上睑下垂
顺铂
炎症体
细胞生物学
化学
下调和上调
TXNIP公司
耳蜗
半胱氨酸蛋白酶1
污渍
癌症研究
生物
医学
生物化学
神经科学
内科学
氧化应激
化疗
受体
基因
硫氧还蛋白
作者
Wei Yu,Shimin Zong,Peng Zhou,Jiahui Wei,Enhao Wang,Ruijie Ming,Hongjun Xiao
标识
DOI:10.3389/fimmu.2022.823439
摘要
Better understanding the mechanism of cisplatin-induced ototoxicity is of great significance for clinical prevention and treatment of cisplatin-related hearing loss. However, the mechanism of cisplatin-induced inflammatory response in cochlear stria vascularis and the mechanism of marginal cell (MC) damage have not been fully clarified. In this study, a stable model of cisplatin-induced MC damage was established in vitro, and the results of PCR and Western blotting showed increased expressions of NLRP3, Caspase-1, IL-1β, and GSDMD in MCs. Incomplete cell membranes including many small pores appearing on the membrane were also observed under transmission electron microscopy and scanning electron microscopy. In addition, downregulation of NLRP3 by small interfering RNA can alleviate cisplatin-induced MC pyroptosis, and reducing the expression level of TXNIP possesses the inhibition effect on NLRP3 inflammasome activation and its mediated pyroptosis. Taken together, our results suggest that NLRP3 inflammasome activation may mediate cisplatin-induced MC pyroptosis in cochlear stria vascularis, and TXNIP is a possible upstream regulator, which may be a promising therapeutic target for alleviating cisplatin-induced hearing loss.
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