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中华毛囊被孢霉菌丝通过抑制经典和非经典炎性小体来抑制白细胞介素-1β和白细胞介素-18 的分泌。

Hirsutella sinensis mycelium suppresses interleukin-1β and interleukin-18 secretion by inhibiting both canonical and non-canonical inflammasomes.

机构信息

Center for Molecular and Clinical Immunology, Chang Gung University, Taoyuan, Taiwan, Republic of China.

出版信息

Sci Rep. 2013;3:1374. doi: 10.1038/srep01374.

DOI:10.1038/srep01374
PMID:23459183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3587886/
Abstract

Cordyceps sinensis is a medicinal mushroom used for centuries in Asian countries as a health supplement and tonic. Hirsutella sinensis-the anamorphic, mycelial form of C. sinensis-possesses similar properties, and is increasingly used as a health supplement. Recently, C. sinensis extracts were shown to inhibit the production of the pro-inflammatory cytokine IL-1β in lipopolysaccharide-treated macrophages. However, the molecular mechanism underlying this process has remained unclear. In addition, whether H. sinensis mycelium (HSM) extracts also inhibit the production of IL-1β has not been investigated. In the present study, the HSM extract suppresses IL-1β and IL-18 secretion, and ATP-induced activation of caspase-1. Notably, we observed that HSM not only reduced expression of the inflammasome component NLRP1 and the P2X7R but also reduced the activation of caspase-4, and ATP-induced ROS production. These findings reveal that the HSM extract has anti-inflammatory properties attributed to its ability to inhibit both canonical and non-canonical inflammasomes.

摘要

冬虫夏草是一种药用蘑菇,在亚洲国家被使用了几个世纪,作为一种保健品和滋补品。中华束丝孢菌——冬虫夏草的无性型、菌丝体形式——具有相似的特性,越来越多地被用作保健品。最近,研究表明,冬虫夏草提取物可以抑制脂多糖处理的巨噬细胞中促炎细胞因子 IL-1β的产生。然而,这一过程的分子机制仍不清楚。此外,中华束丝孢菌菌丝体(HSM)提取物是否也能抑制 IL-1β的产生尚未得到研究。在本研究中,HSM 提取物抑制了 IL-1β和 IL-18 的分泌,以及 ATP 诱导的半胱天冬酶-1 的激活。值得注意的是,我们观察到 HSM 不仅降低了炎症小体成分 NLRP1 和 P2X7R 的表达,还降低了半胱天冬酶-4 的激活以及 ATP 诱导的 ROS 产生。这些发现表明,HSM 提取物具有抗炎特性,这归因于其抑制经典和非经典炎症小体的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/1776e3adab83/srep01374-f7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/2a3690fa27d4/srep01374-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/80b13bbb4d69/srep01374-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/f7e875cf6ae4/srep01374-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/1776e3adab83/srep01374-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/4a4c31d80795/srep01374-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/ac75ed95131d/srep01374-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/5891cfe7c122/srep01374-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/2a3690fa27d4/srep01374-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/80b13bbb4d69/srep01374-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/f7e875cf6ae4/srep01374-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf4d/3587886/1776e3adab83/srep01374-f7.jpg

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