Feeding conditions control the expression of genes involved in sterol metabolism in peripheral blood mononuclear cells of normoweight and diet-induced (cafeteria) obese rats

• Published in: The Journal of nutritional biochemistry Vol. 21; no. 11; pp. 1127 - 1133
• Main Authors: Caimari, Antoni, Oliver, Paula, Rodenburg, Wendy, Keijer, Jaap, Palou, Andreu
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01-11-2010; New York, NY: Elsevier Science; Elsevier
• Subjects: acute regulatory protein; adipose-tissue; Adiposity; Animals; beta-methylglutaryl-coenzyme; Biological and medical sciences; Cafeteria diet; Cholesterol; coa-cholesterol acyltransferase; Diet; Fasting - metabolism; Feeding conditions; Feeding. Feeding behavior; Fundamental and applied biological sciences. Psychology; Gene Expression Profiling; human-lymphocytes; in-vivo; Leukocytes, Mononuclear - metabolism; lipid-synthesis; low-density-lipoprotein; Male; messenger-rna expression; Microarray; Obesity - genetics; Obesity - metabolism; Oligonucleotide Array Sequence Analysis; PBMC; Rats; Rats, Wistar; Reverse Transcriptase Polymerase Chain Reaction; signal-transduction; Sterol metabolism; Sterols - metabolism; Vertebrates: anatomy and physiology, studies on body, several organs or systems; Microarray; Sterol metabolism; PBMC; Feeding conditions; Cafeteria diet; Obesity; Feeding behavior; Rat; Rodentia; Nutrition disorder; Gene expression; Metabolism; Feeding; Vertebrata; Blood cell; Mammalia; Mononuclear cell; Animal; Nutritional status; Sterol
• ISSN: 0955-2863; 1873-4847
• DOI: 10.1016/j.jnutbio.2009.10.001

Peripheral blood mononuclear cells (PBMC) are easily obtainable cells from blood whose gene expression profiles have been proven to be highly robust in distinguishing a disease state from healthy state. Sterol metabolism is of physiological importance, and although its nutritional response in liver has been described, it is poorly studied in PBMC. To examine if PBMC sterol metabolism reflects diet-induced physiological responses, we analysed the whole genome gene expression response of PBMC and focused on sterol metabolism-related genes affected by different feeding conditions (ad libitum feeding, fasting, and refeeding) in normoweight (control) rats and in diet-induced (cafeteria) obese rats.
Our results of microarray analysis show that, in control rats, 21 genes involved in sterol metabolism were regulated by the different feeding conditions, whereas in cafeteria-obese rats, only seven genes showed a changed expression. Most of the genes identified were classified into three pathways: sterol biosynthesis, cholesterol transport and uptake and sterol signaling. The expression profile of these genes was similar to that previously described for liver, decreasing in response to fasting conditions and recovering the levels found in fed animals after 6-h-refeeding. In addition, our data and the comparable expression pattern of sterol metabolism-related genes between PBMC and liver suggest similar sterol regulatory element-binding protein-mediated regulatory mechanisms in response to feeding conditions in both tissues.
In conclusion, the expression of genes involved in sterol metabolism is highly controlled by feeding conditions in PBMC of control rats, but this control is impaired in cafeteria-obese animals. The pathophysiological significance of this impairment requires further investigation.