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A novel pathway of LPS uptake through syndecan-1 leading to pyroptotic cell death.


ABSTRACT: Intracellular lipopolysaccharide (LPS) triggers the non-canonical inflammasome pathway, resulting in pyroptosis of innate immune cells. In addition to its well-known proinflammatory role, LPS can directly cause regression of some tumors, although the underlying mechanism has remained unknown. Here we show that secretoglobin(SCGB)3A2, a small protein predominantly secreted in airways, chaperones LPS to the cytosol through the cell surface receptor syndecan-1; this leads to pyroptotic cell death driven by caspase-11. SCGB3A2 and LPS co-treatment significantly induced pyroptosis of macrophage RAW264.7 cells and decreased cancer cell proliferation in vitro, while SCGB3A2 treatment resulted in reduced progression of xenograft tumors in mice. These data suggest a conserved function for SCGB3A2 in the innate immune system and cancer cells. These findings demonstrate a critical role for SCGB3A2 as an LPS delivery vehicle; they reveal one mechanism whereby LPS enters innate immune cells leading to pyroptosis, and they clarify the direct effect of LPS on cancer cells.

SUBMITTER: Yokoyama S 

PROVIDER: S-EPMC6286126 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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A novel pathway of LPS uptake through syndecan-1 leading to pyroptotic cell death.

Yokoyama Shigetoshi S   Cai Yan Y   Murata Miyuki M   Tomita Takeshi T   Yoneda Mitsuhiro M   Xu Lei L   Pilon Aprile L AL   Cachau Raul E RE   Kimura Shioko S  

eLife 20181207


Intracellular lipopolysaccharide (LPS) triggers the non-canonical inflammasome pathway, resulting in pyroptosis of innate immune cells. In addition to its well-known proinflammatory role, LPS can directly cause regression of some tumors, although the underlying mechanism has remained unknown. Here we show that secretoglobin(SCGB)3A2, a small protein predominantly secreted in airways, chaperones LPS to the cytosol through the cell surface receptor syndecan-1; this leads to pyroptotic cell death d  ...[more]

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