Targeting alkaline ceramidase 3 alleviates the severity of nonalcoholic steatohepatitis by reducing oxidative stress.

Abstract

Overload of palmitic acids is linked to the dysregulation of ceramide metabolism in nonalcoholic steatohepatitis (NASH), and ceramides are important bioactive lipids mediating the lipotoxicity of palmitic acid in NASH. However, much remains unclear about the role of ceramidases that catalyze the hydrolysis of ceramides in NASH. By analyzing the National Center for Biotechnology Information (NCBI) Gene Expression Omnibus (GEO) database, we found that alkaline ceramidase 3 (ACER3) is upregulated in livers of patients with NASH. Consistently, we found that Acer3 mRNA levels and its enzymatic activity were also upregulated in mouse livers with NASH induced by a palmitate-enriched Western diet (PEWD). Moreover, we demonstrated that palmitate treatment also elevated Acer3 mRNA levels and its enzymatic activity in mouse primary hepatocytes. In order to investigate the function of Acer3 in NASH, Acer3 null mice and their wild-type littermates were fed a PEWD to induce NASH. Knocking out Acer3 was found to augment PEWD-induced elevation of C18:1-ceramide and alleviate early inflammation and fibrosis but not steatosis in mouse livers with NASH. In addition, Acer3 deficiency attenuated hepatocyte apoptosis in livers with NASH. These protective effects of Acer3 deficiency were found to be associated with suppression of hepatocellular oxidative stress in NASH liver. In vitro studies further revealed that loss of ACER3/Acer3 increased C18:1-ceramide and inhibited apoptosis and oxidative stress in mouse primary hepatocytes and immortalized human hepatocytes induced by palmitic-acid treatment. These results suggest that ACER3 plays an important pathological role in NASH by mediating palmitic-acid-induced oxidative stress.

• Authors: Kai Wang, Chuanjiang Li, Xinxin Lin, Hang Sun, Ruijuan Xu, Qingping Li, Yiran Wei, Yiyi Li, Jianping Qian, Cuiting Liu, Qifan Zhang, Sheng Yu, Zhonglin Cui, Xixin Huang, Bili Zhu, Jie Zhou, Cungui Mao
• Journal: Cell death & disease (Cell Death Dis) Vol. 11 Issue 1 Pg. 28 (01 16 2020) ISSN: 2041-4889 [Electronic] England
• PMID: 31949129 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Palmitic Acid
• ACER3 protein, human
• Acer1 protein, mouse
• Alkaline Ceramidase

Topics

• Alkaline Ceramidase (deficiency, genetics, metabolism)
• Animals
• Apoptosis (genetics)
• Cell Survival (genetics)
• Chromatography, Liquid
• Diet, Western
• Hepatocytes (enzymology, metabolism)
• Humans
• Inflammation (diet therapy)
• Liver (metabolism, pathology)
• Liver Cirrhosis (enzymology, genetics, metabolism)
• Male
• Mice
• Mice, Inbred C57BL
• Mice, Knockout
• Non-alcoholic Fatty Liver Disease (enzymology, genetics, metabolism)
• Oxidative Stress (genetics)
• Palmitic Acid (pharmacology)
• Tandem Mass Spectrometry
• Up-Regulation