such a comprehensive perspective underscores the centrality of redox imbalance in cell fate control and highlights its broader implications for inflammation and disease.
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