Ramirez-Torres 2012 J Proteomics
|Ramirez-Torres A, Barcelo-Batllori S, Fernandez-Vizarra E, Navarro MA, Arnal C, Guillen N, Acin S, Osada J (2012) Proteomics and gene expression analyses of mitochondria from squalene-treated apoE-deficient mice identify short-chain specific acyl-CoA dehydrogenase changes associated with fatty liver amelioration. J Proteomics 75:2563-75.|
Abstract: Squalene, a hydrocarbon involved in cholesterol biosynthesis, is an abundant component in virgin olive oil. Previous studies showed that its administration decreased atherosclerosis and steatosis in male apoE knock-out mice. To study the effect of squalene on mitochondrial proteins in fatty liver, 1g/kg/day of this isoprenoid was administered to those mice. After 10 weeks, hepatic fat was assessed and protein extracts from mitochondria enriched fractions from control and squalene-treated animals were analyzed by 2D-DIGE. Spots exhibiting significant differences were identified by MS analysis. Squalene administration modified the expression of eighteen proteins involved in different metabolic processes, 12 associated with hepatic fat content. Methionine adenosyltransferase I alpha (Mat1a) and short-chain specific acyl-CoA dehydrogenase (Acads) showed significant increased and decreased transcripts, respectively, consistent with their protein changes. These mRNAs were also studied in wild-type mice receiving squalene, where Mat1a was found increased and Acads decreased. However, this mRNA was significantly increased in the absence of apolipoprotein E. These results suggest that squalene action may be executed through a complex regulation of mitochondrial protein expression, including changes in Mat1a and Acads levels. Indeed, Mat1a is a target of squalene administration while Acads reflects the anti-steatotic properties of squalene.
Highlights Squalene (1 g/kg/day) decreased triglycerides in apoE-ko mice hepatocytes. Mitochondrial hepatic proteomic analysis unveiled 18 proteins modified by squalene. Squalene action executes a complex regulation of mitochondrial protein expressions. Squalene-induced decrease in steatosis is related to ACADS and it could be a biomarker. MAT1A is increased by squalene administration.
• Keywords: ApoE knock-out, Squalene, Acads, Mat1a
• O2k-Network Lab: ES Zaragoza Ruiz-Pesini E
Labels: MiParea: Respiration, nDNA;cell genetics, Genetic knockout;overexpression, Exercise physiology;nutrition;life style Pathology: Aging;senescence
Organism: Mouse Tissue;cell: Liver Preparation: Isolated mitochondria