Journal
CELL REPORTS
Volume 39, Issue 5, Pages -Publisher
CELL PRESS
DOI: 10.1016/j.celrep.2022.110755
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Funding
- NIH [AI119015, AI148491, AI132850]
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CD14 plays a vital role in intracellular LPS sensing by mediating the cytosolic localization of LPS, leading to the activation of caspase-11. This study provides evidence for the critical role of CD14 in noncanonical inflammasome sensing of LPS.
Intracellular lipopolysaccharide (LPS) sensing by the noncanonical inflammasome comprising caspase-4 or -11 governs antibacterial host defense. How LPS gains intracellular access in vivo is largely unknown. Here, we show that CD14-an LPS-binding protein with a well-documented role in TLR4 activation-plays a vital role in intracellular LPS sensing in vivo. By generating Cd14(-/-) and Casp11(-/-) mice strains on a Tlr4(-/-) background, we dissociate CD14's known role in TLR4 signaling from its role in caspase-11 activation and show a TLR4-independent role for CD14 in GSDMD activation, pyroptosis, alarmin release, and the lethality driven by cytosolic LPS. Mechanistically, CD14 enables caspase-11 activation by mediating cytosolic localization of LPS in a TLR4-independent manner. Overall, our findings attribute a critical role for CD14 in noncanonical inflammasome sensing of LPS in vivo and establish-together with previous literature-CD14 as an essential proximal component of both TLR4-based extracellular and caspase-11-based intracellular LPS surveillance.
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