Citation
- Authors: Liu Q. et al.
- Year: 2021
- Journal: Cell Death Dis 12 673
- Applications: in vitro / DNA, siRNA / INTERFERin
- Cell types:
- Name: Mouse bone marrow-derived macrophages
Description: Primary mouse bone marrow macrophages
Known as: BMDM - Name: RAW 264.7
Description: Mouse monocytes/macrophages
Known as: RAW
- Name: Mouse bone marrow-derived macrophages
Method
Cultured cells seeded in six-well plates with microscope cover glasses were transfected for 24 h with pMRX-IP-GFP-LC3-RFP-LC3ΔG using INTERFERin (409-10, Polyplus).
The cells were treated with Sal.
Autophagy was then measured by counting cells in GFP-LC3 puncta or GFP+/RFP+ and GFP-/RFP-LC3+ puncta with confocal microscope.
Cells were transfected with control siRNA or TBK1 siRNA 24 h before control or DMXAA treatment.
Abstract
The STING pathway and its induction of autophagy initiate a potent immune defense response upon the recognition of pathogenic DNA. However, this protective response is minimal, as STING activation worsens organ damage, and abnormal autophagy is observed during progressive sepsis. Whether and how the STING pathway affects autophagic flux during sepsis-induced acute lung injury (sALI) are currently unknown. Here, we demonstrate that the level of circulating mtDNA and degree of STING activation are increased in sALI patients. Furthermore, STING activation was found to play a pivotal role in mtDNA-mediated lung injury by evoking an inflammatory storm and disturbing autophagy. Mechanistically, STING activation interferes with lysosomal acidification in an interferon (IFN)-dependent manner without affecting autophagosome biogenesis or fusion, aggravating sepsis. Induction of autophagy or STING deficiency alleviated lung injury. These findings provide new insights into the role of STING in the regulatory mechanisms behind extrapulmonary sALI.