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It's All in the PAN: Crosstalk, Plasticity, Redundancies, Switches, and Interconnectedness Encompassed by PANoptosis Underlying the Totality of Cell Death-Associated Biological Effects

期刊

CELLS
卷 11, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/cells11091495

关键词

PANoptosis; PANoptosome; pyroptosis; apoptosis; necroptosis; inflammatory cell death; inflammasome; inflammation; innate immunity; infection; NLR; caspase; IRF1; ZBP1; RIPK1; RIPK3; MLKL; NLRP3; AIM2; Pyrin; caspase-1; ASC; caspase-8; caspase-3; caspase-7; crosstalk; plasticity; redundancy

资金

  1. National Institutes of Health [AI101935, AI124346, AI160179, AR056296, CA253095]
  2. American Lebanese Syrian Associated Charities

向作者/读者索取更多资源

The article discusses the cell death pathways and their interactions in the innate immune system. By viewing them through the lens of an integrated inflammatory cell death concept called PANoptosis, the diverse descriptions of interactions can be better understood. The article also introduces PANoptosomes as multifaceted macromolecular complexes regulating PANoptosis, and highlights the importance of PANoptosis in infections, diseases, and cancers. Having a holistic understanding of cell death is crucial for identifying new therapeutic strategies.
The innate immune system provides the first line of defense against cellular perturbations. Innate immune activation elicits inflammatory programmed cell death in response to microbial infections or alterations in cellular homeostasis. Among the most well-characterized programmed cell death pathways are pyroptosis, apoptosis, and necroptosis. While these pathways have historically been defined as segregated and independent processes, mounting evidence shows significant crosstalk among them. These molecular interactions have been described as 'crosstalk', 'plasticity', 'redundancies', 'molecular switches', and more. Here, we discuss the key components of cell death pathways and note several examples of crosstalk. We then explain how the diverse descriptions of crosstalk throughout the literature can be interpreted through the lens of an integrated inflammatory cell death concept, PANoptosis. The totality of biological effects in PANoptosis cannot be individually accounted for by pyroptosis, apoptosis, or necroptosis alone. We also discuss PANoptosomes, which are multifaceted macromolecular complexes that regulate PANoptosis. We consider the evidence for PANoptosis, which has been mechanistically characterized during influenza A virus, herpes simplex virus 1, Francisella novicida, and Yersinia infections, as well as in response to altered cellular homeostasis, in inflammatory diseases, and in cancers. We further discuss the role of IRF1 as an upstream regulator of PANoptosis and conclude by reexamining historical studies which lend credence to the PANoptosis concept. Cell death has been shown to play a critical role in infections, inflammatory diseases, neurodegenerative diseases, cancers, and more; therefore, having a holistic understanding of cell death is important for identifying new therapeutic strategies.

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