Laboratory of Molecular Biology, Nutrition and Biotechnology, Universitat de les Illes Balears and CIBER de Fisiopatología de la Obesidad y Nutrición (CIBEROBN), E-07122, Palma de Mallorca, Spain.
J Nutr Biochem. 2010 Nov;21(11):1127-33. doi: 10.1016/j.jnutbio.2009.10.001. Epub 2010 Feb 20.
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.
外周血单个核细胞(PBMC)是一种易于从血液中获得的细胞,其基因表达谱已被证明在区分疾病状态与健康状态方面具有高度稳健性。固醇代谢具有生理重要性,虽然已经描述了其在肝脏中的营养反应,但在 PBMC 中的研究甚少。为了研究 PBMC 固醇代谢是否反映饮食引起的生理反应,我们分析了 PBMC 的全基因组基因表达反应,并专注于受不同喂养条件(自由喂养、禁食和再喂养)影响的固醇代谢相关基因,这些喂养条件在正常体重(对照)大鼠和饮食诱导(自助餐)肥胖大鼠中进行。我们的微阵列分析结果表明,在对照大鼠中,21 个参与固醇代谢的基因受不同喂养条件的调节,而在自助餐肥胖大鼠中,只有 7 个基因的表达发生变化。鉴定出的大多数基因分为三个途径:固醇生物合成、胆固醇转运和摄取以及固醇信号。这些基因的表达谱与先前描述的肝脏相似,在禁食条件下降低,在 6 小时再喂养后恢复到进食动物的水平。此外,我们的数据以及 PBMC 和肝脏中固醇代谢相关基因的可比表达模式表明,两种组织中对喂养条件的固醇调节元件结合蛋白介导的调节机制相似。总之,在对照大鼠的 PBMC 中,固醇代谢相关基因的表达受到喂养条件的高度控制,但这种控制在自助餐肥胖动物中受损。这种损伤的病理生理意义需要进一步研究。