Sidt2 regulates hepatocellular lipid metabolism through autophagy

• Published in: Journal of lipid research Vol. 59; no. 3; pp. 404 - 415
• Main Authors: Chen, Xueru, Gu, Xuefan, Zhang, Huiwen
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.2018; Journal of Lipid Research; The American Society for Biochemistry and Molecular Biology; Elsevier
• Subjects: Animals; Autophagy; Electron microscopy; Fatty acids; Fatty liver; Food consumption; Gene expression; Hepatocytes; Hepatocytes - chemistry; Hepatocytes - metabolism; Homeostasis; Image processing; lipid droplets; Lipid Droplets - metabolism; Lipid Metabolism; Lipids; Lipids - analysis; Lipogenesis; Lipolysis; Liver; liver metabolism; Male; Membrane proteins; Membrane Proteins - deficiency; Membrane Proteins - metabolism; Mice; Mice, Knockout; Nucleotide Transport Proteins; Oxidation; Phagocytosis; Rodents; Secretion; SID1 transmembrane family member 2; triglycerides; liver metabolism; triglycerides; SID1 transmembrane family member 2; lipid droplets
• ISSN: 0022-2275; 1539-7262
• DOI: 10.1194/jlr.M073817

SID1 transmembrane family member 2 (Sidt2) is an integral lysosomal membrane protein. To investigate its explicit function, we generated a global Sidt2 knockout mouse model (Sidt2−/−). Compared with the littermate controls, Sidt2−/− mice exhibited a remarkable accumulation of lipid droplets in liver. First, it was observed that food consumption, hepatocyte fatty acid uptake and de novo lipogenesis, hepatocyte lipolysis, and TG secretion in the form of very low density lipoprotein were comparable between Sidt2−/− and WT mice. However, the hepatic β-oxidation of fatty acids decreased significantly as revealed by a low level of serum β-hydroxybutyrate in the Sidt2−/− mice along with normal mRNA expression of genes involved in fatty acid oxidation. In addition, the classical autophagy pathway marker proteins, p62 and LC3-II, increased in liver, along with compromised autophagic flux in primary hepatocytes, indicating a block of autophagosome maturation due to Sidt2 deficiency, which was also supported by electron microscopy image analysis both in livers and in primary hepatocytes from Sidt2−/− mice. It was concluded that Sidt2 plays an important role in mouse hepatic lipid homeostasis by regulating autophagy at the terminal stage.