Unknown

Dataset Information

0

Glutathione peroxidase 8 negatively regulates caspase-4/11 to protect against colitis


ABSTRACT: Human caspase-4 and its mouse homolog caspase-11 are receptors for cytoplasmic lipopolysaccharide. Activation of the caspase-4/11-dependent NLRP3 inflammasome is required for innate defense and endotoxic shock, but how caspase-4/11 is modulated remains unclear. Here, we show that mice lacking the oxidative stress sensor glutathione peroxidase 8 (GPx8) are more susceptible to colitis and endotoxic shock, and exhibit reduced richness and diversity of the gut microbiome. C57BL/6 mice that underwent adoptive cell transfer of GPx8-deficient macrophages displayed a similar phenotype of enhanced colitis, indicating a critical role of GPx8 in macrophages. GPx8 binds covalently to caspase-4/11 via disulfide bonding between cysteine 79 of GPx8 and cysteine 118 of caspase-4, and thus restrains caspase-4/11 activation, while GPx8 deficiency leads to caspase-4/11-induced inflammation during colitis and septic shock. Inhibition of caspase-4/11 activation with small molecules reduces the severity of colitis in GPx8-deficient mice. Notably, colonic tissues from patients with ulcerative colitis display low levels of Gpx8 and high caspase-4 expression. In conclusion, these results suggest that GPx8 protects against colitis by negatively regulating caspase-4/11 activity.

SUBMITTER: Dr. Jye-Lin Hsu 

PROVIDER: S-SCDT-EMM-2018-09386 | biostudies-other |

REPOSITORIES: biostudies-other

Similar Datasets

| S-EPMC6949489 | biostudies-literature
| S-EPMC4205216 | biostudies-literature
| S-EPMC6484510 | biostudies-literature
| S-EPMC4298125 | biostudies-literature
| S-EPMC8806340 | biostudies-literature
| S-EPMC3563732 | biostudies-literature
| S-EPMC3419307 | biostudies-literature
| S-EPMC3697099 | biostudies-literature
| S-EPMC2673260 | biostudies-literature
| S-EPMC7236273 | biostudies-literature