一本关于细胞死亡途径的指南
Junying Yuan1,2, Dimitry Ofengeim3
1Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Shanghai, China. junying_yuan@sioc.ac.cn.
Nature reviews. Molecular cell biology
|December 19, 2023
概括
编程细胞死亡,包括亡,亡和亡,在健康和疾病中至关重要. 本综述详细介绍了主要的细胞死亡机制,它们的调节和疾病相关性.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 病理学 病理学 病理学
背景情况:
- 调节细胞死亡,或编程细胞死亡,对于生物体的健康和疾病过程至关重要.
- 关键的编程细胞死亡途径包括亡,亡和亡,每一个都涉及不同的分子机械.
- 细胞平衡中断也可以触发非编程细胞死亡,如兴奋毒性,铁亡和溶酶体细胞死亡.
研究的目的:
- 提供关于主要细胞死亡机制的全面概述.
- 突出了解这些途径的复杂监管和执行的最新进展.
- 讨论不同细胞死亡模式在人类疾病中的相关性.
主要方法:
- 审查现有的关于编程和非编程细胞死亡的文献.
- 对参与细胞死亡的分子调节器和信号通路的分析.
- 整合与细胞死亡的病理影响相关的发现.
主要成果:
- 亡包括酶级联,而亡依赖于酶激活的气体皮膜形成膜孔.
- 亡是一种由RIPK3和MLKL调节的caspase独立途径,由caspase-8抑制.
- 非编程细胞死亡模式是由细胞平衡中断引起的,影响离子平衡,氧化还原状态和 lysosomal 功能.
结论:
- 了解复杂的细胞死亡途径网络对于破译疾病发病因子至关重要.
- 针对特定的细胞死亡机制对各种人类疾病具有治疗潜力.
- 进一步研究不同细胞死亡模式之间的相互作用将推动这一领域的发展.
更多相关视频
相关概念视频
Overview of Cell Death
7.3K
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...
7.3K
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
The Extrinsic Apoptotic Pathway
6.4K
The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
6.4K
Necrosis
4.5K
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...
4.5K
Apoptosis
11.5K
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...
11.5K
The Intrinsic Apoptotic Pathway
6.6K
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...
6.6K


