Eguchi Y, Shimizu S, Tsujimoto Y
Department of Medical Genetics Biomedical Research Center, Osaka University Medical School, Suita.
Rinsho Byori. 1997 May;45(5):470-6.
Apoptosis, a mechanism involving programmed cell death, is important for normal development and maintenance of tissue homeostasis of multicellular organisms. Apoptotic cells are defined by their fragmented nuclei with condensed chromatin, fragmented or condensed cytoplasm and formation of apoptotic bodies. The apoptotic signal transducing pathways activated by a variety of stimuli, including depletion of growth factors, heat shock, cytokines, DNA damaging reagents and crosslinking of Fas receptor, finally converge into the phylogenically conserved apoptotic main machinery, consisting of death-driving ICE-family proteases and anti-cell death protein Bcl-2. Recently, we noted that necrotic cell death induced by chemical hypoxia shares at least some part of the apoptotic main machinery. Using this system, we have shown that Bcl-2 prevents the loss of the mitochondrial membrane potential observed in both apoptotic and necrotic cell death. We also showed that the ICE protease cascade operates in apoptosis and that Bcl-2 functions upstream of the ICE prolease cascade. Here, we review the signal transducing pathway of the apoptotic main machinery.
细胞凋亡是一种涉及程序性细胞死亡的机制,对于多细胞生物体的正常发育和组织稳态的维持至关重要。凋亡细胞的特征在于其细胞核碎片化且染色质浓缩、细胞质碎片化或浓缩以及凋亡小体的形成。由多种刺激激活的凋亡信号转导途径,包括生长因子耗竭、热休克、细胞因子、DNA损伤试剂以及Fas受体交联,最终汇聚到系统发育上保守的凋亡主要机制,该机制由促死亡的ICE家族蛋白酶和抗细胞死亡蛋白Bcl-2组成。最近,我们注意到化学性缺氧诱导的坏死性细胞死亡至少共享凋亡主要机制的某些部分。利用这个系统,我们已经表明Bcl-2可防止在凋亡性和坏死性细胞死亡中观察到的线粒体膜电位丧失。我们还表明ICE蛋白酶级联在凋亡中起作用,并且Bcl-2在ICE蛋白酶级联的上游发挥作用。在此,我们综述凋亡主要机制的信号转导途径。