Caspases, traditionally viewed as mediators of apoptosis and tumor suppressors, have also been shown to promote cell proliferation and to contribute to tumor growth. For example, the initiator caspase Dronc (the Drosophila orthologue of Caspase-9) can trigger apoptosis-induced proliferation (AiP), a process where apoptotic cells generate mitogenic signals for compensatory proliferation independently of their apoptotic function. AiP is crucial for homeostatic cell turnover, wound healing, and tissue regeneration. Previously, we established that Dronc activates the NADPH oxidase DUOX at the plasma membrane, resulting in the production of extracellular reactive oxygen species (ROS) which are required for AiP. However, the mechanism by which Dronc activates DUOX has remained elusive. Here, we identified Dronc-dependent Ca 2+ entry into the cytosol as a significant factor for DUOX activation and AiP. Three cell surface Ca 2+ channels of the TRP family mediate Ca 2+ influx in a non-redundant fashion. Additionally, calcium-induced calcium release (CICR) from the ER was identified as another source of cytosolic Ca 2+ during AiP. Notably, DUOX itself acts as a Ca 2+ effector in AiP, requiring Ca 2+ binding for its activation. These findings highlight the importance of Ca 2+ signaling in AiP and provide insights into how similar signaling mechanisms might operate in vertebrates.
Suthar et al. (Tue,) studied this question.