脂滴包被蛋白
脂滴
化学
下调和上调
细胞生物学
过氧化物酶体
PI3K/AKT/mTOR通路
过氧化物酶体增殖物激活受体
脂质代谢
油酸
内分泌学
内科学
受体
生物化学
脂肪细胞
信号转导
生物
脂肪组织
医学
基因
作者
Wenxia Zhong,Bin Fan,Huiying Cong,Tianyu Wang,Jianqiu Gu
标识
DOI:10.1139/apnm-2018-0729
摘要
Perilipin 5 (Plin5), a member of the PAT (Perilipin, ADRP, and Tip47) protein family, has been implicated in the regulation of cellular neutral lipid accumulation in nonalcoholic fatty liver diseases. However, the underlying regulatory mechanisms of Plin5 are not clear. The goal of the present study was to explore the mechanism of oleic acid (OA)-induced Plin5 expression in HepG2 cells. We found that the expression of Plin5 was increased during OA-induced lipid droplets formation in a dose- and time-dependent manner. During this process of OA-stimulated lipid droplets formation, peroxisome proliferator-activated receptor alpha (PPARα) was also upregulated. When PPARα activation was blocked by GW6471, OA-induced Plin5 expression and lipid droplets formation were effectively ablated. We further found that the phosphoinositide 3-kinase (PI3K) inhibitor LY294002 was able to downregulate both PPARα and Plin5 expression and lipid droplets formation. Thus, we concluded that PI3K may, at least in part, act upstream of PPARα to regulate Plin5 expression and lipid droplets formation in HepG2 cells.
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