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A matter of life and death for caspase 8

Cells can control their own death as part of normal development or in response to pathogens and toxins. Although apoptosis allows the non-inflammatory clearance of cells from the body, other forms of programmed cell death, including necroptosis and pyroptosis, induce an inflammatory response to intracellular pathogens.

Credit: Neil Smith/Springer Nature Limited

Programmed cell death is mediated by caspase cysteine proteases such as caspase 8, which can mediate extrinsic apoptosis and suppress necroptosis by inhibiting the kinases RIPK1/RIPK3 and the pseudokinase MLKL.

Now, studies by Fritsch et al. and Newton et al., both published in Nature, describe an additional role for caspase 8 in mediating pyroptosis when apoptosis and necroptosis are inhibited.

Both groups found that expression of a catalytically inactive caspase 8 was lethal to mice at embryonic day (E)11.5 and used different models to look for the cause of embryonic lethality. Fritsch et al. expressed caspase 8 with a point mutation in its substrate binding pocket (Casp8C362S/fl) in epidermal keratinocytes and in intestinal epithelial cells (using Krt14cre and Villincre drivers, respectively). These mice were viable but experienced necroptosis in these tissues. Suppression of necroptosis through deletion of Mlkl rescued the skin phenotype but worsened the inflammatory destruction of the intestine, leading to premature death of Casp8C362S/fl Villincre mice at 4 weeks of age. Moreover, Casp8C362S/362S mice deficient in the necroptosis mediator RIPK3, while not showing embryonic lethality, were dramatically stunted, suggesting a necroptosis-independent role for inactive caspase 8. The authors examined soluble proteins in the ileum of Casp8C362S/fl Villincre Mlk−/− mice and found high levels of IL-1β and the active cleaved version of the executioner caspase caspase 1. Cleavage of caspase 1 and IL-1β are signs of pyroptotic cell death, suggesting pyroptosis of ileal epithelial cells in the absence of necroptosis.

In a concurrent study, Newton et al. showed that knockout of Mlkl in mice with a catalytically inactive caspase 8 (Casp8C362A/C362A) reversed embryonic death, but caused death during the perinatal period. Early embryos of Casp8362A/362A Mlkl−/− mice expressed higher levels of inflammatory cytokines in the gut than Casp8−/− Mlk−/− embryos. Using multiple knockout models to investigate the role of caspase 1, caspase 11 and the necroptosis protein RIPK3 in the Casp8C362A/C362A Mlkl−/− phenotype, the authors found caspase 1 to be a major driver for perinatal lethality in Casp8C362A/C362A Mlkl−/− mice, with caspase 11 contributing to death around weaning. These data suggest that pyroptosis mediates perinatal death. Although caspase 1 was driving lethality, knockout of the pyroptosis pore-forming protein and caspase 1 substrate gasdermin D did not rescue Casp8C362A/C362A Mlkl−/− mice from dying shortly after birth, suggesting that cleavage of other caspase 1 substrates, such as caspase 3 or caspase 7, may drive perinatal lethality.

Both studies found that the expression of inactive caspase 8 or pan-caspase inhibition induced the formation of apoptosis-associated speck-like protein containing a CARD (ASC) specks and subsequent caspase 1 activation. Each group also showed that deletion of ASC or caspase 1 rescued perinatal lethality in caspase 8 activity-deficient Mlkl−/− mice, suggesting that an ASC inflammasome-driven mechanism causes lethality in the absence of active caspase 8.

“These studies… describe a previously unknown mechanism for catalytically inactive caspase 8 in triggering the pyroptosis cell death pathway in the absence of apoptosis and necroptosis”

These studies therefore describe a previously unknown mechanism for catalytically inactive caspase 8 in triggering the pyroptosis cell death pathway in the absence of apoptosis and necroptosis. This mechanism could act as a defence against viruses that have evolved strategies to inhibit caspase 8 catalytic activity and parts of the necroptosis machinery.


Original articles

  1. Newton, K. et al. Activity of caspase-8 determines plasticity between cell death pathways. Nature 575, 679–682 (2019)

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  2. Fritsch, M. et al. Caspase-8 is the molecular switch for apoptosis, necroptosis and pyroptosis. Nature 575, 683–687 (2019)

    CAS  Article  Google Scholar 

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Correspondence to Joseph Willson.

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Willson, J. A matter of life and death for caspase 8. Nat Rev Mol Cell Biol 21, 63 (2020).

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