铁亡:一种依赖于铁的非阿波性细胞死亡形式
Scott J Dixon1, Kathryn M Lemberg, Michael R Lamprecht
1Department of Biological Sciences, Columbia University, 550 West 120th Street, Northwest Corner Building, MC 4846, New York, NY 10027, USA.
Cell
|May 29, 2012
概括
我们发现了铁亡,一种新的依赖铁的细胞死亡途径,与亡不同. 抑制铁亡可能为癌症和神经退行性疾病提供新的治疗策略.
科学领域:
- 生物化学 生物化学
- 细胞生物学 细胞生物学
- 病理学 病理学 病理学
背景情况:
- 非瘤性细胞死亡机制对于消除瘤细胞和病理条件至关重要.
- 瘤性RAS信号可以诱导特定的细胞死亡途径.
研究的目的:
- 描述一种由小分子埃拉斯诱导的新型的非阿波性细胞死亡.
- 研究这种细胞死亡途径的潜在机制和潜在的治疗影响.
主要方法:
- 使用埃拉斯来诱导癌细胞中的细胞死亡.
- 研究了细胞内铁和抗氧化剂防御的作用.
- 鉴定出铁rostatin-1 作为一种铁灭抑制剂.
- 在大鼠大脑切片中检查了谷氨酸诱导的细胞死亡.
主要成果:
- 埃拉斯诱导一种独特的,依赖于铁的非瘤性细胞死亡,称为铁亡.
- 铁亡在形态学,生化学和遗传学上与亡,亡和自完全不同.
- 费罗斯塔丁-1有效地抑制癌细胞中的铁和谷氨酸诱导的细胞死亡.
- 埃拉斯和谷氨酸通过系统x ((c) ((-) 抑制囊的吸收,耗尽抗氧化防御,导致氧化死亡.
结论:
- 铁亡是一种独特的细胞死亡途径,对于消除某些癌细胞至关重要.
- 抑制铁亡可能提供一种防止神经退行症的保护机制.
相关概念视频
Necrosis
5.4K
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...
5.4K
Overview of Cell Death
8.4K
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...
8.4K
Phagocytosis of Apoptotic Cells
4.2K
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...
4.2K
Autophagic Cell Death
3.7K
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...
3.7K
Apoptosis
12.8K
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...
12.8K
The Early Endosome: Endocytosis of Transferrin
4.3K
Essential proteins such as insulin or low-density lipoprotein (LDL) and micronutrients such as iron enter a eukaryotic cell through receptor-mediated endocytosis. Subsequently, the early endosomes fuse with the vesicles containing such receptor-ligand complexes and play a vital role in sorting the incoming ligands and receptors. While the ligands are either degraded inside the vesicle or released into the cytosol, their receptors are returned to the plasma membrane for further rounds of...
4.3K


