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Human leucine zipper protein promotes hepatic steatosis via induction of apolipoprotein A‐IV
Author(s) -
Kang Minsoo,
Kim Jeonghan,
An HyoungTae,
Ko Jesang
Publication year - 2017
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.201601227r
Subject(s) - steatosis , leucine zipper , chemistry , apolipoprotein b , lipid metabolism , biochemistry , biology , gene , transcription factor , endocrinology , cholesterol
The molecular mechanism of stress‐induced hepatic steatosis is not well known. Human leucine zipper protein (LZIP) regulates the expression of genes involved in inflammation, cell migration, and stress response. The aim of this study was to determine the regulatory role of LZIP in stress‐induced hepatic steatosis. We used a microarray analysis to identify LZIP‐induced genes involved in hepatic lipid metabolism. LZIP increased the expression of apolipoprotein A‐IV (APOA4) mRNA. In the presence of stress inducer, APOA4 promoter analysis was performed, and LZIP‐induced lipid accumulation was monitored in mouse primary cells and human tissues. Under Golgi stress conditions, LZIP underwent proteolytic cleavage and was phosphorylated by AKT to protect against proteasome degradation. The stabilized N‐terminal LZIP was translocated to the nucleus, where it directly bound to the APOA4 promoter, leading to APOA4 induction. LZIP‐induced APOA4 expression resulted in increased absorption of surrounding free fatty acids. LZIP also promoted hepatic steatosis in mouse liver. Both LZIP and APOA4 were highly expressed in human steatosis samples. Our findings indicate that LZIP is a novel modulator of APOA4 expression and hepatic lipid metabolism. LZIP might be a therapeutic target for developing treatment strategies for hepatic steatosis and related metabolic diseases.—Kang, M., Kim, J., An, H.‐T., Ko, J. Human leucine zipper protein promotes hepatic steatosis via induction of apolipoprotein A‐IV. FASEB J. 31, 2548–2561 (2017). www.fasebj.org