https://ror.org/023rffy11 Laboratory for Homeodynamics, RIKEN BDR, Kobe, Japan.
Division of Developmental Biology and Regenerative Medicine, Kobe University, Kobe, Japan.
Life Sci Alliance. 2024 Jan 31;7(4). doi: 10.26508/lsa.202302238. Print 2024 Apr.
Cell death and proliferation are at a glance dichotomic events, but occasionally coupled. Caspases, traditionally known to execute apoptosis, play non-apoptotic roles, but their exact mechanism remains elusive. Here, using intestinal stem cells (ISCs), we discovered that activation of caspases induces massive cell proliferation rather than cell death. We elucidate that a positive feedback circuit exists between caspases and JNK, which can simultaneously drive cell proliferation and cell death. In ISCs, signalling from JNK to caspases is defective, which skews the balance towards proliferation. Mechanistically, two-tiered regulation of the DIAP1 inhibitor , through its transcription and its protein localization, exists. This work provides a conceptual framework that explains how caspases perform apoptotic and non-apoptotic functions in vivo and how ISCs accomplish their resistance to cell death.
细胞死亡和增殖乍一看是二分法事件,但偶尔也会偶联。传统上已知细胞凋亡执行 caspase,但它们的非凋亡作用的确切机制仍然难以捉摸。在这里,我们使用肠干细胞 (ISCs) 发现 caspase 的激活诱导大量细胞增殖而不是细胞死亡。我们阐明 caspase 和 JNK 之间存在正反馈回路,它可以同时驱动细胞增殖和细胞死亡。在 ISCs 中,JNK 到 caspase 的信号传导存在缺陷,这使平衡偏向增殖。从机制上讲,通过其转录和蛋白质定位,对 DIAP1 抑制剂存在两层调节。这项工作提供了一个概念框架,解释了 caspase 如何在体内执行凋亡和非凋亡功能,以及 ISC 如何抵抗细胞死亡。