Apoptotic Caspases Suppress mtDNA-Induced STING-Mediated Type I IFN Production

作者：White, Michael J.^*; McArthur, Kate; Metcalf, Donald; Lane, Rachael M.; Cambier, John C.; Herold, Marco J.; van Delft, Mark F.; Bedoui, Sammy; Lessene, Guillaume; Ritchie, Matthew E.; Huang, David C. S.; Kile, Benjamin T.

来源：Cell, 2014, 159(7): 1549-1562.

DOI：10.1016/j.cell.2014.11.036

• HEMATOPOIETIC STEM-CELLS
• ACTIVATION
• DNA
• REPOPULATION
• PROTEINS
• NECROSIS
• FAMILY
• ALPHA
• MCL-1
• BRAIN

Activated caspases are a hallmark of apoptosis induced by the intrinsic pathway, but they are dispensable for cell death and the apoptotic clearance of cells in vivo. This has led to the suggestion that caspases are activated not just to kill but to prevent dying cells from triggering a host immune response. Here, we show that the caspase cascade suppresses type I interferon (IFN) production by cells undergoing Bak/Bax-mediated apoptosis. Bak and Bax trigger the release of mitochondrial DNA. This is recognized by the cGAS/STING-dependent DNA sensing pathway, which initiates IFN production. Activated caspases attenuate this response. Pharmacological caspase inhibition or genetic deletion of caspase-9, Apaf-1, or caspase-3/7 causes dying cells to secrete IFN-beta. In vivo, this precipitates an elevation in IFN-beta levels and consequent hematopoietic stem cell dysfunction, which is corrected by loss of Bak and Bax. Thus, the apoptotic caspase cascade functions to render mitochondrial apoptosis immunologically silent.

• 出版日期2014-12-18
• 单位河北医科大学