3-ketodihydrosphingosine reductase mutation induces steatosis and hepatic injury in zebrafish

• Published in: Scientific reports Vol. 9; no. 1; p. 1138
• Main Authors: Park, Ki-Hoon, Ye, Zhi-Wei, Zhang, Jie, Hammad, Samar M, Townsend, Danyelle M, Rockey, Don C, Kim, Seok-Hyung
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 04.02.2019; Nature Publishing Group UK
• Subjects: Alcohol Oxidoreductases - genetics; Alcohol Oxidoreductases - metabolism; Animals; Cristae; Danio rerio; Disease Models, Animal; Endoplasmic Reticulum Stress; Fatty liver; Fatty Liver - genetics; Fatty Liver - metabolism; Genetic analysis; Hepatocytes; Humans; Kinases; Lipidomics - methods; Mitochondria; Mitochondria - metabolism; Mitochondria - ultrastructure; Mutants; Mutation; Mutation, Missense; Oxidative Stress; Phenotypes; Phosphotransferases (Alcohol Group Acceptor) - genetics; Phosphotransferases (Alcohol Group Acceptor) - metabolism; Reductase; Risk factors; Sphingolipids; Sphingolipids - metabolism; Sphingosine 1-phosphate; Sphingosine kinase; Steatosis; Up-Regulation; Zebrafish; Zebrafish Proteins - genetics; Zebrafish Proteins - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-37946-0

3-ketodihydrosphingosine reductase (KDSR) is the key enzyme in the de novo sphingolipid synthesis. We identified a novel missense kdsr mutation in zebrafish that led to a loss of function, and resulted in progression of hepatomegaly to steatosis, then hepatic injury phenotype. Lipidomics analysis of the kdsr mutant revealed compensatory activation of the sphingolipid salvage pathway, resulting in significant accumulation of sphingolipids including ceramides, sphingosine and sphingosine 1-phosphate (S1P). Ultrastructural analysis revealed swollen mitochondria with cristae damage in the kdsr mutant hepatocytes, which can be a cause of hepatic injury in the mutant. We found elevated sphingosine kinase 2 (sphk2) expression in the kdsr mutant. Genetic interaction analysis with the kdsr and the sphk2 mutants showed that sphk2 depletion suppressed liver defects observed in the kdsr mutant, suggesting that liver defects were mediated by S1P accumulation. Further, both oxidative stress and ER stress were completely suppressed by deletion of sphk2 in kdsr mutants, linking these two processes mechanistically to hepatic injury in the kdsr mutants. Importantly, we found that the heterozygous mutation in kdsr induced predisposed liver injury in adult zebrafish. These data point to kdsr as a novel genetic risk factor for hepatic injury.