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Caspase-8 is involved in pyroptosis, necroptosis and the maturation and release of IL-1β in Aspergillus fumigatus keratitis

上睑下垂 真菌性角膜炎 烟曲霉 坏死性下垂 半胱氨酸蛋白酶1 微生物学 生物 污渍 角膜炎 分子生物学 细胞凋亡 程序性细胞死亡 免疫学 生物化学 遗传学 基因
作者
Limei Wang,Haijing Yan,Xiaomeng Chen,Jieun Lee,Jintao Sun,Guibo Liu,Hua Yang,Danli Lu,Wenting Liu,Chengye Che
出处
期刊:International Immunopharmacology [Elsevier BV]
卷期号:113: 109275-109275 被引量:5
标识
DOI:10.1016/j.intimp.2022.109275
摘要

To explore the role of caspase-8 in mediating the transition between different death modes in fungal keratitis.The expression of caspase-8 in Aspergillus fumigatus (A. fumigatus) keratitis was detected using western blotting and immunofluorescence. After subconjunctival injection of Z-IETD-FMK (caspase-8 inhibitor) or VX765 (caspase-1 inhibitor), the mice corneas of A. fumigatus keratitis were observed and scored under a slit lamp. Colony plate count, immunofluorescence staining, western blotting and qRT-PCR experiments were used to detect fungal load, inflammatory cells, and the production of related mRNAs and proteins. In vitro experiments, the LDH release test, Cell Count Kit-8(CCK-8) assay, ELISA, qRT-PCR and western blotting were used to detect cell viability, related mRNAs and proteins.The caspase-8 protein was upregulated following fungal infection. Compared with the A. fumigatus keratitis group, the mice treated with Z-IETD-FMK had heavier corneal turbidity, higher clinical scores, more fungal load and fewer inflammatory cells. The expression of NLRP3, cleaved-caspase-1, N-GSDMD, and IL-1β in the fungal infection group after Z-IETD-FMK pretreatment were downregulated, while RIPK3 and p-MLKL were upregulated. In the fungal infection group after VX765 pretreatment, the expression of cleaved-caspase-8 was up-regulated, while N-GSDMD was downregulated.Caspase-8 is involved in the early immune defense response of A. fumigatus keratitis. It is essential for the recruitment of inflammatory cells and the clearance of the fungus. In A. fumigatus keratitis, activated caspase-8 promoted the caspase-1/GSDMD signaling pathway to participate in pyroptosis, inhibited RIPK3/MLKL signaling pathway-mediated necroptosis, and promoted IL-1β maturation and release by activating the NLRP3 inflammasomes.
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