炎症体
吡喃结构域
自噬
免疫印迹
顺铂
半胱氨酸蛋白酶1
下调和上调
化学
肝损伤
药理学
癌症研究
细胞生物学
受体
细胞凋亡
医学
生物
生物化学
内科学
基因
化疗
作者
Xiaoyu Qu,Huan Gao,Lina Tao,Yueming Zhang,Jinghui Zhai,Yanqing Song,Sixi Zhang
摘要
Abstract The nucleotide‐binding oligomerization domain‐like receptor family, pyrin domain containing 3 (NLRP3) inflammasome has a key role in the inflammatory response. We found that cisplatin (7.5, 15 mg/kg, IV) could induce acute injury to the liver and kidneys of rats. Western blot and immunohistochemical analyses showed that expression of NLRP3, caspase‐1 and interleukin‐1β was upregulated significantly in a dose‐dependent manner after cisplatin exposure. Autophagy could inhibit NLRP3 expression and assembly of the NLRP3 inflammasome. Expression of light chain 3 II/I and p62 suggested that autophagy was inhibited during injury to the liver and kidneys. These data suggested that cisplatin might activate NLRP3 by inhibiting autophagy in the liver and kidneys of rats.
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