脂毒性
脂质代谢
内科学
糖基化
过氧化物酶体增殖物激活受体
内分泌学
化学
新陈代谢
脂质积聚
医学
生物化学
受体
胰岛素抵抗
肥胖
作者
Ning Zhang,Yuli Wang,Junli Zhang,Beibei Liu,Xiaoling Deng,Shengliang Xin,Keshu Xu
标识
DOI:10.1096/fj.202000836rr
摘要
These findings have important implications for the role of CREBH N-glycosylation in proteolytic activation, and they provide the first link between N-glycosylation of CREBH, lipid metabolism, and lipotoxicity processes in the liver by modulating PPARα and SCD-1. These results provide novel insights into the N-glycosylation of CREBH as a therapeutic target for NAFLD.
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