Lentinan from shiitake selectively attenuates AIM2 and non-canonical inflammasome activation while inducing pro-inflammatory cytokine production
- Authors
- Ahn, Huijeong; Jeon, Eunsaem; Kim, Jin-Chul; Kang, Seung Goo; Yoon, Sung-il; Ko, Hyun-Jeong; Kim, Pyeung-Hyeun; Lee, Geun-Shik
- Issue Date
- 2017-05-02
- Publisher
- NATURE PUBLISHING GROUP
- Citation
- SCIENTIFIC REPORTS, v.7
- Abstract
- Lentinan extracted from shiitake (Lentinula edodes) is a beta-glucan that has been reported as an intravenous anti-tumor polysaccharide via enhancement of the host immune system. In this study, we determined the effect of lentinan on inflammasome activation, a multi-protein platform, in myeloid cells. Mouse bone marrow-derived macrophages were treated with lentinan with/without inflammasome triggers, and maturation of interleukin (IL)-1 beta, IL-18, or caspase-1 was measured as a readout of inflammasome activation. As a result, lentinan selectively inhibited absent in melanoma 2 (AIM2) inflammasome activation. In addition, lentinan up-regulated pro-inflammatory cytokines and induced expression of inflammasome-related genes through toll-like receptor 4 signaling. Furthermore, we assessed the effect of lentinan on mice treated with Listeria monocytogenes or lipopolysaccharide as an AIM2 or non-canonical inflammasome-mediated model. Lentinan attenuated IL-1 beta secretion resulting from Listeria-mediated AIM2 inflammasome activation and reduced endotoxin lethality via inhibition of non-canonical inflammasome activation. Thus, lentinan is suggested as an anti-AIM2 and anti-non-canonical inflammasome candidate despite its up-regulation of cytokine expression.
- Keywords
- NLRP3 INFLAMMASOME; CELL-PROLIFERATION; IN-VITRO; KAPPA-B; MACROPHAGES; MECHANISM; INFECTION; PROTEINS; NLRC4; NLRP3 INFLAMMASOME; CELL-PROLIFERATION; IN-VITRO; KAPPA-B; MACROPHAGES; MECHANISM; INFECTION; PROTEINS; NLRC4; Lentinan; AIM2; Inflammation; IL-1; caspase-1
- ISSN
- 2045-2322
- URI
- https://pubs.kist.re.kr/handle/201004/122757
- DOI
- 10.1038/s41598-017-01462-4
- Appears in Collections:
- KIST Article > 2017
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