Abstract

Non-apoptotic regulated cell death (RCD) is essential to maintain organismal homeostasis and may be aberrantly activated during certain pathological states. Lipids are emerging as key components of several non-apoptotic RCD pathways. For example, a direct interaction between membrane phospholipids and the pore-forming protein mixed lineage kinase domain-like (MLKL) is needed for the execution of necroptosis, while the oxidative destruction of membrane polyunsaturated fatty acids (PUFAs), following the inactivation of glutathione peroxidase 4 (GPX4), is a requisite gateway to ferroptosis. Here, we review the roles of lipids in the initiation and execution of these and other forms of non-apoptotic cell death. We also consider new technologies that are allowing for the roles of lipids and lipid metabolism in RCD to be probed in increasingly sophisticated ways. In certain cases, this new knowledge may enable the development of therapies that target lipids and lipid metabolic processes to enhance or suppress specific non-apoptotic RCD pathways.

Highlights

  • Emerging evidence suggests important roles for lipids and lipid metabolism in several non-apoptotic cell death pathways

  • The precise target and mechanism of action of this lethal compound remains to be resolved, these results suggest that small molecule-mediated perturbations of fatty acids (FAs) metabolism can cause non-apoptotic Regulated cell death (RCD)

  • SREBP1/2 upregulates transcription of Fatty acid synthase (FASN) and HMGCR, resulting in the accumulation of cholesterol and other lipids.[78]

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Summary

Open Questions

What molecular mechanisms link the accumulation of specific lipids to the induction of non-apoptotic RCD?. One possibility is that p53-dependent effects on lipid metabolism could modulate ferroptosis sensitivity by altering lipid metabolism or membrane lipid composition

Challenges and open questions
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