炎症体
自噬
安普克
锡尔图因
线粒体生物发生
蛋白激酶A
西妥因1
医学
细胞生物学
炎症
生物
激酶
线粒体
免疫学
下调和上调
生物化学
细胞凋亡
NAD+激酶
酶
基因
作者
Mario D. Cordero,Matthew Williams,Bernhard Ryffel
标识
DOI:10.1016/j.tem.2017.10.009
摘要
The NLRP3 inflammasome has recently emerged as an unexpected marker of stress and metabolic risk and has also been implicated in the development of major aging-related diseases such as gout, type 2 diabetes, obesity, cancer, and neurodegenerative and cardiovascular disorders. Several pathways regulating the NLRP3 inflammasome are currently being studied, but how the NLRP3 inflammasome is regulated remains unknown. AMP-activated protein kinase (AMPK), a central regulator of multiple metabolic pathways involved in the pathophysiology of aging and age-related diseases, has emerged as an important integrator of signals controlling inflammation including the inflammasome. In this Opinion article, we show that several AMPK-dependent pathways regulate NLRP3 inflammasome activation during aging, suggesting NLRP3 as a potential pharmacological target in age-related diseases.
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