Vandenabeele Peter, Vanden Berghe Tom, Festjens Nele
Molecular Signalling and Cell Death Unit, Department for Molecular Biomedical Research, Flanders Interuniversity Institute of Biotechnology (VIB), Ghent, Belgium.
Sci STKE. 2006 Oct 24;2006(358):pe44. doi: 10.1126/stke.3582006pe44.
The use of caspase inhibitors has revealed the existence of alternative backup cell death programs for apoptosis. The broad-spectrum caspase inhibitor zVAD-fmk modulates the three major types of cell death. Addition of zVAD-fmk blocks apoptotic cell death, sensitizes cells to necrotic cell death, and induces autophagic cell death. Several studies have shown a crucial role for the kinase RIP1 and the adenosine nucleotide translocator (ANT)-cyclophilin D (CypD) complex in necrotic cell death. The underlying mechanism of zVAD-fmk-mediated sensitization to necrotic cell death involves the inhibition of caspase-8-mediated proteolysis of RIP1 and disturbance of the ANT-CypD interaction. RIP1 is also involved in autophagic cell death. Caspase inhibitors and knockdown studies have revealed negative roles for catalase and caspase-8 in autophagic cell death. The positive role of RIP1 and the negative role of caspase-8 in both necrotic and autophagic cell death suggest that the pathways of these two types of cell death are interconnected. Necrotic cell death represents a rapid cellular response involving mitochondrial reactive oxygen species (ROS) production, decreased adenosine triphosphate concentration, and other cellular insults, whereas autophagic cell death first starts as a survival attempt by cleaning up ROS-damaged mitochondria. However, when this process occurs in excess, autophagy itself becomes cytotoxic and eventually leads to autophagic cell death. A better understanding of the molecular mechanisms of these alternative cell death pathways may provide therapeutic tools to combat cell death associated with neurodegenerative diseases, ischemia-reperfusion pathologies, and infectious diseases, and may also facilitate the development of alternative cytotoxic strategies in cancer treatment.
半胱天冬酶抑制剂的使用揭示了细胞凋亡存在替代性的备用细胞死亡程序。广谱半胱天冬酶抑制剂zVAD - fmk可调节三种主要类型的细胞死亡。添加zVAD - fmk可阻断凋亡性细胞死亡,使细胞对坏死性细胞死亡敏感,并诱导自噬性细胞死亡。多项研究表明,激酶RIP1和腺苷酸转位酶(ANT)-亲环蛋白D(CypD)复合物在坏死性细胞死亡中起关键作用。zVAD - fmk介导的对坏死性细胞死亡的敏感性的潜在机制涉及抑制半胱天冬酶 - 8介导的RIP1蛋白水解以及干扰ANT - CypD相互作用。RIP1也参与自噬性细胞死亡。半胱天冬酶抑制剂和基因敲低研究揭示了过氧化氢酶和半胱天冬酶 - 8在自噬性细胞死亡中的负面作用。RIP1在坏死性和自噬性细胞死亡中的积极作用以及半胱天冬酶 - 8的负面作用表明这两种类型的细胞死亡途径相互关联。坏死性细胞死亡代表一种快速的细胞反应,涉及线粒体活性氧(ROS)产生、三磷酸腺苷浓度降低和其他细胞损伤,而自噬性细胞死亡最初是作为一种通过清除ROS损伤的线粒体来维持生存的尝试。然而,当这个过程过度发生时,自噬本身就会变得具有细胞毒性并最终导致自噬性细胞死亡。更好地理解这些替代性细胞死亡途径的分子机制可能会提供治疗工具,以对抗与神经退行性疾病、缺血 - 再灌注病理和传染病相关的细胞死亡,也可能促进癌症治疗中替代性细胞毒性策略的发展。