Dihydromyricetin reduces lipid accumulation in LO2 cells via AMPK/mTOR-mediated lipophagy pathway and inhibits HepG2 cell proliferation in vitro.
10.12122/j.issn.1673-4254.2022.04.07
- Author:
Xiao Shan LIAO
1
;
Yu Ting HAO
1
;
Meng Ting WU
1
;
Hui Ping LIU
2
;
Liang JIANG
2
;
Zi Chong YE
1
;
Wen Zhen LIAO
1
;
Hong DENG
1
Author Information
1. Department of Nutrition and Food Hygiene, School of Public Health, Southern Medical University, Guangzhou 510515, China.
2. ERA (Shenzhen) Biotechonology, Shenzhen 518000, China.
- Publication Type:Journal Article
- Keywords:
AMPK/mTOR;
dihydromyricetin;
lipophagy;
nonalcoholic fatty liver disease;
proliferation inhibition
- MeSH:
AMP-Activated Protein Kinases/metabolism*;
Autophagy;
Beclin-1;
Cell Proliferation;
Flavonols;
Hep G2 Cells;
Humans;
Lipids;
RNA, Messenger;
Signal Transduction;
TOR Serine-Threonine Kinases/metabolism*
- From:
Journal of Southern Medical University
2022;42(4):518-527
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the mechanism underlying the hepatoprotective effect of dihydromyricetin (DMY) against lipid accumulation in light of the lipophagy pathway and the inhibitory effect of DMY on HepG2 cell proliferation.
METHODS:LO2 cells were cultured in the presence of 10% FBS for 24 h and treated with 100 μg/mL DMY, or exposed to 50% FBS for 24 h followed by treatment with 50, 100, or 200 μg/mL DMY; the cells in recovery group were cultured in 50% FBS for 24 h and then in 10% FBS for another 24 h. Oil red O staining was used to observe the accumulation of lipid droplets in the cells, and the levels of TC, TG, and LDL and activities of AST, ALT and LDH were measured. The expression of LC3 protein was detected using Western blotting. AO staining and transmission electron microscopy were used to determine the numbers of autophagolysosomes and autophagosomes, respectively. The formation of autophagosomes was observed with MDC staining, and the mRNA expression levels of LC3, ATG7, AMPK, mTOR, p62 and Beclin1 were determined with q-PCR. Flow cytometry was performed to analyze the effect of 50, 100, and 200 μg/mL DMY on cell cycle and apoptosis of HepG2 cells; DNA integrity in the treated cells was examined with cell DNA fragmentation test.
RESULTS:DMY treatment and pretreatment obviously inhibited lipid accumulation and reduced the levels of TC, TG, LDL and enzyme activities of AST, ALT and LDH in LO2 cells (P < 0.05). In routinely cultured LO2 cells, DMY significantly promoted the formation of autophagosomes and autophagolysosomes and upregulated the expression of LC3 protein. DMY obviously attenuated high FBS-induced inhibition of autophagosome formation in LO2 cells, up- regulated the mRNA levels of LC3, ATG7, Beclin1 and AMPK, and downregulated p62 and mTOR mRNA levels (P < 0.05 or 0.01). In HepG2 cells, DMY caused obvious cell cycle arrest, inhibited cell proliferation, and induced late apoptosis and DNA fragmentation.
CONCLUSION:DMY reduces lipid accumulation in LO2 cells by regulating the AMPK/ mTOR-mediated lipophagy pathway and inhibits the proliferation of HepG2 by causing cell cycle arrest and promoting apoptosis.
