SREBP activation contributes to fatty acid accumulations in necroptosis. Issue 4 (21st February 2023)

• Record Type: Journal Article
• Authors: Lu, Daniel; Parisi, Laura R.; Gokcumen, Omer; Atilla-Gokcumen, G. Ekin
• Is Part Of: RSC chemical biology. Volume 4:Issue 4(2023)
• Page Start: 310
• Page End: 322
• Publication Date: 2023-02-21
• Subjects: 572
• DOI: 10.1039/d2cb00172a
• Languages: English
• ISSNs: 2633-0679

Abstract

Abstract : .Necroptosis is accompanied by accumulation of lipids. This study shows that SREBPs are activated and cause increase in the production of very long-chain fatty acids during necroptosis. Abstract : Necroptosis is a type of programmed cell death. It is characterized by membrane permeabilization and is associated with the release of intracellular components due to compromised membrane integrity which induces a strong inflammatory response. We recently showed that the accumulation of very long chain fatty acids (VLCFAs) contributes to membrane permeabilization during necroptosis. However, the mechanisms that result in the accumulation of these cytotoxic lipids remain unknown. Using comparative transcriptomics and digital PCR validations, we found that several target genes of sterol regulatory element-binding proteins (SREBPs) were upregulated during necroptosis, suggesting that they might be responsible for the accumulation of VLCFA in this process. We demonstrated that activation of SREBPs during necroptosis exacerbates the permeability of the plasma membrane and cell death. Consistent with these observations, targeting sterol regulatory element-binding protein cleavage-activating protein (SCAP), a protein involved in SREBP activation, reversed the accumulation of VLCFAs, and restored cell death and membrane permeabilization during necroptosis. Collectively, our results highlight a role for SREBP in regulating lipid changes during necroptosis and suggest SREBP-mediated lipid remodeling as a potential target for therapeutics to reduce membrane permeabilization during necroptosis.