Abstract
Plasma low-density lipoprotein-cholesterol (LDL-C) is mainly taken up and cleared
by the hepatocellular LDL receptor (LDL-R). LDL-R gene expression is regulated by
the sterol regulatory element binding proteins (SREBPs). Previous studies have shown
that curcumin reduces plasma LDL-C and has hypolipidemic and anti-atherosclerotic
effects. Herein, we investigated the effect of curcumin on LDL-R expression and its
molecular mechanism in HepG2 cells. Curcumin increased LDL-R expression (mRNA and
protein) and the resultant uptake of DiI-LDL in a dose- and time-dependent manner.
Using a GFP reporter system in a transfected HepG2/SRE-GFP cell line, we found that
curcumin activated the sterol regulatory element of the LDL-R promoter. In HepG2/Insig2
cells, curcumin reversed the inhibition of LDL-R expression induced by Insig2 overexpression.
These data demonstrate that curcumin increases LDL-R protein expression and uptake
activity via the SREBPs pathway. These findings contribute to our further understanding
of the cholesterol-lowering and anti-atherosclerotic effects of curcumin.
Key words
curcumin - Curcuma longa L. - Zingiberaceae - low-density lipoprotein receptor - SREBP
- HepG2
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Prof. Chunlei Fan
Life Science College of Zhejiang Chinese Medical University
Binwen Road 548#
Hangzhou 310053
Zhejiang Province
People’s Republic of China
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