Samara C, Syntichaki P, Tavernarakis N
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Heraklion, Crete, Greece.
Cell Death Differ. 2008 Jan;15(1):105-12. doi: 10.1038/sj.cdd.4402231. Epub 2007 Sep 28.
Autophagy is the main process for bulk protein and organelle recycling in cells under extracellular or intracellular stress. Deregulation of autophagy has been associated with pathological conditions such as cancer, muscular disorders and neurodegeneration. Necrotic cell death underlies extensive neuronal loss in acute neurodegenerative episodes such as ischemic stroke. We find that excessive autophagosome formation is induced early during necrotic cell death in C. elegans. In addition, autophagy is required for necrotic cell death. Impairment of autophagy by genetic inactivation of autophagy genes or by pharmacological treatment suppresses necrosis. Autophagy synergizes with lysosomal catabolic mechanisms to facilitate cell death. Our findings demonstrate that autophagy contributes to cellular destruction during necrosis. Thus, interfering with the autophagic process may protect neurons against necrotic damage in humans.
自噬是细胞在细胞外或细胞内应激状态下进行大量蛋白质和细胞器循环利用的主要过程。自噬失调与癌症、肌肉疾病和神经退行性变等病理状况相关。坏死性细胞死亡是急性神经退行性发作(如缺血性中风)中广泛神经元丢失的基础。我们发现,在秀丽隐杆线虫的坏死性细胞死亡早期会诱导过多自噬体形成。此外,坏死性细胞死亡需要自噬。通过自噬基因的遗传失活或药物治疗损害自噬会抑制坏死。自噬与溶酶体分解代谢机制协同作用以促进细胞死亡。我们的研究结果表明,自噬在坏死过程中促成细胞破坏。因此,干扰自噬过程可能保护人类神经元免受坏死性损伤。