铁亡:当新陈代谢遇到细胞死亡时
Jiashuo Zheng1, Marcus Conrad1,2
1Institute of Metabolism and Cell Death, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.
Physiological reviews
|December 11, 2024
概括
铁亡是一种受调节的细胞死亡,与新陈代谢密切相关. 这篇评论详细介绍了其代谢驱动因素,监控系统以及在衰老,疾病和癌症治疗中的作用.
科学领域:
- 生物化学 生物化学
- 细胞生物学 细胞生物学
- 代谢调节 代谢调节 代谢调节 代谢调节
背景情况:
- 铁亡是一种独特的,依赖于铁的受调细胞死亡形式.
- 最近的研究揭示了它在各种生理和病理过程中的关键作用.
研究的目的:
- 为了提供关于铁亡的全面更新.
- 为了强调其代谢基础和生理影响.
- 探索其在癌症等疾病中的治疗潜力.
主要方法:
- 文献综述和关键研究的批判性评价关于ferroptosis.
- 分析影响铁亡的代谢途径,包括微量元素,氨基酸,碳水化合物和脂质.
- 检查铁灭菌监测系统和监管机制.
主要成果:
- 铁代谢受铁,,氨基酸,碳水化合物,胆固醇和脂肪酸等复杂的代谢网络的调节.
- 关键的监测系统包括囊胺/谷氨/GPX4轴,NAD/P) H/FSP1/CoQ系统和GTPCH1/BH4轴.
- 铁致死在衰老,瘤抑制,感染,缺血-再输液损伤和神经退行等方面发挥着重要作用.
结论:
- 代谢失调是ferroptosis的核心.
- 了解铁亡途径为癌症和其他疾病提供了治疗途径.
- 对于临床应用来说,对铁灭调节剂的进一步研究至关重要.
相关概念视频
Necrosis
4.3K
Necrosis is considered as an “accidental” or unexpected form of cell death that ends in cell lysis. The first noticeable mention of “necrosis” was in 1859 when Rudolf Virchow used this term to describe advanced tissue breakdown in his compilation titled “Cell Pathology”.
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become...
4.3K
Overview of Cell Death
7.0K
Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the...
7.0K
Autophagic Cell Death
3.4K
Christian de Duve discovered “autophagy,” a process in which cellular components are engulfed by membrane-bound organelles called autophagosomes. The autophagosomes then fuse with lysosomes to digest the enclosed contents. Autophagy is generally activated in cells to prevent cell death. However, cell death is triggered when the damage is beyond repair.
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
3.4K
Apoptosis
11.2K
Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size...
11.2K
Phagocytosis of Apoptotic Cells
3.7K
Cells undergoing apoptosis form apoptotic bodies that must be removed immediately to prevent inflammation, autoimmune diseases, and necrosis. Phagocytosis is carried out by professional phagocytes such as macrophages or immature dendritic cells. Non-professional phagocytes such as epithelial cells and fibroblasts also take part in this process; however, they are not as effective as professional phagocytes.
Normal cells contain receptors that prevent them from being recognized...
Normal cells contain receptors that prevent them from being recognized...
3.7K
The Intrinsic Apoptotic Pathway
6.4K
Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
6.4K


