Cellular and Molecular Gastroenterology and Hepatology · 2021 · 109 citations · 35 references
Life SciencesBiochemistryCellular BiochemistryLipid BiochemistryMetabolismFatty Acid MetabolismLipid MetabolismLipoprotein MetabolismMetabolic Liver DiseaseTriacylglycerol MetabolismTriglyceride MetabolismHepatic Lipid AccumulationHepatic Lipid SecretionHepatic Lipid StorageHepatic Lipoprotein SecretionNeutral Lipid ContentNeutral LipidsTransmembrane ProteinsTriglyceride Synthesis
BACKGROUND & AIMS: rats to determine the subcellular location and function of TM6SF2. METHODS: mice and in their wild-type littermates. The intracellular location of TM6SF2 was determined by cell fractionation. Finally, TM6SF2 was immunoprecipitated from liver and enterocytes to identify interacting proteins. RESULTS: mice. TM6SF2 was present predominantly in the smooth endoplasmic reticulum and endoplasmic reticulum-Golgi intermediate compartments, but not in Golgi. Both apolipoprotein B-48 and acyl-CoA synthetase long chain family member 5 physically interacted with TM6SF2. CONCLUSIONS: TM6SF2 acts in the smooth endoplasmic reticulum to promote bulk lipidation of apolipoprotein B-containing lipoproteins, thus preventing fatty liver disease.
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Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease
Stefano Romeo, Julia Kozlitina, Chao Xing et al. · Nature Genetics · 2008 · 3.4K citations · Full text