Carcinogenesis, Teratogenesis & Mutagenesis ›› 2019, Vol. 31 ›› Issue (1): 35-40.doi: 10.3969/j.issn.1004-616x.2019.01.006

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Effects of formaldehyde on free cholesterol metabolism in HepG2 cells

JIANG Xuexia, WANG Pan, LIU Yanfei, ZHANG Yan, BAI Jianying   

  1. Department of Environment Health, School of Public Health, Shanxi Medical University, Taiyuan 030001, Shanxi, China
  • Received:2018-10-15 Revised:2018-12-12 Online:2019-01-31 Published:2019-01-31

Abstract: OBJECTIVE:To explore effects of formaldehyde (FA) on intra-hepatocellular free cholesterol content in HepG2 cells. METHODS:HepG2 cells were treated with formaldehyde at 0.004,0.02 and 0.1 mmol/L concentrations for 24 and 48 hours,respectively. The content of intra-hepatocellular free cholesterol was detected by using free the cholesterol GPO-POD assay kit. Western blot was used to detect protein expression of the sterol regulatory element-binding protein (SREBP) -2,hydroxy mothylglutaryl coenzyme A reductase (HMGCR),acyl coenzyme A-cholesterol acyltransferase (ACAT) and low-density lipoprotein receptor (LDLR). RESULTS:Compared with negative control,the contents of intra-hepatocellular FC were increased significantly after treatments with FA for 24 h and 0.02 and 0.1 mmol/L for 48 h (P < 0.05). HMGCR expression levels were significantly increased after exposure to formaldehyde for 24 and 48 h (P < 0.05). After treatment with FA for 24 h,expression levels of ACAT and LDLR were significantly down-regulated (P < 0.05). After 48 h,expression levels of LDLR were decreased significantly,whereas the levels of ACAT were decreased significantly after treatment with 0.02 and 0.1 mmol/L FA (P < 0.05). CONCLUSION:FA exposure increased intra-hepatocellular free cholesterol contents in HepG2 cells. The increase could be caused by elevated de novo synthesis of cholesterol and decreased cholesterol esterification.

Key words: formaldehyde, sterol regulatory element binding protein 2, hydroxy mothylglutaryl coenzyme A reductase, acyl coenzyme A-cholesterol acyltransferase, low-density lipoprotein receptor

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